2015 Group Project 6

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2015 Student Projects 
2015 Projects: Three Person Embryos | Ovarian Hyper-stimulation Syndrome | Polycystic Ovarian Syndrome | Male Infertility | Oncofertility | Preimplantation Genetic Diagnosis | Students
2015 Group Project Topic - Assisted Reproductive Technology
This page is an undergraduate science embryology student and may contain inaccuracies in either description or acknowledgements.

Prenatal Genetic Diagnosis


Simplified steps for PGD


Prenatal diagnosis was historically conducted post-implantation in the first 2 trimesters [1], testing for overall fetal growth, complications of pregnancy, birth defects as well as chromosomal or genetic abnormalities[2]. Due to advancements in Artificial Reproductive Technologies ( ART) in the past 2 decades , these genetic tests are now conducted as a part of Preimplantation Genetic Diagnosis (PGD) [3] and art used to eliminate the rsik of passing on a genetic disorder to an offspring, before implantation, it ha now become a preventative measure. . In 1990 Preimplantation genetic testing was first used in 1990 on humans to diagnose recessive X-linked diseases in the embryos of pregnant women undergoing IVF. [4] PGD is offered as an alternative to prenatal diagnosis in detecting genetic disorders in high risk couples [5] and avoid passing an inherited disease to the offspring, by selecting genetically "normal" embryos for implantation ,to give the best chance of successful implantation , stable pregnancies and healthy children. [6]

Preimplantation Genetic Diagnosis

Preimplantation genetic diagnosis (PGD) is used to test the genetic makeup of embryos to detect single gene disorders, chromosomal abnormalities and mitochondrial disorders. It also has applications in gender selection for diseases with unequal gender distributions [7]. Some diseases commonly involved with PGD include cystic fibrosis, spinal muscular atrophy and beta – thalassaemia [8] [9]. It was first used in the United Kingdom in the 1980s of arenoleucodystrophy and primarily focusing on sex- linked disorders [9][10]. PGD is now capable of detecting single cell defects (molecular) and chromosomal disorders resulting from the inversion, translocation or deletion of chromosomes (cytogenic) [8],[11]. PGD can be applied to the embryo at different stages. That is on polar bodies, blastomeres or blastocyst [8]. Depending on the type of genetic disorder, PGD utilises different methods of genetic testing. These include Fluorescence in situ hybridisation (FISH) which is used for sex – linked disorders and detects chromosomal rearrangements [11][12] and Embryo halotyping which allows the identification of chromosomes causing the inherited disorder through knowledge of the pattern of closely linked markers [8]. Polymerase chain reaction (PCR) is also widely used to detect molecular abnormalities [11]. PGD is tightly regulated and supported by large organisations namely The American Society for Reproductive Medicine, The European Society for Human Reproduction and Embryology (ESHRE), The European Society of Human Genetics and the Preimplantation Genetic Diagnosis International Society [13].

Sex-linked disorders

The determination of a disease as gender specific usually correlates with the presence or absence of specific genes such as SRY on the Y chromosome. It is known that females have two X chromosomes and males have an X and a Y chromosome where abnormalities are more prevalent on the X chromosome. PGD can be used for sex selection where only male embryos are transferred to reduce the chance of inheriting X-linked disorders. However, this does not completely eradicate the problem as male embryos remain susceptible to inheriting an affected X chromosome. Sex determination is only used when the specific mutation is unknown and has yet to be discovered [14].

Single gene defects

Single gene defects can be dominant, recessive, autosomal or X-linked. They are commonly diagnosed using PCR and although the PCR available today is complex and capable of combatting a large range of disease the development of new protocols has been proven to be difficult due to the small DNA sample available [15]

Mitochondrial disorders

Mitochondrial disorders also known as oxidative phosphorylation disorders arise from mutations in the nuclear DNA or mitochondrial DNA [16]. They pose as a problem because they are unrecognisable until the mutations in the cell reach a detrimental level [7]. Mitochondrial disorders cause miscarriages and stillbirths as well as death in children and young adults. The effects can either be contained in a single organ or more commonly involve multiple organ failure where organs with high energy demands such as the brain, liver muscle and heart and heavily influenced. They are usually occur spontaneously or result from inheritance from the mother. Since mitochondria are solely inherited from the mother oocyte donations have been used as a solution to combat mitochondrial disorders. Additionally, there has been an increasing use in PGD where embryos that stay under the given threshold of 18% gene-mutations are allowed to be transferred and result in normal development. New technology in the areas of nuclear gene transfer and genome editing are also being experimented with [16].

Chromosomal disorders

Chromosomal disorders can be reciprocal, Robertsonian translocations, inversions, deletions and insertions [15]. . Data from ESHRE collected between 2010 and 2011 has shown that the most common chromosomal abnormality confronted in PGD are reciprocal chromosomal abnormalities [17]. PGD has also been used successfully for Robertsonian translocations (RT), a type of structural translocation. Children who carry RT are phenotypically normal, however in their later years it is found that they will suffer from infertility and repeated miscarriages due to the high frequency of abnormal embryos [18]. PCR and FISH are the two main techniques used for chromosomal disorders. To be able to conduct the examinations the cells are required to be at the metaphase stage [15].

Preimplantation Genetic Screening

Prenatal Genetic Screening (PGS) involves an array of methods or ideas that aim to segregate embryos that have genetic flaws and those that are healthy [8]. The occurrence of aneuploidy is high around the stages of early embryonic development and they are the most common cause if miscarriages and congenital birth defects [19]. They have little effect on the morphology of the embryo making them difficult to identify thus identification heavily relies on genetic testing [8]. Genetic sampling is most commonly conducted using Microarray Comparative Genomic Hybridisation (aCGH) as well as FISH, Quantitative PCR and Single Nucleotide Polymorphism (SNP) [8]. These methods collectively aim to assess numeral and structural chromosomal errors [19]. Studies have also introduced Next- Generation Sequencing (NGS) [19] and Whole Genome Amplification used to screen imbalances in the complete 24-chromosomes [20] Statistics from ESHRE have shown that the most common indications for PGS is advanced age, followed by repeated implantation failure or recurrent miscarriage and male infertility [21].


A low percentage of structural abnormalities in chromosomes are responsible for the cause of miscarriages. Despite this, they are the most prevalent type of chromosomal abnormality accounted for in PGD [7]. The presence of specific gene cycles, initiation of embryonic protein synthesis and evident physiological development are all indicative of a successful in vitro fertilisation procedure [22]. To eliminate further errors from occurring during the PGD procedure it is recommended to undertake further prenatal testing such as amniocentesis in the later stages [7].

Advanced maternal age

Data provided by the ESHRE has shown that the mean age of women undergoing PGS is 39 years [21]. Women of advanced age have been shown to have a lower rate of pregnancies reaching childbirth [23]. The highlighted concern revolves around the increased occurrence of aneuploidy following maternal age. The optimal age range for the lowest aneuploidy incidence was found to be between 27 to 37 years of age (6%) then progressively higher in women aged up to 42 (33%) and most common in those 44 and above (53%) [24].

Recurrent pregnancy loss / IVF failure

Recurrent pregnancy loss is defined as three or more IVF failures after cumulative transfer of more than 10 good-quality embryos. These are primarily caused by two main factors, reduced endometrium receptivity or embryonic defects. Endometrium receptivity can be negatively influences by instances including uterine pathologies such as thin endometrium, altered expression of adhesive molecules and immunological factors. Additionally, embryonic defects may be due to genetic abnormalities, embryonic aneuploidy or zona hardening. Endometriosis and hydrosalpinx has been known to effect both the endometrium and embryo [25].

Human leukocyte antigen matching

First used in 2001, HLA matching is an option given to parents to save a child with haematological or immunological disease through conceiving another child who would potentially be able to donate cord blood or haematopoietic stem cells from the bone marrow for transplantation. The process namely PGD-HLA has shown to improve haematopoietic stem cell transplant (HSCT). PGD-HLA can only be performed when HSCT is not needed urgently due to the time needed to conceive and delivery the baby [13]. It is most commonly applied to children suffering from relapsed leukaemia [26]. In a case study PGD-HLA was proven to successfully cure 10 diseases including Fanconi anaemia, Diamond-Blackfan anaemia and beta thalassemia [27].

Biopsy Methods

Biopsy, the removal of genetic materials, from oocytes or embryos in the preimplantation stage is the primary step in PGD. For the past two decades these biopsies have been performed at three stages, the polar body, blastomere, and blastocyst, and the methodologies optimized to ensure the embryo’s viability. The most common approach involves biopsies at the cleavage stage. However, polar body and blastocyst biopsies are increasingly more often tested and applied. Approached for opening the zona pellucida involve next to the traditional mechanical and chemical means, novel approaches such as noncontact lasers. Their application may simplify and secure the procedure significantly. The most challenging question about PGD procedures remains at what stage biopsies should be taken. Much controversy has developed around this topic, highlighting the varying disadvantages and advantages of temporal biopsies. [28]

Time of Biopsy Advantages Disadvantages
Polar Body Day 1 No harm to oocyte Only maternal DNA is tested, often needs to be coupled with other biopsies
Blastomere Day 3
Trophectoderm Day 5 and 6 Little harm, large amount of genetic material Opening of blastocyst necessary, small time window for procedure

Polar body (A), blastomere (B) and trophectoderm (C) biopsies[29].

PMID 24305177

Polar Body Analysis

Day 1


Polar body (PB) biopsy, which was introduced in 1990, offers a promising alternative to biopsies performed at the blastomere stage for PGD/S indications on legal and practical grounds. Description: Consequent embryo development does not necessitate the presence of the first and second PB and their removal may not be crucial. PB biopsy requires precise timing. Keeping track of the meiotic cell cycle is necessary to perform a successful biopsy and, therefore, PB biopsy usually is applied in combination with intracytoplasmic sperm injection (ICSI). During the maturation from the germinal vesicle stage to the metaphase-II stage the first PB is formed. A cytoplasmic bridge containing spindle remnants, that are still in contact with the cellular genetic material, links this PB to the oolemma for about 90 minutes after extrusion. It is possible to visualize these remnants by polarization microscopy and it is crucial to not perform the biopsy until the first PB is no longer firmly attached to the oolemma as this indicates an immature embryo.The oocyte tolerates mechanical zona dissection best during hours four until six after ICSI as the oolemma has stabilized by that time because of the cortical granule reaction. Over time the first PB degenerates stressing a temporal biopsy and its optimal extraction time window is four to 12 hours after ICSI. The second PB forms around two to four hours after ICSI. However, its optimal time window for biopsy is set to be eight to 16 hours after ICSI. This is due to the second PB being attached to the oolemma with spindle remnants until six hours after ICSI. Biopsy at this point may cause enucleation of the oocyte. In addition, studies have shown that the amplification efficiency of second PB’s DNA is worse if the PB is extracted prior to eight hours after ICSI. Thus, it is possible to perform sequential and simultaneous biopsies for the first and second PB. If performed, sequentially the first PB may be removed four to 12 hours and the second PB eight to 16 hours after ICSI. The optimal time window for a biopsy for both the first and second PB simultaneously is eight to 12 hours after ICSI. It is highly preferred to analyze both PBs due to potential aneuploidies in either PB and crossing overs during meiosis[28].


Chemical opening achieved with for example acidic tyrode’s solution of the zona pellucida is not tolerated by the oocyte and may have detrimental effects on the embryo’s development. Therefore, the access to the perivitelline space of the oocyte is provided by mechanical zona dissection or by laser. Both techniques work well if performed by experienced embryologist. However, laser-assisted biopsy is less time consuming when compared to manual dissection. It is critical to consider the size of the introduced opening as it will remain permanent. If it is too large the blastomere may be lost during embryo development and if it is too small it may interfere with hatching of the embryo during blastocyst stage[28]

The presence of a faint but clearly identifiable strand connecting PB2 to the oolemma. The biopsy was performed ∼9 h after ICSI[30].

Laser-assisted polar body biopsy[31]

Advantages & Disadvantages

PB biopsies can only investigate the maternal contributions to the embryo as they are of maternal origin. Thus, this procedure is appropriate for PGD solely for monogenetic diseases from the maternal side. Recessive diseases may be evaluated with PB biopsies on the basis that the embryo’s outcome will be determined by the paternal contribution. (...) It may still be applied for PGS as most aneuploidies either arise during meiosis or origin from the maternal genome. However, diagnosis error has been reported due to the lack of considering paternal contributions. Because PB biopsies are performed very early it is not yet known whether the oocyte will develop into a viable embryo. Thus, PBs are commonly frozen or fixed after biopsy and depending on the state of the embryo only chosen PBs will be tested. This is primarily an economic issue as many genetic testing procedures are very cost-intensive[28].

The sustained implantation predictive value (with 95 % confidence interval) of a euploid screening result obtained from the first polar body (PB1), PB1 and the second polar body (PB2), or a direct embryo biopsy for each stage of embryo transfer (cleavage-stage and blastocyst stage)[32].

Blastomere biopsy

Day 3


Blastomere biopsy has been the prevalent method for PGD and PGS in the last two decades. At least one, but up to two, blastomeres are biopsied on day three of the cleavage stage embryo. The right number of blastomeres removed is a controversial topic as two cells allow for more genetic material and more accurate results. However, removing two cells might be too invasive and damaging to the embryo. (Study)[33]


Initially a hole was drilled into the zona pellucida using acid tyrodes and the blastomeres are removed via aspiration with a pipette[33].

Aspiration of a Blastomere into the biopsy pipette[34].

Laser-assisted blastomere biopsy[35]

Advantages & Disadvantages

Trophectoderm biopsy

Day 5 and 6


The improvement of embryo culture media allowed the in vitro development of human embryos until the blastocyst stage and opened up the possibility to take blastocyst biopsies. During day three to day five the haploid maternal and paternal genomes work together for the first time to form the genome of the embryo. The maternal epigenetic control lessens significantly while preparing for implantation with precisely arranged events happening. The first event includes a rapid increase in the number of embryonic cells which are active in mitotic divisions and apoptosis of aberrant cells. This is followed by the formation of blastocoel (cavitation) which results from the flattening of cell located on the outside of the blastomere. Now the blastocyst will expand until the embryo hatches by rupturing the zona pellucida. The cells of the blastocyst will differentiate to form two distinct cell lineages, the outer trophectoderm and the inner cell mass[28].


Trophectoderm biopsy is usually performed in Hepes buffered biopsy medium and opening approaches include needle cutting which has been replaced by lasers in past years. Different research groups report different timings of the opening to be the most successful. Some open the blastocyst on day three or four by creating a 25 µm which causes the trophectoderm to herniate through this hole and is, thus, accessible for biopsy. Others create this hole about four hours before biopsy which allows sufficient herniation of trophectoderm cells. It is also possible to open the blastocyst immediately before biopsy. This avoids an extra step and the inner cell mass usually is easy to locate. Blastocyst biopsies involve the removal of trophectoderm cells and the ideal time for the procedure is day five. Successful biopsies on day six have been performed, while little is known about the results of biopsies on day seven. However, since the window of implantation in humans is from day eight to ten after ovulation, day seven biopsies appear to be possible[28]. -collapse of trophoblasts -possible: biopsy of hatched blastocyst, holding pipette careful mild suction force to hold embryo near ICM -Cryopreservation

(A) Some trophectoderm cells in a blastocyst started to hatch and (B) the trophectoderm cells were biopsied with assisted laser cutting. Images in C–D show the blastocysts after vitrification and warming. Blastocysts had been cultured for 2–4 hrs after warming, showing good (ICM and trophectoderm cells) hatched (C) and hatching (D) blastocysts. The hatching blastocyst in (E) has good ICM but fair trophectoderm while the blastocyst in (F) has both fair ICM and trophectoderm. Arrows indicate ICMs and arrow heads indicate trophectoderm cells. Bar = 40 µm[36].

Laser-assisted blastocyst biopsy (at 00:50 min)[37]

Advantages & Disadvantages

Blastocyst biopsies are believed to be less damaging to the embryo and appear to be unrelated to implantation rates. In addition, this biopsy method allows for a larger extraction of cells for genetic testing. However, since they are performed late in in vitro development, the time window for genetic testing is relatively small. Fast and accurate genetic testing methods are needed to ensure a successful and safe result from this biopsy. Thus, blastocyst biopsies may gain more popularity in the future whn such methods have been developed or improved[28].

Genetic Techniques



Polymerase chain reaction (PCR) amplifies DNA specific to genetic sequence of interest . PCR was developed by Kay Mullis in the 1980s, for which he was awarded the Nobel prize for chemistry in 1993. [38] This technique enables clinicians to monitor and diagnose diseases using minute samples such as embryonic cells, blood & tissue. [39] PCR has many important applications like DNA fingerprinting, genetic mapping, detection of viruses and bacteria as well as being used to detect genetic disorders, as a part of PGD, in conjunction with IVF. It is used to detect molecular abnormalities such as single gene disorders like Tay Sach, Cycstic fibrosis, Duchenne Muscular Dystrophy, Thalassemia, Huntington disease, Spinal muscular atrophy and many more. Molecular and Genetic analysis require a significant amount of DNA, which we would not have without PCR. It revolutionized the study of DNA, replacing all previous recombinant DNA technology. [40]


Sample are obtained from the the blastocyst, a polar body biopsy or the blastomeres stages of the embryo. Stage 1 Denaturing: separating the target strands of DNA The obtained sample is heated to roughly 90 degrees celcius, this heat causes breaks the relatively weak bonds between nucleotides that form DNA. the double stranded DNA to split into 2 single strands of DNA that are used as templates. Stage 2 Annealing: Binding the Primers to the target DNA sequence PCR will only copy the target sequence of DNA specified by specific PCR primer. These synthesized primers Oligonucleotides are small artificial pieces of DNA. TAQ polymerase enzyme synthesize 2 new strands of DNA duplicate to the single sample DNA stand template indicated by these primers. During this stage the reaction is cooled to a temperature between 40-60 degrees Celsius. Stage 3- Extension- making copies Each of these 2 copies are then used again as templates generating 2 further replications This cycle can occur as many 30 -40 times within a couple hours leading to billions of extra copies of the original DNA segment. The optimal temperature for the further replication is roughly 72 degrees Celsius.

This process mediated by a thermocycler machine that is programmed to alter the temperature of the reaction every couple of minutes, perpetuating the cycle of DNA denaturing and synthesis. This process, generates exponential exact copy of the original template DNA sequence.

PCR cycles
PCR Cycle Target Copies
1 2
2 4
3 8
4 16
5 32
6 64
7 128
8 256
9 512
10 1024
15 32,768
20 1,048,578
25 33,554,432
30 1,073,741,842
Polymerase chain reaction (PCR) amplifies DNA specific to genetic sequence of interest, enabling the monitoring and diagnose molecular abnormalities such as single gene disorders using minute samples such as embryonic cells, blood & tissue [41]

fast and inexpensive way of copying a target sequence of DNA
aids the diagnosis of single cell defects
rapid generation of results within a couple hours
can start from a single molecule of DNA, therefore is more sensitive
has a flexible primer design enabling
overcame previous issues associated with the limited availability of sites of end
generates the DNA copies exponentially
enables DNA amplification required for molecular and genetic analysis
Valid diagnostic method in selecting unaffected embryos for embryo transfer [42] [43]
only during this exponential DNA replication phase can we determine the starting quantity sequence contained in the original sample ( template DNA strand)
PCR reaction is limited by the presence of inhibitors present in the sample : reagent inhibitors
self annealing due to the accumulation of the product -stopping exponential amplification for the target sequence and reach a plateau

quantification of the end point of reaction of PCR products unreliable - therefore that is why we require real time quantitative RT-PCR necessary [44]

Fluorescent In Situ Hybridisation (FISH)


Fluorescence in situ hybridization (FISH) the one of the most effective and rapid [45] Preimplantation Genetic Diagnosis (PGD). This techniques used to locate a specific DNA sequences within a chromosome. FISH facilitates the clinical diagnosis of chromosomal abnormalities indicated by sequential duplications, deletions and rearrangements of chromosome, that are usually missed with microscopic analysis. This technique is especially relevant for female embryos with X-linked diseases,[46] that have no other mutation specific tests [20] As part of PGD, samples are collected from various stages of the embyro,and they are able to conducted tests on the blastocyst, a polar body biopsy and the blastomeres [47]. FISH is 99% effective when used in conjunction with competitive Genomic Hybridisation (CGH) to diagnose chromosomal abnormalities[45].


Samples are collected from either the blastocyst, a polar body biopsy or the blastomeres stages of the embryo [48]. DNA strands are heated and denatured causing their the individual DNA strands to break apart Probes are single complimentary stands of DNA a that have been tagged with small chemical agents that glow brightly in the presence of a specific region on a chromosome. These specific probes then hybridize and join to their complementary DNA strand. The fluorescent tags enable the researchers to correctly identify the presence or lack thereof and location of the specific chromosomes that they are testing for. [49] Researcher analyse the results by identifying the number and the relative location of the fluorescent dots generated by the FISH images.[50] The probe will not fully hybridise if there has been a duplication or a deletion of the DNA - indicating chromosomal and sex chromosomal anomalies like trisomies and aneuploidies. [51]

Different probes are used for different purposes: [52]

  • Locus specific tags detect very small imbalances, and locate isolated small portions

of genes within a chromosome

  • Alphoid/Centomeric Repeat probes are developed from the repetitive sequence located in the middle region of each chromosome, useful in determining the number of chromosomes , detecting rearrangement and when used in conjunction with locus probes to determine the absence of genetic material on a chromosome.
  • Paint Probes are collections of smaller probes with their own stains that bind to a different section on the chromosome - allowing the full chromosome too be labeled a unique colour, this "full colour map" can be used to know the spectral karyotype- full chromosomal mapping is useful in examining chromosomal abnormalities.
FISH We are able to tag Specific DNA sequences using Probes which have been tagged with fluorescent Labels.This technique enables the clinical diagnosis of chromosomal abnormalities, indicated by sequential duplication, deletions and rearrangements of chromosome [53]
FISH is 99% effective when used in conjunction with Competitive Genomic Hybridisation (CGH) to diagnose chromosomal abnormalities.[54]
Rapid generation of results
Identifies very small translocations and aneuploidies that occur within chromosomes, that would usually be missed under microscopic analysis
Indicates whether the accessed chromosomes are normal [55]
Tests for the most common chromosomal abnormalities - down syndrome chromosomes 13,16,18,21 and 22 [56]
It may be used to compare the chromosomal gene arrangements in related species
can be used to identify and remove inheritable X-linked disease or sex chromasome anomalies such as Duchennes Muscular Dystrophy, hemophilia, ectodermal dysplasia [57]
FISH destroys all cells tested [58]
It does not fully access all chromosomes (only ~ 12)
Analysis of results is dependent upon the dot quality impacted by hybridisation efficiency or the camera sensitivity [59]
some studies indicate that using FISH on a day-3 embryo biopsy decreases the rate of live births [60]

Array Comparative Genomic Hybridisation (aCGH)


aCGH also known as Microarray analysis efficiently scans the entire genome for chromosomal imbalances. CGH was initially developed to detect the number of changes in a solid tumor mass. It uses 2 genomes comparing the sample to the control, with each labeled in a different fluorescent dye[61]. Earlier CGH techniques were limited by the resolution of the imaging [62] , these initial limitations were overcome by using Microarrays in conjunction with CGh to improve the resolution of the imaging, Array Comparative Genomic Hybridisation (aCGH). This method compares sample and control microarrayed slides containing small segments of DNA (probes). [63] the Probes used will vary according from the small (25-85 base pairs) oligonucleotides manufactured to highlight different target sequences, to the very large genomic clones (80,000- 200,00 base pairs), and as these are significantly smaller than the traditional metaphase chromosomes used for CGH, generating a higher resolution of image. [64].aCGH is used as a diagnostic tool for prenatal detection f chromosomal abnormalities [65].


[66] The sample is obtained (skin, blood or fetal cells) and DNA is obtained. As a part of PGD fetal cell samples are collected from; the fertilized egg polar bodies, the blastomere (day 3 embryo) or the blastocyst/tropoectoderm stage (day 5 embryo). Sample DNA is labeled with one fluorescent dye, and the control DNA is labeled with a different colored fluorescent dye. the control DNA is used as the base point of reference. heated and denatured single DNA strands then hybridize to their complementary single strand probes, which are then combined and applied to a microarray and the results are run through a computer program and a digital imaging system is used to quantify the results( fluorescent intensities of the labeled probes).

aCGH checks the entire genome for chromosomal imbalances, by comparing control and a sample slides contatining small segements of DNA sample microarrayed slides small segments of DNA. Illustrated by student z5020317 and adapted from [67] [68]

The fluorescent ratio and the hybridization signal at different locations on the genome of the control DNA are used to identify any variances present in the sample DNA. aCGH facilitates the clinical diagnosis of submicroscopic chromosomal duplication, deletion and rearrangements indicative of chromosomal disorders such as trisomies 1-22and specific sex linked disorders. Duplications in the DNA are displayed by the computer program as spikes/ peaks over an established threshold and deletions in DNA are displayed by the computer program as spikes/ toughs beneath this threshold

Advantages Disadvantages
multiple applications: prenatal genetic diagnosis, cancer diagnosis, [69] genetic screening for developmental delay (learning disabilities) [70]. or congenital anomalies that are suspected to be genetic in origin [71] translocations and inversions of DNA are not detected
trace represents all chromosomes present in the human genome chromosomes 1-22 and the X & Y chromosomes, and therefore is the most accurate method for testing whole embryo aneuploidy limited ability diagnosing specific polyploidies such as triploidy [72]
aCGH has been extensively tested, and Validated, and is now used world wide. will not detect mosaicism detection <20% (cultures where >1 of 5 cells are trisomy 12)
detects deletions and additions and rearrangements as well as amplification, of the WHOLE genome, simultaneously. will not detect balanced chromosomal rearrangement
detects submicroscopic alterations will not detect duplications or deletions <80kb
used as a diagnostic tool for prenatal detection of chromosomal abnormalities [73] will not detect point mutations within genes [74]
provides high resolution genomewide screening of segmental genomic copy number variations will not detect chromosomal position of genomic gains
very accurate when used in conjunction with FISH will not detect loos of heterozygosity (LOH) or Absence of heterozygosity (AOH) [75]
Alone is more reliable and in detecting chromosomal abnormalities, with a higher implantation success rate, than FISH [76]
Allows an in depth research focus upon specific types of rearrangements within selected chromosomal regions, a recent particular area of interest is subtelomeric and pericentromeric rearrangements
reduces the risk of failed implantation and miscarriage, improving the chance of a healthy baby [77]

Next Generation Sequencing


The development and advances within ART in the past 20 years, as well as the increasing popularity of IV, has lead to an influx of new technologies developed to screen embryos for chromosomal anomalies, which are covered by the umbrella term of Next generation Sequencing (NGS). NGS is a general term used to describe all of the new and emerging screening techniques currently being introduced and used as part of PGD for IVF . NGS screens for single gene disorders as well as conducting extensive and very comprehensive chromosome diagnosis by sequencing, counting, and accurately assembling millions of DNA reads, simultaneously. [78] There is a movementfor NGS to replace the other limited testing techniques and be used as the standard.


Samples are collected from either blastomere or the blastocyst/tropoectoderm and processed for analysis by a computer system. The methodology of each process is unique to the technique being used.

Advantages Disadvantages
cheaper there are limited information available to clinical applications of NGS [79]
opens new diagnostic possibilities
accurately tests all 24 chromosomes
tests for the presence of monogenic diseases of known genetic background
reduces the number of biopsies required for diagnosis
higher detection rate of small translocations
highly accurate is testing for compound point mutations, chromosomal duplication, deletions and insertions [80]
it accurately detects chromosomal aneuploidy and unbalanced rearrangement [81]
NGS single gene disorder screenings can conducted in conjunction with PCR comprehensive chromosomal screening
Reduces human error
better detects the presence of mosaicism
work well in conjunction with CGH and aCGH as part of PGD, improving the chances of IVF. [82]


There are a large amount of diseases that PGD can apply to, below are descriptions of the diseases that PGD are more commonly used for.

Cystic Fibrosis

Cystic fibrosis is a single gene disorder. It is autosomal recessive and involves mutations in the cystic fibrosis transmembrane conductance regulator (CTFR) gene. The CTFR gene is normally responsible for the decrease in chloride and the transport of bicarbonate in epithelial cells thus playing a major physiological role. In PGD procedures, identification of the gene is assisted by microsatellite markers that have similar composition to the CTFR gene itself. Biopsy of two cells at the blastocyst stage is recommended if markers are not available. There are many variations of cystic fibrosis the most common being P.Phe508del [83].

Duchenne Muscular Dystrophy

Duchenne Muscular Dystrophy is an X-linked recessive disease. It involves the Xp21 gene where majority of the mutations are chromosomal deletions with a smaller percentage resulting from duplications [84].

β – Thalassemia

β – Thalassemia is known as the most common type of autosomal recessive inherited disorder among haemoglobinopathies. It involves the adult β-globin gene and is associated with the absent or decreased expression of the gene. This is commonly caused by a single nucleotide change in the gene. PGD has been used successfully worldwide to identify the β-globin gene where its application is usually performed on a single blastomere or polar body [85].

Applicable diseases for PGD [86], [87], [88]
Disease Involved Genes
5 Alpha Reductase Deficiency (5ARD) SRD5A2
Achondroplasia FGFR3
Acute Intermittent Porphyria ALAD, ALAS2, CPOX, FECH, HMBS, PPOX, UROD, or UROS
Adrenoleukodystrophy (Adrenomyeloneuropathy) ABCD1
Agammaglobulinaemia (x-linked) BTK
Agammaglobulinemia Bruton Tyrosine Kinase (BTK) BTK
Aicardi Goutieres Syndrome 1 (AGS1) TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1
Alagille Syndrome JAG1 or NOTCH2
Alpers-Huttenlocher Syndrome POLG
Alpha-1-antitrypsin deficiency SERPINA1
Alpha-Mannosidosis MAN2B1
Alpha Thalassemia HBA1 or HBA2
Alports Syndrome COL4A3, COL4A4, COL4A5
Alzheimer's Disease - early onset (Type 3 and 4) APP, PSEN1, or PSEN2
Amyotrophic Lateral Sclerosis 1 (ALS1) C9orf72, SOD1, TARDBP, FUS, ANG, ALS2, SETX, VAPB
Argininosuccinic Aciduria ASL
Arrhythmogenic Right Ventricular Cardiomyopathy/ Dysplasia (ARVC/D) DSG2; DSP; PKP2
Ataxia Telangiectasia ATM
Bardet-Biedl Syndrome (BBS) BBS1; BBS10
Barth Syndrome TAZ
Beta Thalassaemia HBB
Birt-Hogg-Dubé Syndrome FLCN
Breast Ovarian Cancer Familial Susceptibility (BRCA2) BRCA1; BRCA2
Canavan Disease ASPA
Carnitine-Acylcarnitine Translocase Deficiency SLC25A20
Cerebral Arteriopathy with Subcortical Infarcts & Leukoencephalopathy (CADASIL) NOTCH3
Cerebral Cavernous Malformation CCM1
Charcot-Marie-Tooth Disease GJB1; MPZ; NEFL; PMP22
CHARGE Syndrome CHD7
Cherubism SH3BP2
Choroideremia CHM
Chronic Granulomatous Disease CYBB; NCF1
Ciliary Dyskinesia DNAH5
Citrullinemia ASS1
Cleidocranial Dysplasia RUNX2
Cockayne Syndrome ERCC6
Congenital Adrenal Hyperplasia CYP21A2
Congenital Cataracts GJA8; VSX2
Congenital Diarrhea, Syndromic SPINT2
Congenital Disorders of Glycosylation (CDG) ALG1; ALG6; CDG1C; DOLK; PMM2
Cornelia de Lange Syndrome NIPBL
Craniosynostosis TWIST1
Crouzon Syndrome FGFR2
Cysteinyl Leukotriene Receptor 1 Deficiency CYSLTR1
Cystic Fibrosis CFTR
Diamond –Blackfan Anemia RPS19
Duchenne Muscular Dystrophy DMD
Dyskeratosis congenita (Male embryos only) DKC1
Ectodermal dysplasia (Hypohidrotic) EDA; EDA1; GJB6; IKBKG
Familial Adenomatous polyposis coli (FAP) APC
Familial Dysautonomia IKBKAP
Fragile X Syndrome (FRAX) FMR1
Galactosemia GALT
Gangliosidosis GLB1
Glanzmann Thrombasthenia ITGA2B
Glutaric Acidemia (aciduria) GCDH
Glycogen Storage Disease G6PC; GAA; SLC37A4
Haemophilia A F8
Haemophilia B F9
Hereditary Nonpolyposis Colorectal Cancer: Lynch Syndrome MLH1; MSH2; MSH6
Holt Oram Syndrome TBX5
Huntington Disease HD
Hydrocephalus L1CAM
Ichthyosis ABCA12; STS
Incontinentia Pigmenti (IP) NEMO
Joubert Syndrome 5 INPP5E
Krabbe Disease GALC
Leber Congenital Amaurosis (LCA) CEP290; GUCY2D
Leigh Syndrome (Infantile Subacute Necrotising Encephalopathy) LRPPRC
Lesch Nyan Syndrome HPRT1
Leukocyte Adhesion Deficiency (Type I) ITGB2
Li-Fraumeni Syndrome TP53
Macular Dystrophy Retinal VMD2
Maple Syrup Urine Disorder (MSUD) BCKDHB
Marfan Syndrome FBN1
Menkes Syndrome ATP7A
Mitochondrial DNA Depletion Syndrom POLG; RRM2B; SUCLA2; TK2
Mucolipidosis type II GNPTAB
Multiple Endocrine Neoplasia MEN1; MEN2A; MEN2B
Multiple Exostoses EXT1; EXT2
Myotubular myopathy MTM1
Nail-Patella Syndrome LMX1B
Neurofibromatosis Type 1 NF1
Neurofibromatosis Type 2 NF2
Noonan Syndrome KRAS, PTPN11; SOS1
Norrie Disease NDP
Ocular Albinism GPR143
Oculocutaneous Albinism OCA2; TYR
Oculodentaldigital Dysplasia GJA1
Optic Atrophy OPA1
Ornithine Transcarbamylase Deficiency OTC
Osteogenesis imperfeca COL1A1; COL1A2
Osteopetrosis CLCN7; OSTM1; TCIRG1
Pachyonychia Congenita KRT16; KRT6A
Pancreatitis, Hereditary PRSS1
Papillorenal syndrome PAX2
Phenylketonuria PAH
This table does not cover the complete list of diseases that PGD can be applied to.

Laws & Legal status


PGD is currently used to detect serious genetic conditions to improve the outcome of Assisted Reproductive Technologies (ART). In very rare cases it may be used to select an embryo with compatible tissue for a sibling who has a life-threatening disease where other means of treatment is unavailable. This is with the conditions that the use of PGD will not affect the welfare and interests of the child to be born. The parents must also receive adequate counselling and have full understanding of the procedures of PGD. [89] The use of PGD for sex-selection is prohibited with the exception of reducing the risk of the transmission of serious sex-linked genetic conditions. [89]


The laws regarding PGD in Brazil are not strictly regulated. They are vague and there is limited information surround the activities of assisted reproduction in general in the country [90].

Czech Republic

The laws in the Czech Republic allow those with a “defined indication in order to exclude risk of serous genetically conditioned disease and defects with embryos before they are implanted into the cavity of the uterus”. Couples that undergo any assisted reproductive treatment including PGD have to be married. Sex-selection is illegal except in regards to serious sex-linked genetic diseases [91].


In Greece, ART is open to those up to the age of 50 with written consent. It can only be used if a medical necessity is present such as the susceptibility of serious hereditary diseases. Sex selection is banned apart from cases of sex-linked diseases and sexually transmitted diseases [91].


ART is only available to those who are married or have a similar type of relationship for at least two years. The couples cannot be of the same sex and must be at least 18 years of age. Sex selection is illegal except in cases of sex-linked diseases. The use of PGD is illegal if the predictive value of genetic tests are very low [91].


PGD can be applied to “serious hereditary diseases not amenable to postnatal curative treatment” and “detection of other abnormalities which may compromise the viability of the pre-embryo”. If PGD is to be used for any other purpose authorisation must be acquired [91].


The use of PGD is strictly regulated and couples must achieve authorisation of the National Board of Health and Welfare. It can only be used it can only be used if the child is at risk to inheriting a serious chromosomal or monogenetic disease. It cannot be used for selection of specific characteristics [91].

United Kingdom

Those involved with carrying out the IVF treatment must have a license from the Human Fertilisation and Embryology Authority (HFEA). Only embryos that are approved by the HFEA can be implanted where the embryonic nuclear or mitochondrial DNA cannot be altered with the exception of preventing mitochondrial diseases [91].

Future/Current Research

Noninvasive Preimplantation Genetic Testing without Embryo Biopsy

Different parameters of gametes, zygotes, embryos (“vacuoles in sperm heads, spindle position in mature oocytes, cleavage intervals of zygote, and embryo developmental dynamics”) may correlate with aneuploidy rates. This knowledge may be applied in potential noninvasive preimplantation diagnostic methods. Several methods have been proposed and are currently further researched[34].

Sperm Selection

Intracytoplasmic morphologically selected sperm injection (IMSI) is common procedure in IVF treatment to improve fertilization rates in patients with poor semen quality. In addition, studies have found that IMSI improves embryo development and that spermatozoa with large vacuoles in their heads correlate with increased aneuploidy rates and disturbed chromosomal structures. Thus, selecting spermatozoa based on morphological hallmarks may decrease aneuploidy rates in the fertilized embryos. As with polar body biopsies, however, this approach will solely be applicable if evidence for severe male detrimental contribution is given[34].

Blastocoel Fluid Extraction

In addition, a less invasive retrieval of material for diagnosis could include the extraction of the blastocoel fluid. The cavity of the blastocyst, lined by the trophectoderm, is filled with this blastocoel fluid, which contains metabolites of both trophectoderm and inner cell mass origin. The retrieval does not require a biopsy but merely a small opening to extract the fluid and, thus, causes less harm to the embryo. Multiple studies have applied this method[92] [93] and it may in the future become of clinical relevance.

Aspiration of the Blastocoel Fluid using a ICSI pipette[34].

Next to metabolites, the blastocoel fluid can contain DNA. Studies have shown that genomic DNA is present in about 90% of the blastocoel fluid samples tested. Typically the fluid is removed with an ICSI pipette from a day five blastocyst through its mural trophectoderm until the blastocyst fully collapses around the embryo. Several concerns regarding this method in a clinical setting have been raised. The collected DNA may be contaminated by the culture media that contains DNA fractions. The DNA may also be least representative of the actual embryos genome as the DNA may originate from abnormal or degenerated cells. Even though labelled noninvasive, the blastocyst still undergoes manipulation to some degree which may affect its viability. Thus, more research is required until this method can evolve from research to clinical use[34].


The protein secretome of blastocysts may be representative of its chromosome constitution Recent studies have found biomarkers such as lipocalin-1, interleukin-10, tumor necrosis factor, stem cell factor, and chemokine ligand 13 to be differently secreted by aneuploid blastocyst than by euploid ones. The most significant biomarker appears to be interleukin-10. Paired with novel proteomic technologies and mass spectrometry this knowledge when extended may contribute to a new invasive preimplantation genetic diagnosis method[34].

Embryo Morphology

Using time lapse imaging the embryo’s morphology can be closely observed and potential aneuploidy characteristics detected. Such characteristics may include the time of division to five cells, the time between the division from three to four cells, and the duration of the division from one to two and subsequently to three. In addition, the morphological quality of ICM an TE has been positively associated with aneuploidy or euploidy prognosis[94]. These may give rise to an embryo quality screening prior to implantation[34].

Utilization of Diseased Cell Lines



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