Difference between revisions of "BGDA Practical 3 - Gametogenesis"

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| Trisomy 21 female karyotype
 
| Trisomy 21 female karyotype
 
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* Autosomal chromosome aneuploidy
 
* Autosomal chromosome aneuploidy
 
** '''trisomy 21''' - [[trisomy 21|Down syndrome]]
 
** '''trisomy 21''' - [[trisomy 21|Down syndrome]]
 
** '''trisomy 18''' - [[trisomy 18|Edwards syndrome]]
 
** '''trisomy 18''' - [[trisomy 18|Edwards syndrome]]
 
** '''trisomy 13''' - [[Trisomy_13|Patau syndrome]]
 
** '''trisomy 13''' - [[Trisomy_13|Patau syndrome]]
 
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* Sex chromosome aneuploidy
 
* Sex chromosome aneuploidy
 
** monosomy X - Turner's Syndrome
 
** monosomy X - Turner's Syndrome
 
** trisomy X - [[Trisomy_X|Triple-X syndrome]]
 
** trisomy X - [[Trisomy_X|Triple-X syndrome]]
 
** 47 XXY - Klinefelter's Syndrome
 
** 47 XXY - Klinefelter's Syndrome
 
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== Male Gametogenesis ==
 
== Male Gametogenesis ==
 
[[File:Seminiferous-tubule-HEx40.jpg|thumb|Adult seminiferous tubule showing spermatozoa developmental stages]]
 
[[File:Seminiferous-tubule-HEx40.jpg|thumb|Adult seminiferous tubule showing spermatozoa developmental stages]]

Revision as of 14:01, 16 May 2014

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Practical 3: Oogenesis and Ovulation | Gametogenesis | Fertilization | Early Cell Division | Week 1 | Implantation | Week 2 | Extraembryonic Spaces | Gastrulation | Notochord | Week 3

Female Gametogenesis

Oocyte and support cells in an astral follicle

In females, the total number of eggs ever to be produced are present in the newborn female.

  1. All eggs are arrested at an early stage of the first meiotic division as a primary oocyte (primordial follicle). Following purberty, during each menstrual cycle, pituitary gonadotrophin stimulates completion of meiosis 1 the day before ovulation.
  2. In meiosis 1, a diploid cell becomes 2 haploid (23 chromosomes) daughter cells, each chromosome has two chromatids. One cell becomes the secondary oocyte the other cell forms the first polar body.
  3. The secondary oocyte then commences meiosis 2 which arrests at metaphase and will not continue without fertilization.
  4. At fertilization meiosis 2 completes, forming a second polar body. Note that the first polar body may also undergo this process forming a third polar body.

Female gametogenesis

Female Abnormalities

Meiotic non-disjunction resulting in aneuploidy, most are embryonic lethal and not seen. The most common non-lethal abnormality is Trisomy 21 or Down syndrome. The potential for this and most genetic abnormalities increase with maternal age.

Trisomy21female.jpg Turner syndrome karyotype.jpg
Trisomy 21 female karyotype Turner's Syndrome karyotype
  • Sex chromosome aneuploidy
    • monosomy X - Turner's Syndrome
    • trisomy X - Triple-X syndrome
    • 47 XXY - Klinefelter's Syndrome

Male Gametogenesis

Adult seminiferous tubule showing spermatozoa developmental stages

The histology will be covered in a separate [http://vslides.unsw.edu.au/VirtualSlideV2.nsf/wFrameset?OpenFrameSet&Frame=NotesView&Src=%2FVirtualSlideV2.nsf%2Fid%2F37AFC0%3FOpenDocument%26AutoFramed

Male Histology Practical] (support page).

In males, sperm continues to be generated throughout life from a stem cell population in the testis. Spermatozoa maturation involves two processes meiosis and spermiogenesis Male gametogenesis.jpg

The above figure compares meiosis to the female (the polar bodies have been removed and labelling updated).

Human Spermatozoa Development

  • Spermatogenesis process of spermatagonia mature into spermatazoa (sperm).
  • Continuously throughout life occurs in the seminiferous tubules in the male gonad- testis (plural testes).
  • At puberty spermatagonia activate and proliferate (mitosis).
  • about 48 days from entering meiosis until morphologically mature spermatozoa
  • about 64 days to complete spermatogenesis, depending reproduction time of spermatogonia
  • follicle stimulating hormone (FSH) - stimulates the spermatogenic epithelium
  • luteinizing-hormone (LH) - stimulates testosterone production by Leydig cells

Spermiogenesis

Human spermatozoa acrosomal protein SP-10.jpg

Human-spermatozoa EM01.jpg

Spermatozoa animation icon.jpg Mature human spermatozoa
  • 60 µm long, actively motile
  • divided into 3 main regions (head, neck and tail)
  • head - (flattened, 5 µm long by 3 µm wide) the nucleus and acrosome. Posterior part of nuclear membrane forms the basal plate.
  • neck - (1 µm) attached to basal plate, transverse oriented centriole, contains nine segmented columns of fibrous material, continue as outer dense fibres in tail.
  • tail - 3 parts a middle piece, principal piece and end piece
    • middle piece - (5 µm long) axonema and dense fibres surrounded by mitochondria
    • principal piece - (45 µm long) fibrous sheath interconnected by regularly spaced circumferential hoops
    • end piece - (5 µm long) axonema surrounded by small amount of cytoplasm and plasma membrane


Links: Spermatozoa Development | MBoC - Sperm | MBoC - Highly simplified drawing of a cross-section of a seminiferous tubule in a mammalian testis | MBoC - Cytoplasmic bridges in developing sperm cells and their precursors

Puberty

  • In humans at puberty, hormonal and morphological changes occur within the gonad and other systems (secondary sex characteristics).
  • Within the testis the immature Sertoli cells cease to proliferate and differentiate.
  • Spermatogonium (plural, spermatogonia) proliferate and spermatogenesis begins.
  • It takes about 70 days for cells to mature from the diploid spermatogonium to a primary spermatocyte.
  • This maturation occurs in waves along the seminiferous tubules.

Ejeculate

Azoospermia - Non-obstructive azoospermia (NOA) and Obstructive azoospermia (OA)
  • release of spermatozoa and accessory gland secretions from the male genital tract (3.5 ml)
  • 200-600 million sperm, by volume less than 10 % spermatozoa
  • Accessory Gland secretions - 60 % seminal vesicle, 30 % prostate and 10 % bulbourethral

Male Abnormalities

  • Oligospermia - (Low Sperm Count) less than 20 million sperm after 72 hour abstinence from sex
  • Azoospermia - (Absent Sperm) blockage of duct network
  • Immotile Cilia Syndrome - lack of sperm motility

Differences in Mammalian Meioses

Female Oogenesis Male Spermatogenesis
Meiosis initiated once in a finite population of cells continuously in mitotically dividing stem cell population
Gametes produced 1 / meiosis 4 / meiosis
Meiosis completed delayed for months or years completed in days or weeks
Meiosis Arrest arrest at 1st meiotic prophase no arrest differentiation proceed continuously
Chromosome Equivalence All chromosomes exhibit equivalent transcription and recombination during meiotic prophase Sex chromosomes excluded from recombination and transcription during first meiotic prophase
Gamete Differentiation occurs while diploid (in first meiotic prophase) occurs while haploid (after meiosis ends)



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Practical 3: Oogenesis and Ovulation | Gametogenesis | Fertilization | Early Cell Division | Week 1 | Implantation | Week 2 | Extraembryonic Spaces | Gastrulation | Notochord | Week 3


Additional Information

Additional Information - Content shown under this heading is not part of the material covered in this class. It is provided for those students who would like to know about some concepts or current research in topics related to the current class page.
Chromosome structure

The information below is not part of today's Practical.

  • Male Histology - covered in a later practical class.
  • Genetic Information - covered elsewhere in your course.
  • Cell Biology - Mitosis and meiosis covered in Foundations.

Male Histology

This will be covered in detail in a separate Histology practical class. Virtual Slides

From today's class you should have a basic understanding of seminiferous tubule structure in relation to spermatozoa development.

Genetics

Where genes are located and how they are inherited relate to the chromosome that the gene is located upon, the parental origin of the gene and the dominant/recessive nature of the gene.

Inheritance Pattern images: Genetic Abnormalities | autosomal dominant | autosomal recessive | X-linked dominant (affected father) | X-Linked dominant (affected mother) | X-Linked recessive (affected father) | X-Linked recessive (carrier mother) | mitochondrial inheritance | Codominant inheritance | Genogram symbols | Genetics

Mitosis and Meiosis

Mitosis and meiosis.jpg


Links: Mitosis | Meiosis

Terms

  • autosomal inheritance - some hereditary diseases are described as autosomal which means that the disease is due to a DNA error in one of the 22 pairs that are not sex chromosomes. Both boys and girls can then inherit this error. If the error is in a sex chromosome, the inheritance is said to be sex-linked.
  • cascade testing - Clinical genetic term for the testing of genetic relatives for a mutation that has been identified in the first affected family member. Abnormal Development - Genetic
  • gene - a sequence of DNA that encodes an individual protein.
  • genome - the complete genetic information in the form of DNA available to a specific species.
  • sperm - See spermatozoa. The male haploid reproductive cell, often used generically (and incorrectly) to describe these cells and the fluid of the ejaculate. Term is a shortened form of scientifically correct term spermatazoa.
  • sperm annulus - (Jensen's ring; Latin, annulus = ring) A region of the mammalian sperm flagellum connecting the midpiece and the principal piece. The annulus is a septin-based structure formed from SEPT1, 4, 6, 7 and 12. Septins are polymerizing GTPases that can act as a scaffold forming hetero-oligomeric filaments required for cytokinesis and other cell cycle roles.
  • spermatid - Intermediate cell in spermatozoa development, within the testis seminiferous tubule they lie in the luminal cell layer to the secondary spermatocyte. These small cells are haploid and in spermiogenesis change their cellular structure and shape to form spermatozoa.
(More? Spermatozoa Development | Testis Development | Fertilization | Lecture - Fertilization)
  • spermatogenesis - (Greek, genesis = origin, creation, generation) The term used to describe the process of diploid spermatagonia division and differentiation to form haploid spermatazoa within the testis (male gonad). The process includes the following cellular changes: meiosis, reoorganization of DNA, reduction in DNA content, reorganization of cellular organelles, morphological changes (cell shape). The final process of change in cell shape is also called spermiogenesis.
  • spermiogenesis - (Greek, genesis = origin, creation, generation) The maturation process of the already haploid spermatids into the mature spermatozoa shape and organization. This process involves reorganization of cellular organelles (endoplasmic reticulum, Golgi apparatus, mitochondria), cytoskeletal changes (microtubule organization) and morphological changes (cell shape, acrosome and tail formation). The process of maturation of the spermatids into spermatozoa: chromatin condenses, nucleus becomes smaller, the Golgi apparatus is modified to form the acrosome, microtubules are reorganised to form the tail, mitochondria are relocated to the initial segment of the tail and the majority of cell cytoplasm is discarded.
  • spermatogonia - These cells form in the embryo from the primordial germ cell and are located in the seminiferous tubule adjacent to the basal membrane. The cells can either divide and separate to renew the stem cell population, or they divide and stay together as a pair (Apr spermatogonia) connected by an intercellular cytoplasmic bridge to begin to differentiate and eventually form spermatazoa.
  • spermatozoa - (spermatozoon, singular term) The male haploid gamete cell produced by meiosis in the testis (male gonad) seminiferous tubule. In humans, produced from puberty onwards and develop from the diploid stem cell the spermatogonia. The developmental meiosis is called spermatogenesis and the final morphologiccal (shape) change is called spermeiogenesis. The mature human spermatozoon formed from the spermatid has a head, neck and tail and is about 60 µm long. At ejaculation these cells undergo capacitation are activated and become motile.
  • spermatozoa head - Following spermiogenesis, the first region of the spermatozoa containing the haploid nucleus and acrosome. In humans, it is a flattened structure (5 µm long by 3 µm wide) with the posterior part of nuclear membrane forming the basal plate region. The human spermatozoa is about 60 µm long, actively motile and divided into 3 main regions (head, neck and tail).
  • spermatozoa neck - Following spermiogenesis, the second region of the spermatozoa attached to basal plate, transverse oriented centriole, contains nine segmented columns of fibrous material, continue as outer dense fibres in tail. In humans, it forms a short structure (1 µm). The human spermatozoa is about 60 µm long, actively motile and divided into 3 main regions (head, neck and tail).
  • spermatozoa tail - Following spermiogenesis, the third region of the spermatozoa that has a (head, neck and tail). The tail is also divided into 3 structural regions a middle piece, a principal piece and an end piece. In humans: the middle piece (5 µm long) is formed by axonema and dense fibres surrounded by mitochondria; the principal piece (45 µm long) fibrous sheath interconnected by regularly spaced circumferential hoops; the final end piece (5 µm long) has an axonema surrounded by small amount of cytoplasm and plasma membrane.
  • spermatogonial stem cells - (SSCs) The spermatagonia cells located beside the seminiferous tubule basal membrane that either divide and separate to renew the stem cell population, or they divide and stay together as a pair (Apr spermatogonia) connected by an intercellular cytoplasmic bridge to differentiate and eventually form spermatazoa.
  • sperm protein 56 - A component of the spermatozoa acrosomal matrix released to the sperm surface during capacitation.



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Practical 3: Oogenesis and Ovulation | Gametogenesis | Fertilization | Early Cell Division | Week 1 | Implantation | Week 2 | Extraembryonic Spaces | Gastrulation | Notochord | Week 3



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Cite this page: Hill, M.A. (2021, August 2) Embryology BGDA Practical 3 - Gametogenesis. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/BGDA_Practical_3_-_Gametogenesis

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© Dr Mark Hill 2021, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G