File:Aneuploidy model based on fragmentation.jpg: Difference between revisions
(==Model for the Origin of Human Embryonic Aneuploidy Based on Fragmentation Timing== Proposed model for the origin of human embryonic aneuploidy based on fragmentation timing, fragment resorption and underlying chromosomal abnormalities. Human embryos...) |
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Above text from figure legend and [http://www.nature.com/ncomms/journal/v3/n12/full/ncomms2249.html#supplementary-information Supplementary Movies] refers to the original article supplementary information. | Above text from figure legend and [http://www.nature.com/ncomms/journal/v3/n12/full/ncomms2249.html#supplementary-information Supplementary Movies] refers to the original article supplementary information. | ||
:'''Links:''' [[Abnormal Development - Genetic]] | {{Trisomy 21}} | {{Morula}} | |||
===Reference=== | |||
{{#pmid:23212380}} | |||
====Copyright==== | ====Copyright==== | ||
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Figure 5. Ncomms2249-f5.jpg Original figure cropped panel C and altered in size and labelling. | Figure 5. Ncomms2249-f5.jpg Original figure cropped panel C and altered in size and labelling. | ||
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[[Category:Human]][[Category:Morula]] | [[Category:Human]][[Category:Morula]] | ||
[[Category:Genetic Abnormalities]][[Category:Abnormal Development]][[Category:Trisomy 21]] | [[Category:Genetic Abnormalities]][[Category:Abnormal Development]][[Category:Trisomy 21]] | ||
Latest revision as of 13:44, 1 April 2019
Model for the Origin of Human Embryonic Aneuploidy Based on Fragmentation Timing
Proposed model for the origin of human embryonic aneuploidy based on fragmentation timing, fragment resorption and underlying chromosomal abnormalities. Human embryos with meiotic errors (monosomies and trisomies) and those that appear to be triploid typically exhibit fragmentation at the one-cell stage (Supplementary Movie 5), whereas fragmentation is most often detected at the two-cell stage in embryos with mitotic errors (Supplementary Movie 6). We also demonstrate that missing chromosome(s) are contained within fragments (Supplementary Fig. S9a) termed embryonic micronuclei and for those embryos with mitotic errors, propose that the embryo likely divided before these chromosomes properly aligned on the mitotic spindle. The correlation between the timing of fragmentation and the type of embryonic aneuploidy suggests that the embryo may respond to chromosomal abnormalities and undergoes fragmentation as a survival mechanism. As development proceeds, these fragments either remain or are reabsorbed by the blastomere from which they originated or a neighbouring blastomere to generate the complex human aneuploidies observed (Supplementary Movie 4).
Above text from figure legend and Supplementary Movies refers to the original article supplementary information.
- Links: Abnormal Development - Genetic | Trisomy 21 | morula
Reference
Chavez SL, Loewke KE, Han J, Moussavi F, Colls P, Munne S, Behr B & Reijo Pera RA. (2012). Dynamic blastomere behaviour reflects human embryo ploidy by the four-cell stage. Nat Commun , 3, 1251. PMID: 23212380 DOI.
Copyright
http://creativecommons.org/licenses/by-nc-sa/3.0/
Figure 5. Ncomms2249-f5.jpg Original figure cropped panel C and altered in size and labelling.
Cite this page: Hill, M.A. (2024, April 16) Embryology Aneuploidy model based on fragmentation.jpg. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Aneuploidy_model_based_on_fragmentation.jpg
- © Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G
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