2024
Chromosome Division in Early Embryos-Is Everything under Control? And Is the Cell Size Important?
HORÁKOVÁ, Adéla, Markéta KONEČNÁ a Martin ANGERZákladní údaje
Originální název
Chromosome Division in Early Embryos-Is Everything under Control? And Is the Cell Size Important?
Autoři
HORÁKOVÁ, Adéla (203 Česká republika, domácí), Markéta KONEČNÁ (203 Česká republika, domácí) a Martin ANGER (203 Česká republika)
Vydání
International Journal of Molecular Sciences, MDPI, 2024, 1661-6596
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10605 Developmental biology
Stát vydavatele
Švýcarsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 5.600 v roce 2022
Organizační jednotka
Přírodovědecká fakulta
UT WoS
001172049100001
Klíčová slova anglicky
spindle; chromosome division; segregation errors; spindle assembly checkpoint; embryo; CDK1; cell size; aneuploidy
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 25. 3. 2024 09:40, Mgr. Marie Šípková, DiS.
Anotace
V originále
Chromosome segregation in female germ cells and early embryonic blastomeres is known to be highly prone to errors. The resulting aneuploidy is therefore the most frequent cause of termination of early development and embryo loss in mammals. And in specific cases, when the aneuploidy is actually compatible with embryonic and fetal development, it leads to severe developmental disorders. The main surveillance mechanism, which is essential for the fidelity of chromosome segregation, is the Spindle Assembly Checkpoint (SAC). And although all eukaryotic cells carry genes required for SAC, it is not clear whether this pathway is active in all cell types, including blastomeres of early embryos. In this review, we will summarize and discuss the recent progress in our understanding of the mechanisms controlling chromosome segregation and how they might work in embryos and mammalian embryos in particular. Our conclusion from the current literature is that the early mammalian embryos show limited capabilities to react to chromosome segregation defects, which might, at least partially, explain the widespread problem of aneuploidy during the early development in mammals.