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Open AccessJournal ArticleDOI

Gastrulation in the mouse: Growth and regionalization of the epiblast

M. H. L. Snow
- 01 Dec 1977 - 
- Vol. 42, Iss: 1, pp 293-303
TLDR
It is calculated that the proliferative zone, in the 24 h period commencing with primitive streak formation, could generate about half the cells in the 7½-day embryo, and it is postulated that the cells generated in the PZ may constitute the ectoderm of later stage embryos.
Abstract
Histological determination of cell numbers in the mouse embryo between 4½ and 7½ days post coitum show that growth during this period, in which gastrulation occurs, is not uniform. Prior to primitive streak formation mean cell generation time is about 9 h. Co-incidental with the appearance of the primitive streak the embryo enters a period of rapid growth, lasting about 24 h, during which the mean cell generation time must be about 5 h in order to account for the increase in cell numbers. A more detailed study, in which variations in mitotic activity in different regions of the embryo have been analysed, has identified a small region, the so-called ‘proliferative zone’, constituting about 10% of the whole epiblast, in which cell generation time may average as little as 2–3 h over a 24 h period. The cell generation time for other epiblast regions is estimated at about 6·5 h. It is calculated that the proliferative zone, in the 24 h period commencing with primitive streak formation, could generate about half the cells in the 7½-day embryo. The topographical consequences of such a rapidly expanding region in the embryo are discussed in the light of other, circumstantial evidence, and it is postulated that the cells generated in the PZ may constitute the ectoderm of later stage embryos.

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Journal ArticleDOI

Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2

TL;DR: Developmental arrest in Brca2-deficient embryos, their radiation sensitivity, and the association of Brca1 with Rad51 indicate that Brca 2 may be an essential cofactor in the Rad51-dependent DNA repair of double-strand breaks, thereby explaining the tumour-suppressor function of BrCA2.
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ATR disruption leads to chromosomal fragmentation and early embryonic lethality.

TL;DR: Data show that ATR is essential for early embryonic development and must function in processes other than regulation of p53, implying that apoptosis is caused by a loss of genomic integrity.
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A Wnt5a pathway underlies outgrowth of multiple structures in the vertebrate embryo.

TL;DR: The reduced number of proliferating cells in both the progress zone and the primitive streak mesoderm suggests that one function of Wnt5a is to regulate the proliferation of progenitor cells, a pathway common to many structures whose development requires extension from the primary body axis.
Journal ArticleDOI

Clonal analysis of epiblast fate during germ layer formation in the mouse embryo

TL;DR: While individual cells in the epiblast sheet behave independently with respect to their neighbours, morphogenetic movement during germ layer formation is coordinated in the population as a whole and indicates that, despite geometrical differences, topological fate relationships are conserved among these vertebrates.
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