TY - JOUR
T1 - It's about time
T2 - Ossification center formation in C57BL/6 mice from E12-E16
AU - Flaherty, Kevin
AU - Richtsmeier, Joan T.
N1 - Funding Information:
Funding: This research was funded by NIH/NIDCR R01 DE022988, NIH/NICHD P01 HD078233, NIH/NIDCR R01 DE027677, NSF BCS-1650824 and a collaborative research travel grant from the Burroughs Wellcome Fund (2013).
Publisher Copyright:
© 2018 by the authors.
PY - 2018/12/1
Y1 - 2018/12/1
N2 - The establishment of precise, high-resolution temporal sequences for morphogenetic events in laboratory mice remains a vexing issue in developmental biology. Mouse embryos collected at the same period of gestation, even those from the same litter, show wide variation in individual levels of progress along their developmental trajectory. Therefore, age at harvest does not provide sufficient information about developmental progress to serve as the basis for forming samples for the study of rapidly or near-simultaneously occurring events such as the sequence of ossification center formation. Here, we generate two measures of individual developmental progress (developmental age) for a large sample of mouse embryos using crown-rump lengths that measures size, and limbstaging ages produced by the embryonic Mouse Ontogenetic Staging System (eMOSS) that measure shape. Using these measures, we establish fine-grained sequences of ossification center appearance for mouse embryos. The two measures of developmental progress generate slightly different sequences of ossification center formation demonstrating that despite their tight correlation throughout the developmental period, size and shape are aspects of form that are at least partially dissociated in development.
AB - The establishment of precise, high-resolution temporal sequences for morphogenetic events in laboratory mice remains a vexing issue in developmental biology. Mouse embryos collected at the same period of gestation, even those from the same litter, show wide variation in individual levels of progress along their developmental trajectory. Therefore, age at harvest does not provide sufficient information about developmental progress to serve as the basis for forming samples for the study of rapidly or near-simultaneously occurring events such as the sequence of ossification center formation. Here, we generate two measures of individual developmental progress (developmental age) for a large sample of mouse embryos using crown-rump lengths that measures size, and limbstaging ages produced by the embryonic Mouse Ontogenetic Staging System (eMOSS) that measure shape. Using these measures, we establish fine-grained sequences of ossification center appearance for mouse embryos. The two measures of developmental progress generate slightly different sequences of ossification center formation demonstrating that despite their tight correlation throughout the developmental period, size and shape are aspects of form that are at least partially dissociated in development.
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U2 - 10.3390/jdb6040031
DO - 10.3390/jdb6040031
M3 - Article
C2 - 30558321
AN - SCOPUS:85059244712
SN - 2221-3759
VL - 6
JO - Journal of Developmental Biology
JF - Journal of Developmental Biology
IS - 4
M1 - 31
ER -