Literature DB >> 521742

Ultrastructural studies of lethal c25H/C25H mouse embryos.

M D Nadijcka, N Hillman, S Gluecksohn-Waelsch.   

Abstract

Mouse embryos which are homozygous for the c25H deletion at the albino locus are developmentally arrested at the 2- to 6-cell cleavage stages. This study reveals that the mutant embryos cease development before they can be distinguished ultrastructurally from their normal litter-mates. After prolonged developmental delay (24--48 h), the nuclei of the mutant embryos become extremely aberrant in shape, whereas other subcellular organelles remain normal and there are no signs of pyknosis. Eventually, the mutant embryos do become pyknotic and begin to degenerate. The striking effects of this deletion on nuclear ultrastructure of cleavage-stage embryos are discussed in relation to biochemical and ultrastructural defects caused by other lethal deletions at the albino locus.

Entities:  

Mesh:

Year:  1979        PMID: 521742

Source DB:  PubMed          Journal:  J Embryol Exp Morphol        ISSN: 0022-0752


  3 in total

1.  The albino-deletion complex of the mouse: molecular mapping of deletion breakpoints that define regions necessary for development of the embryonic and extraembryonic ectoderm.

Authors:  S K Sharan; B Holdener-Kenny; S Ruppert; A Schedl; G Kelsey; E M Rinchik; T Magnuson
Journal:  Genetics       Date:  1991-11       Impact factor: 4.562

2.  Genomic mapping within the albino-deletion complex using individual early postimplantation mouse embryos.

Authors:  S K Sharan; B Holdener-Kenny; D W Threadgill; T Magnuson
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

3.  Development of Dickie's small eye: an early lethal mutation in the house mouse.

Authors:  K Theiler; D S Varnum; L C Stevens
Journal:  Anat Embryol (Berl)       Date:  1980
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.