Growth and early postimplantation defects in mice deficient for the bromodomain-containing protein Brd4
| Autor: | Elena Grigorieva, Denise Lynch, Rosa S. P. Beddington, Denis Houzelstein, Simon L. Bullock, Valerie Wilson |
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| Rok vydání: | 2002 |
| Předmět: |
Heterozygote
Oncogene Proteins Fusion Transcription Genetic Molecular Sequence Data Cell Cycle Proteins Biology chemistry.chemical_compound Embryonic and Fetal Development Mice Pregnancy Transcriptional regulation Mammalian Genetic Models with Minimal or Complex Phenotypes Inner cell mass Animals Humans Amino Acid Sequence Molecular Biology Gene Cells Cultured Growth Disorders Regulation of gene expression Mice Knockout Sequence Homology Amino Acid Homozygote Chromosome Mapping Gene Expression Regulation Developmental Nuclear Proteins Cell Biology Exons Null allele Molecular biology Bromodomain Methyl methanesulfonate Mice Inbred C57BL Phenotype chemistry Cell culture Female Chromosomes Human Pair 19 Transcription Factors |
| Zdroj: | Houzelstein, D, Bullock, S L, Lynch, D E, Grigorieva, E F, Wilson, V A & Beddington, R S P 2002, ' Growth and early postimplantation defects in mice deficient for the bromodomain-containing protein Brd4 ', Molecular and Cellular Biology, vol. 22, no. 11, pp. 3794-802 . https://doi.org/10.1128/MCB.22.11.3794-3802.2002 |
| ISSN: | 0270-7306 |
| DOI: | 10.1128/MCB.22.11.3794-3802.2002 |
| Popis: | In a gene trap screen we recovered a mouse mutant line in which an insertion generated a null allele of the Brd4 gene. Brd4 belongs to the Fsh/Brd family, a group of structurally related proteins characterized by the association of two bromodomains and one extraterminal domain. Members of this family include Brd2/Ring3/Fsrg1 in mammals, fs(1)h in Drosophila, and Bdf1 in Saccharomyces cerevisiae. Brd4 heterozygotes display pre- and postnatal growth defects associated with a reduced proliferation rate. These mice also exhibit a variety of anatomical abnormalities: head malformations, absence of subcutaneous fat, cataracts, and abnormal liver cells. In primary cell cultures, heterozygous cells also display reduced proliferation rates and moderate sensitivity to methyl methanesulfonate. Embryos nullizygous for Brd4 die shortly after implantation and are compromised in their ability to maintain an inner cell mass in vitro, suggesting a role in fundamental cellular processes. Finally, sequence comparisons suggest that Brd4 is likely to correspond to the Brd-like element of the mediator of transcriptional regulation isolated by Y. W. Jiang, P. Veschambre, H. Erdjument-Bromage, P. Tempst, J. W. Conaway, R. C. Conaway, and R. D. Kornberg (Proc. Natl. Acad. Sci. USA 95:8538-8543, 1998) and the Brd4 mutant phenotype is discussed in light of this result. Together, our results provide the first genetic evidence for an in vivo role in mammals for a member of the Fsh/Brd family. |
| Databáze: | OpenAIRE |
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