The RNA binding protein Zfp36l1 is required for normal vascularisation and post-transcriptionally regulates VEGF expressiono

被引:78
作者
Bell, Sarah E.
Sanchez, Maria Jose
Spasic-Boskovic, Olivera
Santalucia, Tomas
Gambardella, Laure
Burton, Graham J.
Murphy, John J.
Norton, John D.
Clark, Andrew R.
Turner, Martin
机构
[1] Babraham Inst, Lab Lymphocyte Signalling & Dev, Cambridge CB2 4AT, England
[2] Univ Cambridge, Dept Haematol, Cambridge Inst Med Res, Cambridge, England
[3] Univ Cambridge, Dept Anat, Cambridge, England
[4] Univ London Imperial Coll Sci & Technol, Kennedy Inst Rheumatol, London, England
[5] Kings Coll London, Infect & Immun Res Grp, London WC2R 2LS, England
[6] Univ Essex, Dept Biol Sci, Colchester CO4 3SQ, Essex, England
基金
英国医学研究理事会;
关键词
Zfp36l1; VEGF; extraembryonic and intraembryonic vasculature;
D O I
10.1002/dvdy.20949
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The Zfp36l1 gene encodes a zinc finger-containing mRNA binding protein implicated in the posttranscriptional control of gene expression. Mouse embryos homozygous for a targeted mutation in the Zfp36l1 locus died mid-gestation and exhibited extraembryonic and intraembryonic vascular abnormalities and heart defects. In the developing placenta, there was a failure of the extraembryonic mesoderm to invaginate the trophoblast layer. The phenotype was associated with an elevated expression of vascular endothelial growth factor (VEGF)-A in the embryos and in embryonic fibroblasts cultured under conditions of both normoxia and hypoxia. VEGF-A overproduction by embryonic fibroblasts was not a consequence of changes in Vegf-a mRNA stability; instead, we observed enhanced association with polyribosomes, suggesting Zfp36l1 influences translational regulation. These data implicate Zfp36l1 as a negative regulator of Vegf-a gene activity during development.
引用
收藏
页码:3144 / 3155
页数:12
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