Chromatin-remodeling complex specificity and embryonic vascular development

被引:11
|
作者
Curtis, Carol D. [1 ]
Davis, Reema B. [1 ,2 ]
Ingram, Kyle G. [1 ,2 ]
Griffin, Courtney T. [1 ,2 ]
机构
[1] Oklahoma Med Res Fdn, Cardiovasc Biol Res Program, Oklahoma City, OK 73104 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Dept Cell Biol, Oklahoma City, OK 73190 USA
基金
美国国家卫生研究院;
关键词
ATP-dependent chromatin-remodeling complex; Embryo; Angiogenesis; Blood vessel; SWI/SNF; NuRD; ENZYME BRG1; GENE-EXPRESSION; SWI/SNF; DIFFERENTIATION; TRANSCRIPTION; MI-2-BETA; ROLES; COMPONENT; ATPASE; MORPHOGENESIS;
D O I
10.1007/s00018-012-1023-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vascular development is a dynamic process that relies on the coordinated expression of numerous genes, but the factors that regulate gene expression during blood vessel development are not well defined. ATP-dependent chromatin-remodeling complexes are gaining attention for their specific temporal and spatial effects on gene expression during vascular development. Genetic mutations in chromatin-remodeling complex subunits are revealing roles for the complexes in vascular signaling pathways at discrete developmental time points. Phenotypic analysis of these models at various stages of vascular development will continue to expand our understanding of how chromatin remodeling impacts new blood vessel growth. Such research could also provide novel therapeutic targets for the treatment of vascular pathologies.
引用
收藏
页码:3921 / 3931
页数:11
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