Synthetic in vivo validation of gene network circuitry

被引:16
作者
Damle, Sagar S. [1 ]
Davidson, Eric H. [1 ]
机构
[1] CALTECH, Div Biol, Pasadena, CA 91125 USA
基金
美国国家卫生研究院;
关键词
reengineering development; Strongylocentrotus purpuratus; SEA-URCHIN EMBRYO; CIS-REGULATORY CONTROL; SPECIFICATION; EXPRESSION; MICROMERES; PURPURATUS; LINEAGE; MEMBER; CELLS; DNA;
D O I
10.1073/pnas.1119905109
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Embryonic development is controlled by networks of interacting regulatory genes. The individual linkages of gene regulatory networks (GRNs) are customarily validated by functional cis-regulatory analysis, but an additional approach to validation is to rewire GRN circuitry to test experimentally predictions derived from network structure. Here we use this synthetic method to challenge specific predictions of the sea urchin embryo endomesoderm GRN. Expression vectors generated by in vitro recombination of exogenous sequences into BACs were used to cause elements of a nonskeletogenic mesoderm GRN to be deployed in skeletogenic cells and to detect their effects. The result of reengineering the regulatory circuitry in this way was to divert the developmental program of these cells from skeletogenesis to pigment cell formation, confirming a direct prediction of the GRN. In addition, the experiment revealed previously undetected cryptic repression functions.
引用
收藏
页码:1548 / 1553
页数:6
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