Evolution of Insect Dorsoventral Patterning Mechanisms

被引:14
作者
Perry, M. W. [1 ]
Cande, J. D. [2 ]
Boettiger, A. N. [3 ]
Levine, M. [2 ]
机构
[1] Univ Calif Berkeley, Dept Integrat Biol, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Mol & Cell Biol, Div Genet Genom & Dev, Ctr Integrat Genom, 229 Stanley Hall, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Biophys Program, Berkeley, CA 94720 USA
来源
EVOLUTION: THE MOLECULAR LANDSCAPE | 2009年 / 74卷
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
RNA-POLYMERASE; GENE-EXPRESSION; DORSAL MORPHOGEN; DNA-BINDING; DROSOPHILA; PROTEIN; TRANSCRIPTION; ACTIVATION; SNAIL; GRADIENT;
D O I
10.1101/sqb.2009.74.021
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
The dorsoventral (DV) patterning of the early Drosophila embryo depends on Dorsal, a maternal sequence-specific transcription factor related to mammalian NF-kappa B. Dorsal controls DV patterning through the differential regulation of similar to 50 target genes in a concentration-dependent manner. Whole-genome methods, including ChIP-chip and ChIP-seq assays, have identified similar to 100 Dorsal target enhancers, and more than one-third of these have been experimentally confirmed via transgenic embryo assays. Despite differences in DV patterning among divergent insects, a number of the Dorsal target enhancers are located in conserved positions relative to the associated transcription units. Thus, the evolution of novel patterns of gene expression might depend on the modification of old enhancers, rather than the invention of new ones. As many as half of all Dorsal target genes appear to contain "shadow" enhancers: a second enhancer that directs the same or similar expression pattern as the primary enhancer. Preliminary studies suggest that shadow enhancers might help to ensure resilience of gene expression in response to environmental and genetic perturbations. Finally, most Dorsal target genes appear to contain RNA polymerase II (pol II) prior to their activation. Stalled pol II fosters synchronous patterns of gene activation in the early embryo. In contrast, DV patterning genes lacking stalled pol II are initially activated in an erratic or stochastic fashion. It is possible that stalled pol II confers fitness to a population by ensuring coordinate deployment of the gene networks controlling embryogenesis.
引用
收藏
页码:275 / 279
页数:5
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