NELF Potentiates Gene Transcription in the Drosophila Embryo

被引:23
|
作者
Wang, Xiaoling [1 ,2 ]
Hang, Saiyu [1 ,2 ]
Prazak, Lisa [3 ]
Gergen, J. Peter [1 ,2 ]
机构
[1] SUNY Stony Brook, Dept Biochem & Cell Biol, Stony Brook, NY 11794 USA
[2] SUNY Stony Brook, Ctr Dev Genet, Grad Program Biochem & Struct Biol, Stony Brook, NY 11794 USA
[3] SUNY Stony Brook, Grad Program Mol & Cellular Biol, Stony Brook, NY 11794 USA
来源
PLOS ONE | 2010年 / 5卷 / 07期
基金
美国国家科学基金会;
关键词
POLYMERASE-II ELONGATION; RNA-POLYMERASE; FUSHI-TARAZU; CELL FATE; IN-VIVO; EXPRESSION; MELANOGASTER; SEGMENTATION; COFACTOR; PROMOTER;
D O I
10.1371/journal.pone.0011498
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
A hallmark of genes that are subject to developmental regulation of transcriptional elongation is association of the negative elongation factor NELF with the paused RNA polymerase complex. Here we use a combination of biochemical and genetic experiments to investigate the in vivo function of NELF in the Drosophila embryo. NELF associates with different gene promoter regions in correlation with the association of RNA polymerase II (Pol II) and the initial activation of gene expression during the early stages of embryogenesis. Genetic experiments reveal that maternally provided NELF is required for the activation, rather than the repression of reporter genes that emulate the expression of key developmental control genes. Furthermore, the relative requirement for NELF is dictated by attributes of the flanking cis-regulatory information. We propose that NELF-associated paused Pol II complexes provide a platform for high fidelity integration of the combinatorial spatial and temporal information that is central to the regulation of gene expression during animal development.
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页数:8
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