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TRF2 and the evolution of the bilateria

机译:TRF2与双语组织的演变

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摘要

The development of a complex body plan requires a diversity of regulatory networks. Here we consider the concept of TATA-box-binding protein (TBP) family proteins as ‘‘system factors’’ that each supports a distinct set of transcriptional programs. For instance, TBP activates TATA-box-dependent core promoters, whereas TBP-related factor 2 (TRF2) activates TATA-less core promoters that are dependent on a TCT or downstream core promoter element (DPE) motif. These findings led us to investigate the evolution of TRF2. TBP occurs in Archaea and eukaryotes, but TRF2 evolved prior to the emergence of the bilateria and subsequent to the evolutionary split between bilaterians and nonbilaterian animals. Unlike TBP, TRF2 does not bind to the TATA box and could thus function as a new system factor that is largely independent of TBP. We postulate that this TRF2-based system served as the foundation for new transcriptional programs, such as those involved in triploblasty and body plan development, that facilitated the evolution of bilateria.
机译:制定复杂的车身计划需要多种监管网络。在这里,我们将TATA盒结合蛋白(TBP)家族蛋白的概念视为“系统因子”,每个因子都支持一组独特的转录程序。例如,TBP激活依赖于TATA盒的核心启动子,而TBP相关因子2(TRF2)激活依赖于TCT或下游核心启动子元件(DPE)基序的无TATA的核心启动子。这些发现使我们研究了TRF2的进化。 TBP发生在古细菌和真核生物中,但是TRF2在双子出现之前和在双侧动物和非双侧动物之间的进化分裂之后进化。与TBP不同,TRF2不会绑定到TATA框,因此可以用作很大程度上独立于TBP的新系统因子。我们假设这个基于TRF2的系统为新的转录程序(如那些参与三叶母细胞和身体计划开发的程序)的基础,这些程序促进了双子的进化。

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