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弓形虫 Spt5 样转录延伸因子的特征。

Characterization of Toxoplasma gondii Spt5 like transcription elongation factor.

机构信息

Department of Animal Biology, School of Life Sciences, University of Hyderabad, Hyderabad, India.

National Institute of Animal Biotechnology, Hyderabad, India.

出版信息

Biochim Biophys Acta Gene Regul Mech. 2019 Feb;1862(2):184-197. doi: 10.1016/j.bbagrm.2019.01.003. Epub 2019 Jan 29.

DOI:10.1016/j.bbagrm.2019.01.003
PMID:30707945
Abstract

Elongation has emerged as a highly regulated step in the multistage process of transcription. Control of gene expression mediated through transcription elongation remains an unexplored area of study in Toxoplasma gondii where the demands of complex lifecycle necessitate a regulated transcription program. Here, we elucidate the central role of Spt5 homolog in T. gondii mRNA transcription. We demonstrate that TgSpt5 functions in conjunction with a small zinc finger protein TgSpt4. TgSpt5 interacts with TgRpb1, the largest subunit of RNA polymerase II and associates with actively transcribed genes. Enrichment of TgSpt5 towards the 3' end of genes coinciding with P-Ser2 form of RNAPII, a marker of active elongation further underscores its pivotal role in transcription. TgSpt5 undergoes phosphorylation mediated through Toxoplasma Cdk9 homolog, TgCrk9, which appears crucial for its function. Inhibition of TgCrk9, which also regulates RNAPII by differential phosphorylation of its C terminal domain, results in loss of TgSpt5 enrichment at 3' sites of the genes and an overall repressive effect on parasite progression. TgSpt5 along with TgSpt4 could successfully complement the loss of function mutations in yeast counterparts emphasizing its functional significance. Together, the results highlight the possible role of TgSpt5 in transcript elongation regulated through phosphorylation by TgCrk9.

摘要

延伸已成为转录多阶段过程中高度调控的步骤。通过转录延伸介导的基因表达控制仍然是刚地弓形虫研究中一个未探索的领域,在该领域中,复杂生命周期的需求需要一个受调控的转录程序。在这里,我们阐明了 Spt5 同源物在刚地弓形虫 mRNA 转录中的核心作用。我们证明 TgSpt5 与一个小锌指蛋白 TgSpt4 共同发挥作用。TgSpt5 与 RNA 聚合酶 II 的最大亚基 TgRpb1 相互作用,并与转录活跃的基因结合。TgSpt5 向基因 3' 末端的富集与 RNAPII 的 P-Ser2 形式一致,这是活跃延伸的标志,进一步强调了其在转录中的关键作用。TgSpt5 通过刚地弓形虫 Cdk9 同源物 TgCrk9 介导的磷酸化作用,TgCrk9 似乎对其功能至关重要。TgCrk9 的抑制作用,通过其 C 端结构域的差异磷酸化来调节 RNAPII,导致 TgSpt5 在基因 3' 位点的富集丧失,并对寄生虫的进展产生整体抑制作用。TgSpt5 与 TgSpt4 一起可以成功地补充酵母对应物功能丧失突变,强调了其功能意义。总之,这些结果突出了 TgSpt5 在 TgCrk9 通过磷酸化调节的转录延伸中的可能作用。

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