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Selective constraint and the evolution of the RNA polymerase II C-terminal domain

机译:RNA聚合酶II C末端域的选择性约束和演变

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摘要

The C-terminal domain (CTD) of the large subunit (Rpb1) of RNA polymerase II has a Tyrosine-Serine-Proline-Threonine-Serine-Proline-Serine repeat structure in many eukaryotes. Chemical modifications of these residues play a central role in the regulation and coordination of the events of transcription/However, substantial variability in the presence and regularity of repeat arrays exists between eukaryote taxa. Following a survey of CTD structure from diverse eukaryote species, two hypotheses were tested relating to repeat structure and the action of selection on the CTD. First, it was found that degenerated repeat structure is associated with lower serine and proline frequencies in some eukaryote taxa but not in others. Second, maximum likelihood models of the evolution of Rpbl in a number of species groups found that purifying selection on the non-repetitive CTD of several Leishmania species was substantially lower than for the rest of Rpbl, whereas purifying selection in a number of species groups containing repeat arrays was usually as high or nearly as high as for the rest of Rpbl. Characterization of CTD structure for a larger number of species than has been completed previously also revealed a greater diversity of CTD structures in eukaryotes than previously known, along with loss of repeat structure in the animals and fungi, two taxa where it has not previously been known. These results suggest that loss of CTD repeat structure has been an important aspect of RNA polymerase II evolution in diverse eukaryotes.
机译:RNA聚合酶II的大亚基(Rpb1)的C末端结构域(CTD)在许多真核生物中具有酪氨酸-丝氨酸-脯氨酸-苏氨酸-丝氨酸-丝氨酸-脯氨酸-丝氨酸的重复结构。这些残基的化学修饰在转录事件的调节和协调中起着核心作用。然而,在真核生物类群之间存在重复阵列的存在和规律性存在很大差异。在对来自各种真核生物物种的CTD结构进行调查之后,测试了两个关于重复结构和选择对CTD作用的假说。首先,发现在某些真核生物类群中,退化的重复结构与较低的丝氨酸和脯氨酸频率有关,而在其他真核生物中则与较低的丝氨酸和脯氨酸频率有关。其次,在多个物种组中Rpbl进化的最大似然模型发现,在几个利什曼原虫物种的非重复CTD上纯化选择的能力明显低于其余Rpbl物种,而在包含重复阵列通常与Rpbl的其余部分一样高或几乎一样高。对比以前更多的物种进行CTD结构鉴定的结果还显示,真核生物中CTD结构的多样性比以前已知的更大,并且动物和真菌(两个分类群中以前未知的)的重复结构丧失。这些结果表明,CTD重复结构的缺失已成为各种真核生物中RNA聚合酶II进化的重要方面。

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