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首页> 外文期刊>Molecular and Cellular Biology >The L1Tc C-Terminal Domain from Trypanosoma cruzi Non-Long Terminal Repeat Retrotransposon Codes for a Protein That Bears Two C2H2 Zinc Finger Motifs and Is Endowed with Nucleic Acid Chaperone Activity
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The L1Tc C-Terminal Domain from Trypanosoma cruzi Non-Long Terminal Repeat Retrotransposon Codes for a Protein That Bears Two C2H2 Zinc Finger Motifs and Is Endowed with Nucleic Acid Chaperone Activity

机译:L1Tc C末端域从克鲁斯锥虫非长末端重复反转录转座子编码的蛋白质,带有两个C2H2锌手指基序,并具有核酸伴侣活性

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L1Tc, a non-long terminal repeat retrotransposon from Trypanosoma cruzi, is a 4.9-kb actively transcribed element which contains a single open reading frame coding for the machinery necessary for its autonomous retrotransposition. In this paper, we analyze the protein encoded by the L1Tc 3′ region, termed C2-L1Tc, which contains two zinc finger motifs similar to those present in the TFIIIA transcription factor family. C2-L1Tc binds nucleic acids with different affinities, such that RNA > tRNA > single-stranded DNA > double-stranded DNA, without any evidence for sequence specificity. C2-L1Tc also exhibits nucleic acid chaperone activity on different DNA templates that may participate in the mechanism of retrotransposition of the element. C2-L1Tc promotes annealing of complementary oligonucleotides, prevents melting of perfect DNA duplexes, and facilitates the strand exchange between DNAs to form the most stable duplex DNA in competitive displacement assays. Mapping of regions of C2-L1Tc using specific peptides showed that nucleic acid chaperone activity required a short basic sequence accompanied by a zinc finger motif or by another basic region such as RRR. Thus, a short basic polypeptide containing the two C2H2 motifs promotes formation of the most stable duplex DNA at a concentration only three times higher than that required for C2-L1Tc.
机译:L1Tc是一种来自锥虫(Trypanosoma cruzi)的非长末端重复反转录转座子,是一个4.9 KB的主动转录元件,其中包含一个单一的开放阅读框,编码其自主逆转录所需的机制。在本文中,我们分析了由L1Tc 3'区域编码的蛋白质,称为C2-L1Tc,该蛋白质包含两个类似于TFIIIA转录因子家族中存在的锌指基序。 C2-L1Tc结合具有不同亲和力的核酸,使得RNA> tRNA>单链DNA>双链DNA,而没有任何序列特异性的证据。 C2-L1Tc在不同的DNA模板上也表现出核酸伴侣活性,可能参与该元件的逆转座子机制。 C2-L1Tc促进互补寡核苷酸的退火,防止完美的DNA双链体融化,并促进DNA之间的链交换,从而在竞争性置换分析中形成最稳定的双链体DNA。使用特定肽对C2-L1Tc区域进行定位显示,核酸分子伴侣活性需要一个短的基本序列,并带有一个锌指基序或另一个基本区域,例如RRR。因此,含有两个C 2 H 2 基序的短碱性多肽可促进最稳定的双链DNA的形成,其浓度仅比C2-L1Tc所需的浓度高三倍。

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