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Tn5401, a new class II transposable element from Bacillus thuringiensis.

机译:Tn5401,苏云金芽胞杆菌的一种新的II类转座因子。

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摘要

A new class II (Tn3-like) transposable element, designated Tn5401, was recovered from a sporulation-deficient variant of Bacillus thuringiensis subsp. morrisoni EG2158 following its insertion into a recombinant plasmid. Sequence analysis of the insert revealed a 4,837-bp transposon with two large open reading frames, in the same orientation, encoding proteins of 36 kDa (306 residues) and 116 kDa (1,005 residues) and 53-bp terminal inverted repeats. The deduced amino acid sequence for the 36-kDa protein shows 24% sequence identity with the TnpI recombinase of the B. thuringiensis transposon Tn4430, a member of the phage integrase family of site-specific recombinases. The deduced amino acid sequence for the 116-kDa protein shows 42% sequence identity with the transposase of Tn3 but only 28% identity with the TnpA transposase of Tn4430. Two small open reading frames of unknown function, designated orf1 (85 residues) and orf2 (74 residues), were also identified. Southern blot analysis indicated that Tn5401, in contrast to Tn4430, is not commonly found among different subspecies of B. thuringiensis and is not typically associated with known insecticidal crystal protein genes. Transposition was studied with B. thuringiensis by using plasmid pEG922, a temperature-sensitive shuttle vector containing Tn5401. Tn5401 transposed to both chromosomal and plasmid target sites but displayed an apparent preference for plasmid sites. Transposition was replicative and resulted in the generation of a 5-bp duplication at the target site. Transcriptional start sites within Tn5401 were mapped by primer extension analysis. Two promoters, designated PL and PR, direct the transcription of orf1-orf2 and tnpI-tnpA, respectively, and are negatively regulated by TnpI. Sequence comparison of the promoter regions of Tn5401 and Tn4430 suggests that the conserved sequence element ATGTCCRCTAAY mediates TnpI binding and cointegrate resolution. The same element is contained within the 53-bp terminal inverted repeats, thus accounting for their unusual lengths and suggesting an additional role for TnpI in regulating Tn5401 transposition.
机译:从苏云金芽孢杆菌亚种的芽孢形成缺陷的变体中回收了一种新的II类(Tn3样)转座元件,命名为Tn5401。插入到重组质粒中之后的morrisoni EG2158。插入片段的序列分析显示,一个4837 bp的转座子具有两个大的开放阅读框,方向相同,编码36 kDa(306个残基)和116 kDa(1005个残基)和53 bp末端反向重复序列的蛋白质。推导的36 kDa蛋白氨基酸序列与苏云金芽胞杆菌转座子Tn4430的TnpI重组酶具有24%的序列同一性,该酶是位点特异性重组酶的噬菌体整合酶家族的成员。推导的116-kDa蛋白氨基酸序列与Tn3的转座酶显示42%的序列同一性,但与Tn4430的TnpA转座酶仅28%的同一性。还鉴定了两个功能未知的小型开放阅读框,分别为orf1(85个残基)和orf2(74个残基)。 Southern印迹分析表明,与Tn4430相比,Tn5401在苏云金芽孢杆菌的不同亚种中并不常见,并且通常不与已知的杀虫晶体蛋白基因相关。通过使用质粒TEG922(一种含有Tn5401的温度敏感性穿梭载体)研究了苏云金芽胞杆菌的转座。 Tn5401转座到染色体和质粒目标位点,但表现出明显的质粒位点优先。转座是复制性的,并导致在靶位点产生5-bp的复制。通过引物延伸分析将Tn5401内的转录起始位点作图。两个启动子,分别称为PL和PR,分别指导orf1-orf2和tnpI-tnpA的转录,并受TnpI负调控。 Tn5401和Tn4430启动子区域的序列比较表明,保守的序列元件ATGTCCRCTAAY介导TnpI结合并共同整合分辨率。相同的元件包含在53 bp的末端反向重复序列中,因此说明了它们的异常长度,并暗示了TnpI在调节Tn5401转座中的其他作用。

著录项

  • 作者

    Baum, J A;

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  • 年度 1994
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  • 原文格式 PDF
  • 正文语种 en
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