首页> 外文期刊>Molecular and Cellular Biology >Localization of sequences required in cis for yeast Ty1 element transposition near the long terminal repeats: analysis of mini-Ty1 elements.
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Localization of sequences required in cis for yeast Ty1 element transposition near the long terminal repeats: analysis of mini-Ty1 elements.

机译:靠近长末端重复序列的酵母Ty1元素转座所需的顺式序列的定位:mini-Ty1元素分析。

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In order to identify and characterize sequences within Ty1 elements which are required in cis for transposition, a series of mini-Ty1 plasmids were constructed and tested for transposition. Mini-Ty1s are deletion mutants of the Ty1-H3 element; Ty1 gene products required for transposition are supplied in trans from a helper Ty1 which has intact open reading frames but lacks a 3' long terminal repeat (LTR) and therefore cannot transpose itself. Up to 5 kilobase pairs of internal sequences of the 6-kilobase-pair-long Ty1 element can be deleted without a significant effect on transposition. The smallest mini-Ty1 element capable of transposition contains the 3' LTR and the transcribed portion of the 5' LTR, 285 base pairs (bp) of internal sequence 3' to the 5' LTR, and 23 bp of internal sequence 5' to the 3' LTR. We conclude that Ty1-encoded proteins can act in trans and that cis-acting sequences in Ty1-H3 are all within or near the LTRs. Further deletion of the 285-bp internal sequence adjacent to the 5' LTR significantly reduced transposition frequency, and the mini-Ty1 RNA produced failed to be packaged into the viruslike particles efficiently. Surprisingly, several nonhomologous cellular mRNAs were also associated with viruslike particles.
机译:为了鉴定和表征顺式转座所需的Ty1元件内的序列,构建了一系列mini-Ty1质粒并测试了转座。 Mini-Ty1s是Ty1-H3元件的缺失突变体;转座所需的Ty1基因产物由具有完整开放阅读框但缺乏3'长末端重复序列(LTR)的辅助Ty1反式提供,因此无法自我转座。最多可以删除5个碱基对长的Ty1元素的内部序列的5个碱基对,而对转座没有明显影响。能够转座的最小mini-Ty1元件包含3'LTR和5'LTR的转录部分,285个碱基对(bp)的内部序列3'至5'LTR以及23 bp的内部序列5'至3'LTR。我们得出的结论是,Ty1编码的蛋白可以反式作用,而Ty1-H3中的顺式作用序列都在LTR内或附近。 5'LTR附近的285 bp内部序列的进一步删除显着降低了转座频率,并且产生的mini-Ty1 RNA无法有效地包装到病毒样颗粒中。令人惊讶地,几种非同源细胞mRNA也与病毒样颗粒有关。

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