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摇蚊Balbiani环DNA序列的结构分析

A structural analysis of Balbiani ring dna sequences in Chironomus tentans.

作者信息

Degelmann A, Hollenberg C P

出版信息

Chromosoma. 1981;83(3):295-313. doi: 10.1007/BF00327354.

Abstract

The Balbiani rings in the salivary gland polytene chromosomes of Chironomus tentans include the most active structural genes in this organ. Two of them (BR1 and BR2) contain repetitive sequences and are transcribed into giant RNA molecules. On Southern blots of restriction digests, we have identified fragments of genomic DNA which contain BR sequences. One of these fragments with a length of about 150 bp has been cloned and shown to hybridize preferentially to the BR1 transcription unit. Determination of its nucleotide sequence revealed several recognition sites for restriction enzymes which cleave the giant BR gene(s) into small pieces of approximately 240 bp. It is concluded that the cloned fragment represents part of the basic 240 bp repeat unit of a BR1 gene. Data obtained from partial restriction digests using the cloned DNA segment as a probe indicate that probably the entire BR1 gene comprises tandem repeats of 240 bp. Evidence is presented that the cloned BR1 sequence significantly cross-hybridizes to BR2 and to a lesser extent to BR6. BR2 sequences are present on a MboI fragment of 40 kb and seem to be organized in a very similar way as found for the BR1 gene.

摘要

摇蚊唾腺多线染色体中的巴尔比亚尼环包含该器官中最活跃的结构基因。其中两个(BR1和BR2)含有重复序列,并转录成巨大的RNA分子。在限制性酶切消化的Southern印迹上,我们鉴定出了包含BR序列的基因组DNA片段。其中一个长度约为150 bp的片段已被克隆,并显示出优先与BR1转录单元杂交。其核苷酸序列的测定揭示了几种限制酶的识别位点,这些酶将巨大的BR基因切割成约240 bp的小片段。结论是,克隆的片段代表BR1基因基本240 bp重复单元的一部分。使用克隆的DNA片段作为探针从部分限制性酶切消化中获得的数据表明,整个BR1基因可能由240 bp的串联重复组成。有证据表明,克隆的BR1序列与BR2有显著的交叉杂交,与BR6的交叉杂交程度较小。BR2序列存在于一个40 kb的MboI片段上,其组织方式似乎与BR1基因非常相似。

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