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果蝇三个发育调控基因的支架结合区域与上游/增强子元件的共定位。

Cohabitation of scaffold binding regions with upstream/enhancer elements of three developmentally regulated genes of D. melanogaster.

作者信息

Gasser S M, Laemmli U K

出版信息

Cell. 1986 Aug 15;46(4):521-30. doi: 10.1016/0092-8674(86)90877-9.

Abstract

We find DNA fragments attached to the nuclear scaffold (SARs) both 5' and 3' of three Drosophila genes, defining looped domains ranging from 4.5 to 13 kb. For the two-promoter-containing gene Adh (alcohol dehydrogenase), we find two upstream and two downstream SARs. For Sgs-4, the 5' SAR covers 866 bp immediately upstream of the transcript, and in the case of fushi tarazu, the 5' SAR is found on a small fragment 4.8 kb upstream of the start of transcription. These four upstream scaffold-attached fragments comap with enhancer-like regulatory sequences. Sequence analysis of five upstream SARs reveals clusters of sequences closely related to the cleavage consensus of topoisomerase II, several copies of a specific 10 bp A-rich sequence (AATAAATCAAA), and another 10 bp T-rich stretch.

摘要

我们在三个果蝇基因的5'端和3'端均发现了附着于核支架(SARs)的DNA片段,这些片段界定了范围从4.5至13 kb的环状结构域。对于含有两个启动子的基因Adh(乙醇脱氢酶),我们发现了两个上游和两个下游SARs。对于Sgs-4基因,5'端的SAR覆盖了转录本上游紧邻的866 bp区域;而对于ftz(分节基因)基因,5'端的SAR位于转录起始点上游4.8 kb的一个小片段上。这四个上游附着于支架的片段与增强子样调控序列共定位。对五个上游SARs的序列分析揭示了与拓扑异构酶II切割共有序列密切相关的序列簇、特定的富含A的10 bp序列(AATAAATCAAA)的多个拷贝以及另一个富含T的10 bp片段。

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