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酵母TATA元件之间的功能差异。

Functional distinctions between yeast TATA elements.

作者信息

Harbury P A, Struhl K

机构信息

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115.

出版信息

Mol Cell Biol. 1989 Dec;9(12):5298-304. doi: 10.1128/mcb.9.12.5298-5304.1989.

Abstract

Although the yeast his3 promoter region contains two functional TATA elements, TR and TC, the GCN4 and GAL4 upstream activator proteins stimulate transcription only through TR. In combination with GAL4, an oligonucleotide containing the sequence TATAAA is fully sufficient for TR function, whereas almost all single-base-pair substitutions of this sequence abolish the ability of this element to activate transcription. Further analysis of these and other mutations of the TR element led to the following conclusions. First, sequences downstream of the TATAAA sequence are important for TR function. Second, a double mutant, TATTTA, can serve as a TR element even though the corresponding single mutation, TATTAA, is unable to do so. Third, three mutations have the novel property of being able to activate transcription in combination with GCN4 but not with GAL4; this finding suggests that activation by GCN4 and by GAL4 may not occur by identical mechanisms. From these observations, we address the question of whether there is a single TATA-binding factor required for the transcription of all genes.

摘要

尽管酵母his3启动子区域包含两个功能性TATA元件,即TR和TC,但GCN4和GAL4上游激活蛋白仅通过TR刺激转录。与GAL4结合时,含有TATAAA序列的寡核苷酸对于TR功能来说是完全足够的,而该序列几乎所有的单碱基对替换都会消除该元件激活转录的能力。对TR元件的这些及其他突变的进一步分析得出了以下结论。首先,TATAAA序列下游的序列对TR功能很重要。其次,双突变体TATTTA可以作为TR元件,尽管相应的单突变体TATTAA不能。第三,有三个突变具有能够与GCN4结合但不能与GAL4结合来激活转录的新特性;这一发现表明,GCN4和GAL4的激活机制可能不同。基于这些观察结果,我们探讨了是否存在一个所有基因转录都需要的单一TATA结合因子这一问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54dc/363694/474754ce096a/molcellb00060-0036-a.jpg

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