The proximal sequence element (PSE) plays a major role in establishing the RNA polymerase specificity of Drosophila U-snRNA genes

被引:40
作者
Jensen, RC
Wang, Y
Hardin, SB
Stumph, WE [1 ]
机构
[1] San Diego State Univ, Dept Chem, San Diego, CA 92182 USA
[2] San Diego State Univ, Inst Mol Biol, San Diego, CA 92182 USA
关键词
D O I
10.1093/nar/26.2.616
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Most small nuclear RNA (snRNA) genes are transcribed by RNA polymerase II, but some (e.g., U6) are transcribed by RNA polymerase iii, In vertebrates a TATA box at a fixed distance downstream of the proximal sequence element (PSE)acts as a dominant determinant for recruiting RNA polymerase III to U6 gene promoters. in contrast, vertebrate snRNA genes that contain a PSE but lack a TATA box are transcribed by RNA polymerase II, In plants, transcription of both classes of snRNA genes requires a TATA box in addition to an upstream sequence element (USE), and polymerase specificity is determined by the spacing between these two core promoter elements, in these examples, the PSE (or USE) is Interchangeable between the two classes of snRNA genes, Here we report the surprising finding that the Drosophila U1 and U6 PSEs cannot functionally substitute for each other; rather, determination of RNA polymerase specificity is an intrinsic property of:he PSE sequence itself, The alteration of two or three base pairs near the 3'-end of the U1 and US PSEs;was sufficient to switch the RNA polymerase specificity of Drosophila snRNA promoters in vitro, These findings reveal a novel mechanism for achieving RNA polymerase specificity at insect snRNA promoters.
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页码:616 / 622
页数:7
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