Molecular analysis of the cDNA and genomic DNA encoding mouse RNA helicase A

被引:24
作者
Lee, CG
Eki, T
Okumura, K
Soares, VD
Hurwitz, J
机构
[1] Mem Sloan Kettering Canc Ctr, Grad Program Mol Biol, New York, NY 10021 USA
[2] RIKEN, Inst Phys & Chem Res, Tsukuba Life Sci Ctr, Cellular Physiol Lab, Tsukuba, Ibaraki 305, Japan
[3] Mie Univ, Fac Bioresources, Tsu, Mie 514, Japan
基金
日本科学技术振兴机构;
关键词
D O I
10.1006/geno.1997.5139
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
RNA helicase A is an enzyme that possesses both RNA and DNA helicase activities. In this report, we describe the isolation of a mouse cDNA encoding RNA helicase A, The deduced amino acid sequence derived from mouse RNA helicase A cDNA exhibits 87 and 47% identity to its human and Drosophila homologs, respectively, Using Southern blot analysis employing a mouse backcross panel, we have assigned the mouse RNA helicase A gene to chromosome 1, mapping near the D1Bir20 locus at MGD position 67. Northern blot and primer extension analyses indicate that, although its level is variable, RNA helicase A appears to be expressed from a single transcription start site in all tissues tested. Sequence analysis of the upstream genomic DNA revealed that the promoter region lacks a TATA box and contains two high-affinity sites for Spl, one ISRE, a binding site for interferon regulatory factor, and three AP2-binding sites, These findings suggest that the transcriptional regulation of the RNA helicase A gene is complex. (C) 1998 Academic Press.
引用
收藏
页码:365 / 371
页数:7
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