SF4 and SFRS14, two related putative splicing factors on human chromosome 19p13.11

被引:27
作者
Sampson, ND [1 ]
Hewitt, JE [1 ]
机构
[1] Univ Nottingham, Queens Med Ctr, Inst Genet, Nottingham NG7 2UH, England
基金
英国生物技术与生命科学研究理事会;
关键词
G patch; SURP; arginine/serine rich; RNA binding; spliceosome;
D O I
10.1016/S0378-1119(02)01230-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The splicing of nascent mRNA precursors is an essential step for the expression of all intron-containing eukaryotic genes. Removal of intron sequences from nascent transcripts is mediated by the spliceosome, a large multicomponent complex. We describe here the identification of two genes encoding related, putative splicing factors on human chromosome 19p13.11, SF4 (splicing factor 4) and SFRS14 (splicing factor arginine/serine-rich 14). Both genes encode proteins containing a SURP motif; this domain is found in several splicing proteins including Drosophila alternative splicing regulator, suppressor-of-white-apricot (SWAP) and the yeast splicing factor, prp21p. In addition, SF4 and SFRS14 contain a G-patch domain at their C-termini, a motif present in a large number of eukaryotic RNA-binding proteins. SFRS14 also contains an N-terminal region that is rich in arginine/serine residues, suggesting SFRS14 is a novel member of the SR-related family of pre-mRNA processing factors. We have also identified the mouse orthologues of SF4 and SFRS14, based on conserved domain organization and high sequence similarity. Interestingly, SFRS14 undergoes alternative 3'-end processing events that are conserved between human and mouse, suggesting a functional significance. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:91 / 100
页数:10
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