A unique isoform of phospholipase Cβ4 highly expressed in the cerebellum and eye

被引:21
作者
Adamski, FM
Timms, KM
Shieh, BH
机构
[1] Vanderbilt Univ, Dept Pharmacol, Nashville, TN 37232 USA
[2] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 1999年 / 1444卷 / 01期
关键词
PLC beta 4; alternative splicing; retina; cerebellum;
D O I
10.1016/S0167-4781(98)00260-7
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
We report a unique isoform of PLC beta 4 in rat, PLC beta 4c, that has an additional 37-nucleotide exon inserted between nucleotides 3459-3460 of the previously published PLC beta 4a coding sequence. This insertion results in replacement of 22 amino acid residues at the carboxyl terminal tail of PLC beta 4a with 41 unique residues. A human EST for PLC beta 4 also contains this exon and this exon was mapped to within a 5.5 kb intron of the human PLC beta 4 gene. PLC beta 4c is the third PLC beta 4 isoform to be identified which has a unique carboxyl-terminal tail. PLC beta 4b differs from PLC beta 4a by truncation 162 amino acid residues from the carboxyl terminus which are replaced with 10 distinct amino acid residues. Reverse transcription-polymerase chain reaction experiments show that both PLC beta 4a and PLC beta 4c mRNA are expressed throughout the rat brain and that PLC beta 4c mRNA is highly expressed in the eye and cerebellum. RNase protection assays demonstrate that both PLC beta 4a and PLC beta 4c transcripts are abundant in the cerebellum. The different carboxyl terminal tails of PLC beta 4 isoforms may allow for differential targeting and subcellular localization, contributing to regulation of PLC beta 4-mediated signal transduction. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:55 / 60
页数:6
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