Distribution of CTP:phosphocholine cytidylyltransferase (CCT) isoforms -: Identification of a new CCTβ splice variant

被引:126
作者
Lykidis, A
Baburina, I
Jackowski, S
机构
[1] St Jude Childrens Res Hosp, Dept Biochem, Memphis, TN 38105 USA
[2] Univ Tennessee, Dept Biochem, Memphis, TN 38163 USA
关键词
D O I
10.1074/jbc.274.38.26992
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
CTP:phosphocholine cytidylyltransferase is a major regulator of phosphatidylcholine biosynthesis. A single isoform, CCT alpha, has been studied extensively and a second isoform, CCT beta, was recently identified. We identify and characterize a third cDNA, CCT beta 2, that differs from CCT beta 1 at the carboxyl-terminal end and is predicted to arise as a splice variant of the CCT beta gene. Like CCT alpha, CCT beta 2 is heavily phosphorylated in vivo, in contrast to CCT beta 1. CCT beta 1 and CCT beta 2 mRNAs were differentially expressed by the human tissues examined, whereas CCT alpha was more uniformly represented. Using isoform-specific antibodies, both CCT beta 1 and CCT beta 2 localized to the endoplasmic reticulum of cells, in contrast to CCT alpha which resided in the nucleus in addition to associating with the endoplasmic reticulum. CCT beta 2 protein has enzymatic activity in vitro and was able to complement the temperature-sensitive cytidylyltransferase defect in CHO58 cells, just as CCT alpha and CCT beta 1 supporting proliferation at the nonpermissive conditions. Overexpression experiments did not reveal discrete physiological functions for the three isoforms that catalyze the same biochemical reaction; however, the differential cellular localization and tissue-specific distribution suggest that CCT beta 1 and CCT beta 2 may play a role that is distinct from ubiquitously expressed CCT alpha.
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页码:26992 / 27001
页数:10
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