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Distribution of CTP:Phosphocholine Cytidylyltransferase (CCT) Isoforms: Identification of a New CCT beta Splice Variant
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...
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Published in: | The Journal of biological chemistry 1999-09, Vol.274 (38), p.26992-27001 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | 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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ISSN: | 0021-9258 |
DOI: | 10.1074/jbc.274.38.26992 |