TISSUE DISTRIBUTION AND INTRACELLULAR-LOCALIZATION OF THE 75-KDA INOSITOL POLYPHOSPHATE 5-PHOSPHATASE

被引:23
作者
SPEED, CJ [1 ]
MATZARIS, M [1 ]
BIRD, PI [1 ]
MITCHELL, CA [1 ]
机构
[1] MONASH UNIV SCH MED, BOX HILL HOSP, DEPT MED, MELBOURNE, VIC, AUSTRALIA
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1995年 / 234卷 / 01期
关键词
INOSITOL POLYPHOSPHATE 5-PHOSPHATASE; INOSITOL 1,4,5-TRISPHOSPHATE;
D O I
10.1111/j.1432-1033.1995.216_c.x
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
The 75-kDa inositol polyphosphate 5-phosphatase (75-kDa 5-phosphatase) hydrolyses several important mediators of intracellular calcium homeostasis, including inositol 1,4,5-trisphosphate [Ins(1,4,5)P-3], inositol 1,3,4,5-tetrakisphosphate [Ins(1,3,4,5)P-4] and phosphatidylinositol 4,5-bisphosphate [PtdIns(4,5)P-2]. Northern analysis of various human tissues revealed the 75-kDa 5-phosphatase has a ubiquitous expression, where differential splicing may occur in specific tissues. Prominent expression of a 4.4-kb transcript was noted in human lung, thymus, testes and placenta, and a 4.6-kb transcript was observed in heart, brain, kidney, ovary and colon. Determination of the intracellular location of the enzyme by indirect immunofluorescence, demonstrated that the 75-kDa 5-phosphatase was associated with mitochondrial and cytosolic cellular compartments. Immunoprecipitation of the total cell homogenate of human lung carcinoma cells (A549) with anti-(recombinant 75-kDa 5-phosphatase) antibodies revealed that the 75-kDa 5-phosphatase is the major PtdIns(4,5)P-2 5-phosphatase in this cell line. Analysis of PtdIns(4,5)P-2 5-phos phatase activity in subcellular fractions of A549 cells revealed peak 75-kDa 5-phosphatase enzyme activity in the cytosolic and mitochondrial enriched fractions. Immunoblot analysis further confirmed the mitochondrial location of the enzyme. This study demonstrates the tissue distribution and intracellular location of the 75-kDa 5-phosphatase and reveals a novel location for an enzyme involved in phosphatidylinositol turnover.
引用
收藏
页码:216 / 224
页数:9
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