Analysis of mRNA expression and cloning of a novel plasma membrane Ca2+-ATPase splice variant in human heart

被引:1
作者
SantiagoGarcia, J
MasOliva, J
Saavedra, D
ZarainHerzberg, A
机构
[1] ST BONIFACE GEN HOSP, RES CTR, DIV CARDIOVASC SCI, WINNIPEG, MB R2H 2A6, CANADA
[2] UNIV MANITOBA, DEPT PHYSIOL, WINNIPEG, MB R2H 2A6, CANADA
[3] UNIV NACL AUTONOMA MEXICO, INST FISIOL CELULAR, DEPT BIOENERGET, MEXICO CITY 04510, DF, MEXICO
[4] HOSP GEN DR MANUEL GEA GONZALEZ, MEXICO CITY 14000, DF, MEXICO
关键词
development; cardiac muscle; placenta; sarcoplasmic reticulum; sarcolemma; plasma membrane; PMCA; SERCA2; SERCA3; cDNA cloning; PCR;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Four different plasma membrane Ca2+-ATPase (PMCA) genes and three sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA) genes have been previously cloned and characterized. In this study we have investigated the expression of the mRNA encoding the various PMCA and SERCA proteins in fetal and adult human heart and placenta by the reverse-transcriptase-polymerase-chain-reaction (RT-PCR) and cDNA cloning. We have found that PMCA1 and PMCA4 genes were expressed in 8-, 12- and 20-week fetal heart and in adult heart. PMCA2 gene was expressed at low levels in adult heart but was not detected in fetal heart. PMCA3 mRNA was not detected in the heart nor placenta. In contrast, the mRNA encoding SERCA2a, SERCA2b and SERCA3 were expressed in all cardiac developmental stages. Multiple alternatively spliced mRNA transcripts which differ at splice site A and B/C of the PMCA1, PMCA2 and PMCA4 genes were detected in the human heart. Interestingly, a novel tissue specific variant of the PMCA4 gene was detected in both fetal and adult human heart but not in placenta that accounts for about 30% of the total PMCA4 mRNA variant expression. DNA sequence analysis of this novel variant revealed that it corresponds to the equivalent of the PMCA1d variant and accordingly we have named it PMCA4d. We cloned and sequenced eight cDNA inserts encoding for the PMCA1 and PMCA4 variants from a fetal human heart cDNA library confirming that these are the two main PMCA genes expressed in cardiac muscle.
引用
收藏
页码:173 / 182
页数:10
相关论文
共 32 条
[1]   NEW CA2+ PUMP ISOFORMS GENERATED BY ALTERNATIVE SPLICING OF RPMCA2 MESSENGER-RNA [J].
ADAMO, HP ;
PENNISTON, JT .
BIOCHEMICAL JOURNAL, 1992, 283 :355-359
[2]   THE SARCO(ENDO)PLASMIC RETICULUM CA2+-ATPASE MESSENGER-RNA ISOFORM, SERCA-3, IS EXPRESSED IN ENDOTHELIAL AND EPITHELIAL-CELLS IN VARIOUS ORGANS [J].
ANGER, M ;
SAMUEL, JL ;
MAROTTE, F ;
WUYTACK, F ;
RAPPAPORT, L ;
LOMPRE, AM .
FEBS LETTERS, 1993, 334 (01) :45-48
[3]   2 CA-2+ ATPASE GENES - HOMOLOGIES AND MECHANISTIC IMPLICATIONS OF DEDUCED AMINO-ACID-SEQUENCES [J].
BRANDL, CJ ;
GREEN, NM ;
KORCZAK, B ;
MACLENNAN, DH .
CELL, 1986, 44 (04) :597-607
[4]  
BRANDL CJ, 1987, J BIOL CHEM, V262, P3768
[5]  
BRANDT P, 1994, J NEUROCHEM, V62, P799
[6]  
BRANDT P, 1992, J BIOL CHEM, V267, P4376
[7]  
BURK SE, 1992, J BIOL CHEM, V267, P19683
[8]  
BURK SE, 1989, J BIOL CHEM, V264, P18561
[9]   THE PLASMA-MEMBRANE CALCIUM-PUMP - FUNCTIONAL DOMAINS, REGULATION OF THE ACTIVITY, AND TISSUE-SPECIFICITY OF ISOFORM EXPRESSION [J].
CARAFOLI, E ;
STAUFFER, T .
JOURNAL OF NEUROBIOLOGY, 1994, 25 (03) :312-324
[10]  
CARAFOLI E, 1992, J BIOL CHEM, V267, P2115