Cloning, characterization, and tissue distribution of mouse phosphodiesterase 7A1

被引:31
作者
Wang, P [1 ]
Wu, P [1 ]
Egan, RW [1 ]
Billah, MM [1 ]
机构
[1] Schering Plough Corp, Res Inst, Dept Allergy, Kenilworth, NJ 07033 USA
关键词
phosphodiesterase 7A1 (PDE7A1); cloning; expression; characterization; tissue distribution;
D O I
10.1006/bbrc.2000.3613
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 have cloned a cDNA representing mouse phosphodiesterases (PDE) 7A1. The open reading frame encodes a protein of 482 amino acids with a predicted molecular mass of 55417. Like human PDE7A variants, mouse PDE7A1 and A2 are 5' splice variants from a common gene. The distinct N-terminal sequence of mouse PDE7A1 is highly homologous to the corresponding sequence of human PDE7A1 with a similarity of 98% but not to that of mouse PDE7A2 (with a similarity of 12%), and is more hydrophilic than that of mouse PDE7A2. Mouse PDE7A1 expressed in SF9 cells has been compared with human PDE7A1 under identical conditions. Mouse PDE7A1 has a Km for cAMP of 0.2 mu M, an optimal pH of 7.5, an IC50 value of 14 mu M for 3-isobutyl-1-methylxanthine (IBMX), and is dependent on Mg2+ for activity. All these characteristics are very similar to those of human PDE7A1. In mice, PDE7A1 is expressed in tissues of the immune system (lymph node, thymus, spleen, and blood leukocyte), testis, brain, kidney and lung but not in skeletal muscle, heart, embryo, or liver, while PDE7A2 is expressed in skeletal muscle, heart, embryo, and kidney, but not in the other tissues. This tissue distribution profile is very similar to that in humans, and hence suggests that PDE7A1 and 7A2 might play a similar role in different species. (C) 2000 Academic Press.
引用
收藏
页码:1271 / 1277
页数:7
相关论文
共 24 条
[1]  
BAIROCH A, 1994, NUCLEIC ACIDS RES, V22, P3583
[2]   CYCLIC-NUCLEOTIDE PHOSPHODIESTERASES - FUNCTIONAL IMPLICATIONS OF MULTIPLE ISOFORMS [J].
BEAVO, JA .
PHYSIOLOGICAL REVIEWS, 1995, 75 (04) :725-748
[3]   Identification and tissue-specific expression of PDE7 phosphodiesterase splice variants [J].
Bloom, TJ ;
Beavo, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (24) :14188-14192
[4]  
Conti M, 2000, PROG NUCLEIC ACID RE, V63, P1
[5]   TOUCHDOWN PCR TO CIRCUMVENT SPURIOUS PRIMING DURING GENE AMPLIFICATION [J].
DON, RH ;
COX, PT ;
WAINWRIGHT, BJ ;
BAKER, K ;
MATTICK, JS .
NUCLEIC ACIDS RESEARCH, 1991, 19 (14) :4008-4008
[6]   Molecular cloning and characterization of a distinct human phosphodiesterase gene family: PDE11A [J].
Fawcett, L ;
Baxendale, R ;
Stacey, P ;
McGrouther, C ;
Harrow, I ;
Soderling, S ;
Hetman, J ;
Beavo, JA ;
Phillips, SC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3702-3707
[7]   RAPID PRODUCTION OF FULL-LENGTH CDNAS FROM RARE TRANSCRIPTS - AMPLIFICATION USING A SINGLE GENE-SPECIFIC OLIGONUCLEOTIDE PRIMER [J].
FROHMAN, MA ;
DUSH, MK ;
MARTIN, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (23) :8998-9002
[8]   Alternative splicing of the high affinity cAMP-specific phosphodiesterase (PDE7A) mRNA in human skeletal muscle and heart [J].
Han, P ;
Zhu, XY ;
Michaeli, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (26) :16152-16157
[9]  
HEIN J, 1990, METHOD ENZYMOL, V183, P626
[10]   Cloning and characterization of PDE7B, a cAMP-specific phosphodiesterase [J].
Hetman, JM ;
Soderling, SH ;
Glavas, NA ;
Beavo, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (01) :472-476