A SINGLE ISOFORM OF THE NA+/K+-ATPASE ALPHA-SUBUNIT IN DIPTERA - EVIDENCE FROM CHARACTERIZATION OF THE FIRST EXTRACELLULAR DOMAIN

被引:6
作者
EMERY, AM
READY, PD
BILLINGSLEY, PF
DJAMGOZ, MBA
机构
[1] NAT HIST MUSEUM, DEPT ENTOMOL, DIV MOLEC SYSTEMAT, MOLEC SYSTEMAT LAB, LONDON SW7 5BD, ENGLAND
[2] UNIV LONDON IMPERIAL COLL SCI TECHNOL & MED, DEPT BIOL, LONDON, ENGLAND
关键词
NA+/K+-ATPASE; ISOFORMS; ALPHA-SUBUNIT; DIPTERA; GENOMIC DNA; PHYLOGENY;
D O I
10.1111/j.1365-2583.1995.tb00024.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 first extracellular domain of the alpha-subunit of the Na+/K+-ATPase (sodium/potassium pump) is functionally important, affecting sensitivity of the enzyme to cardiac glycosides (e.g. ouabain) and being implicated in the transport of K+. This domain is also variable among mammalian isoforms of the alpha-subunit. Using PCR, we have isolated from seven insect species with contrasting physiologies a DNA fragment containing this region, in order to help determine whether tissue-specific expression might be associated with isoforms encoded by a gene family, as it is in mammals, A single sequence (with one ORF) characteristic of Na+/K+-ATPase was obtained from genomic DNA of each species, Only the fragment from Manduca sexta contained an intron, but at a location different to that found in mammals, For all Diptera so far characterized, the species phylogeny is the same as the alpha-subunit gene phylogeny (based on the sequences of the first extracellular domain and flanking transmembrane domains), The results strongly indicate a single, ouabain-sensitive isoform of the alpha-subunit of Na+/K+-ATPase is present in Diptera.
引用
收藏
页码:179 / 192
页数:14
相关论文
共 54 条
[1]   DIFFERENT OUABAIN SENSITIVITIES OF NA+/K+-ATPASE FROM POEKILOCERUS-BUFONIUS TISSUES AND A POSSIBLE PHYSIOLOGICAL COST [J].
ALROBAI, AA .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1993, 106 (04) :805-812
[2]   MOLECULAR-CLONING OF THE NA,K-ATPASE ALPHA-SUBUNIT IN DEVELOPING BRINE SHRIMP AND SEQUENCE COMPARISON WITH HIGHER ORGANISMS [J].
BAXTERLOWE, LA ;
JIAN, ZG ;
BERGSTROM, EE ;
HOKIN, LE .
FEBS LETTERS, 1989, 257 (01) :181-187
[3]   PHOSPHORYLATION OF THE CATALYTIC SUBUNIT OF NA+,K+-ATPASE INHIBITS THE ACTIVITY OF THE ENZYME [J].
BERTORELLO, AM ;
APERIA, A ;
WALAAS, SI ;
NAIRN, AC ;
GREENGARD, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (24) :11359-11362
[4]   APPROACHES TO VECTOR CONTROL - NEW AND TRUSTED .2. MOLECULAR TARGETS IN THE INSECT MIDGUT [J].
BILLINGSLEY, PF .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1994, 88 (02) :136-140
[5]   ADVANCES IN NA+,K+-ATPASE STUDIES - FROM PROTEIN TO GENE AND BACK TO PROTEIN [J].
BROUDE, NE ;
MODYANOV, NN ;
MONASTYRSKAYA, GS ;
SVERDLOV, ED .
FEBS LETTERS, 1989, 257 (01) :1-9
[6]   FUNCTIONAL EXPRESSION OF N-TERMINAL TRUNCATED ALPHA-SUBUNITS OF NA,K-ATPASE IN XENOPUS-LAEVIS OOCYTES [J].
BURGENERKAIRUZ, P ;
HORISBERGER, JD ;
GEERING, K ;
ROSSIER, BC .
FEBS LETTERS, 1991, 290 (1-2) :83-86
[7]   MUTATION OF A CYSTEINE IN THE 1ST TRANSMEMBRANE SEGMENT OF NA,K-ATPASE ALPHA SUBUNIT CONFERS OUABAIN RESISTANCE [J].
CANESSA, CM ;
HORISBERGER, JD ;
LOUVARD, D ;
ROSSIER, BC .
EMBO JOURNAL, 1992, 11 (05) :1681-1687
[8]  
CANFIELD VA, 1992, NEW BIOL, V4, P339
[9]  
CANTLEY LG, 1992, J BIOL CHEM, V267, P17271
[10]  
CRAMPTON GC, 1944, B BROOKLYN ENTOMOL S, V34, P1