CHROMOSOMAL MAPPING IN THE MOUSE OF 8 K+-CHANNEL GENES REPRESENTING THE 4 SHAKER-LIKE SUBFAMILIES SHAKER, SHAB, SHAW, AND SHAL

被引:33
作者
KLOCKE, R
ROBERDS, SL
TAMKUN, MM
GRONEMEIER, M
AUGUSTIN, A
ALBRECHT, B
PONGS, O
JOCKUSCH, H
机构
[1] UNIV BIELEFELD, DEV BIOL UNIT, D-33501 BIELEFELD, GERMANY
[2] VANDERBILT UNIV, SCH MED, DEPT MOLEC PHYSIOL & BIOPHYS, NASHVILLE, TN 37232 USA
[3] UNIV HAMBURG, CTR MOLEC NEUROBIOL, D-20246 HAMBURG, GERMANY
关键词
D O I
10.1016/S0888-7543(05)80358-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The four Shaker-like subfamilies of Shaker-, Shab-, Shaw-, and Shal-related K+ channels in mammals have been defined on the basis of their sequence homologies to the corresponding Drosophila genes. Using interspecific backcrosses between Mus musculus and Mus spretus, we have chromosomally mapped in the mouse the Shaker-related K+-channel genes Kcna1, Kcna2, Kcna4, Kcna5, and Kcna6; the Shab-related gene Kcnb1; the Shaw-related gene Kcnc4; and the Shal-related gene Kcnd2. The following localizations were determined: Chr 2, cen-Acra-Kcna4-Pax-6-a-Pck-1-Kras-3-Kcnb1 (corresponding human Chrs 11p and 20q, respectively); Chr 3, cen-Hao-2-(Kcna2, Kcnc4)-Amy-1 (human Chr 1); and Chr 6, cen-Cola-2-Met-Kcnd2-Cpa-Tcrb-adr/Clc-1-Hox-1.1-Myk-103-Raf-1-(Tpi-1, Kcna1, Kcna5, Kcna6) (human Chrs 7q and 12p, respectively). Thus, there is a cluster of at least three Shaker-related K+-channel genes on distal mouse Chr 6 and a cluster on Chr 2 that at least consists of one Shaker-related and one Shaw-related gene. The three other K+-channel genes are not linked to each other. The map positions of the different types of K+-channel genes in the mouse are discussed in relation to those of their homologs in man and to hereditary diseases of mouse and man that might involve K+ channels. © 1993 Academic Press, Inc.
引用
收藏
页码:568 / 574
页数:7
相关论文
共 66 条
[1]  
ALBRECHT B, 1993, RECEPTOR CHANNEL, V1, P99
[2]  
BARCHI R L, 1991, Current Biology, V1, P150, DOI 10.1016/0960-9822(91)90216-J
[3]   EVIDENCE OF GENETIC-HETEROGENEITY IN THE LONG QT SYNDROME [J].
BENHORIN, J ;
KALMAN, YM ;
MEDINA, A ;
TOWBIN, J ;
RAVEHAREL, N ;
DYER, TD ;
BLANGERO, J ;
MACCLUER, JW ;
KEREM, BS .
SCIENCE, 1993, 260 (5116) :1960-1962
[4]   STRUCTURE AND BIOLOGICAL-ACTIVITY OF HUMAN HOMOLOGS OF THE RAF MIL ONCOGENE [J].
BONNER, TI ;
KERBY, SB ;
SUTRAVE, P ;
GUNNELL, MA ;
MARK, G ;
RAPP, UR .
MOLECULAR AND CELLULAR BIOLOGY, 1985, 5 (06) :1400-1407
[5]   GENETIC AND CYTOGENETIC LOCALIZATION OF THE HOMEO BOX CONTAINING GENES ON MOUSE CHROMOSOME-6 AND HUMAN CHROMOSOME-7 [J].
BUCAN, M ;
YANGFENG, T ;
COLBERGPOLEY, AM ;
WOLGEMUTH, DJ ;
GUENET, JL ;
FRANCKE, U ;
LEHRACH, H .
EMBO JOURNAL, 1986, 5 (11) :2899-2905
[6]   SIMPLIFIED GENE NOMENCLATURE [J].
CHANDY, KG ;
DOUGLAS, J ;
GUTMAN, GA ;
JAN, L ;
JOHO, R ;
KACZMAREK, L ;
MCKINNON, D ;
NORTH, RA ;
NUMA, S ;
PHILIPSON, L ;
RIBERA, AB ;
RUDY, B ;
SALKOFF, L ;
SWANSON, R ;
STEINER, D ;
TANOUYE, M ;
TEMPEL, BL .
NATURE, 1991, 352 (6330) :26-26
[7]   NUCLEOTIDE-SEQUENCE OF MURINE TRIOSEPHOSPHATE ISOMERASE CDNA [J].
CHENG, J ;
MIELNICKI, LM ;
PRUITT, SC ;
MAQUAT, LE .
NUCLEIC ACIDS RESEARCH, 1990, 18 (14) :4261-4261
[8]   MOLECULAR-CLONING, CHARACTERIZATION, AND GENOMIC LOCALIZATION OF A HUMAN POTASSIUM CHANNEL GENE [J].
CURRAN, ME ;
LANDES, GM ;
KEATING, MT .
GENOMICS, 1992, 12 (04) :729-737
[9]   THE HUMAN MET ONCOGENE IS RELATED TO THE TYROSINE KINASE ONCOGENES [J].
DEAN, M ;
PARK, M ;
LEBEAU, MM ;
ROBINS, TS ;
DIAZ, MO ;
ROWLEY, JD ;
BLAIR, DG ;
VANDEWOUDE, GF .
NATURE, 1985, 318 (6044) :385-388
[10]  
DULEY J, 1974, GENETICS, V76, P93