A high-resolution genetic map around waltzer on mouse Chromosome 10 and identification of a new allele of waltzer

被引:22
作者
Bryda, EC [1 ]
Ling, H [1 ]
Flaherty, L [1 ]
机构
[1] NEW YORK STATE DEPT HLTH, WADSWORTH CTR, LAB DEV GENET, MOL GENET PROGRAM, ALBANY, NY 12201 USA
关键词
D O I
10.1007/s003359900336
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
A new autosomal recessive mouse mutation characterized by deafness and circling behavior was recovered during mutagenesis experiments with chlorambucil (CHL). On the basis of allelism tests and linkage analyses, this mutation appears to represent a new allele of waltzer (v) that maps to mouse Chromosome (Chr) 10. We have designated this new allele, Albany waltzer (v(Alb)). A high-resolution map of the region around v was constructed from data from two intersubspecific backcrosses involving Mus musculus castaneus. The analysis of 648 backcross mice has allowed v(Alb) to be localized 1.1 +/- 0.4 cM distal to D10Mit60 and 0.2 +/- 0.2 cM proximal to a cluster of four markers, D10Mit172, D10Mit112, D10Mit48, and D10Mit196. An independent backcross was used to confirm the map order and distances in the v(Alb) backcross. The two linkage maps were consistent, indicating that the lesion in v(Alb), which is presumed to be a deletion based on the known action of CHL, is small and has not significantly altered the map at this level of detection. Additionally, three genes (Ros1, Grik2 and Zfa) were eliminated as possible candidates for v(Alb), and several SSLP markers were separated genetically.
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页码:1 / 4
页数:4
相关论文
共 29 条
[1]   THE MOUSE SNELLS WALTZER DEAFNESS GENE ENCODES AN UNCONVENTIONAL MYOSIN REQUIRED FOR STRUCTURAL INTEGRITY OF INNER-EAR HAIR-CELLS [J].
AVRAHAM, KB ;
HASSON, T ;
STEEL, KP ;
KINGSLEY, DM ;
RUSSELL, LB ;
MOOSEKER, MS ;
COPELAND, NG ;
JENKINS, NA .
NATURE GENETICS, 1995, 11 (04) :369-375
[2]   TOWARDS HIGH-RESOLUTION MAPS OF THE MOUSE AND HUMAN GENOMES - A FACILITY FOR ORDERING MARKERS TO 0.1 CM RESOLUTION [J].
BREEN, M ;
DEAKIN, L ;
MACDONALD, B ;
MILLER, S ;
SIBSON, R ;
TARTTELIN, E ;
AVNER, P ;
BOURGADE, F ;
GUENET, JL ;
MONTAGUTELLI, X ;
POIRIER, C ;
SIMON, D ;
TAILOR, D ;
BISHOP, M ;
KELLY, M ;
RYSAVY, F ;
RASTAN, S ;
NORRIS, D ;
SHEPHERD, D ;
ABBOTT, C ;
PILZ, A ;
HODGE, S ;
JACKSON, I ;
BOYD, Y ;
BLAIR, H ;
MASLEN, G ;
TODD, JA ;
REED, PW ;
STOYE, J ;
ASHWORTH, A ;
MCCARTHY, L ;
COX, R ;
SCHALKWYK, L ;
LEHRACH, H ;
KLOSE, J ;
GANGADHARAN, U ;
BROWN, S .
HUMAN MOLECULAR GENETICS, 1994, 3 (04) :621-627
[3]  
CANTANI A, 1989, Paediatrie und Paedologie, V24, P321
[4]  
CHAPDELAINE P, 1993, BIOTECHNIQUES, V14, P163
[5]   A GENETIC-LINKAGE MAP OF THE MOUSE - CURRENT APPLICATIONS AND FUTURE-PROSPECTS [J].
COPELAND, NG ;
JENKINS, NA ;
GILBERT, DJ ;
EPPIG, JT ;
MALTAIS, LJ ;
MILLER, JC ;
DIETRICH, WF ;
WEAVER, A ;
LINCOLN, SE ;
STEEN, RG ;
STEIN, LD ;
NADEAU, JH ;
LANDER, ES .
SCIENCE, 1993, 262 (5130) :57-66
[6]  
Deol M S, 1968, J Med Genet, V5, P137, DOI 10.1136/jmg.5.2.137
[7]   THE ANATOMY AND DEVELOPMENT OF THE MUTANTS PIROUETTE, SHAKER-1 AND WALTZER IN THE MOUSE [J].
DEOL, MS .
PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1956, 145 (919) :206-+
[8]  
DIETRICH W, 1992, GENETICS, V131, P423
[9]   A GENETIC-MAP OF THE MOUSE WITH 4,006 SIMPLE SEQUENCE LENGTH POLYMORPHISMS [J].
DIETRICH, WF ;
MILLER, JC ;
STEEN, RG ;
MERCHANT, M ;
DAMRON, D ;
NAHF, R ;
GROSS, A ;
JOYCE, DC ;
WESSEL, M ;
DREDGE, RD ;
MARQUIS, A ;
STEIN, LD ;
GOODMAN, N ;
PAGE, DC ;
LANDER, ES .
NATURE GENETICS, 1994, 7 (02) :220-245
[10]   A comprehensive genetic map of the mouse genome [J].
Dietrich, WF ;
Miller, J ;
Steen, R ;
Merchant, MA ;
DamronBoles, D ;
Husain, Z ;
Dredge, R ;
Daly, MJ ;
Ingalls, KA ;
OConnor, TJ ;
Evans, CA ;
DeAngelis, MM ;
Levinson, DM ;
Kruglyak, L ;
Goodman, N ;
Copeland, NG ;
Jenkins, NA ;
Hawkins, TL ;
Stein, L ;
Page, DC ;
Lander, ES .
NATURE, 1996, 380 (6570) :149-152