Circling, deafness, and yellow coat displayed by yellow submarine (Ysb) and light coat and circling (Lcc) mice with mutations on chromosome 3

被引:17
作者
Dong, S
Leung, KKH
Pelling, AL
Lee, PYT
Tang, ASP
Heng, HHQ
Tsui, LC
Tease, C
Fisher, G
Steel, KP
Cheah, KSE
机构
[1] Univ Hong Kong, Dept Biochem, Hong Kong, Hong Kong, Peoples R China
[2] Univ Toronto, Hosp Sick Children, Dept Genet & Genom Biol, Toronto, ON M5G 1X8, Canada
[3] MRC, Mammalian Genet Unit, Didcot OX11 ORD, Oxon, England
[4] MRC, Inst Hearing Res, Nottingham NG7 2RD, England
基金
英国医学研究理事会;
关键词
mouse; hair; pigmentation; ear; deaf; transgenic; X-irradiation; chromosome; 3;
D O I
10.1006/geno.2002.6783
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
We describe here two mouse mutants, yellow submarine (Ysb) and light coat and circling (Lcc). Ysb arose as the result of insertions of a transgene, pAA2, into the genome. Lcc is an independent, radiation-induced mutation. Both mutants are characterized by recessive circling behavior and deafness, associated with a non-segregating, semi-dominant yellow coat color. Complementation tests showed that Ysb and Lcc are allelic. We attribute the yellow coat in Ysb and Lcc mice to the absence of black awl overhairs, increased agouti zigzag underhairs, and the presence of agouti awls with long subapical yellow pigment. Chromosomal mapping and genomic characterization showed the Ysb and Lcc mutations involve complex chromosomal rearrangements in overlapping regions of mouse chromosome 3, A2/A3-B/C and B-E1, respectively. Ysb and Lcc show for the first time, to our knowledge, the presence of genes in the B-C region of chromosome 3 important for balance and hearing and the pigmentation and specification of coat hair.
引用
收藏
页码:777 / 784
页数:8
相关论文
共 42 条
[1]  
[Anonymous], 1979, COAT COLORS MICE MOD
[2]   The genetics of pigmentation: From fancy genes to complex traits [J].
Barsh, GS .
TRENDS IN GENETICS, 1996, 12 (08) :299-305
[3]  
BEECHEY CV, 1996, GENETIC VARIANTS STR
[4]   NEW FAMILIAL SYNDROME WITH ATAXIA, HEARING-LOSS, AND MENTAL-RETARDATION - REPORT OF 3 BROTHERS [J].
BERMAN, W ;
HASLAM, RHA ;
KONIGSMA.BW ;
CAPUTE, AJ ;
MIGEON, CJ .
ARCHIVES OF NEUROLOGY, 1973, 29 (04) :258-261
[5]   SHOT, a SHOX-related homeobox gene, is implicated in craniofacial, brain, heart, and limb development [J].
Blaschke, RJ ;
Monaghan, AP ;
Schiller, S ;
Schechinger, B ;
Rao, E ;
Padilla-Nash, H ;
Ried, T ;
Rappold, GA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (05) :2406-2411
[6]  
CARTER TC, 1954, J HERED, V45, P150
[7]   HUMAN COL2A1-DIRECTED SV40 T-ANTIGEN EXPRESSION IN TRANSGENIC AND CHIMERIC MICE RESULTS IN ABNORMAL SKELETAL DEVELOPMENT [J].
CHEAH, KSE ;
LEVY, A ;
TRAINOR, PA ;
WAI, AWK ;
KUFFNER, T ;
SO, CL ;
LEUNG, KKH ;
LOVELLBADGE, RH ;
TAM, PPL .
JOURNAL OF CELL BIOLOGY, 1995, 128 (1-2) :223-237
[8]   Mapping of the IDDM locus Idd3 to a 0.35-cM interval containing the interleukin-2 gene [J].
Denny, P ;
Lord, CJ ;
Hill, NJ ;
Goy, JV ;
Levy, ER ;
Podolin, PL ;
Peterson, LB ;
Wicker, LS ;
Todd, JA ;
Lyons, PA .
DIABETES, 1997, 46 (04) :695-700
[9]   The coat of the mouse (Mus musculus) [J].
Dry, FW .
JOURNAL OF GENETICS, 1926, 16 (03) :287-340
[10]  
EVANS E P, 1987, P93