GENETIC-MAP OF 12 POLYMORPHIC LOCI ON RAT CHROMOSOME-1

被引:26
作者
GOLDMUNTZ, EA
REMMERS, EF
ZHA, HB
CASH, JM
MATHERN, P
CROFFORD, LJ
WILDER, RL
机构
[1] Arthritis and Rheumatism Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda
关键词
D O I
10.1006/geno.1993.1261
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
Twelve polymorphic markers identified by restriction fragment length polymorphism (RFLP) analysis or simple sequence repeat (SSR) polymorphism analysis were assigned to rat chromosome 1 by linkage analysis of F2 intercross progeny of F344/N and LEW/N inbred rat strains. One linkage group, covering 46.3 cM, consisted of eight markers including five genes, TNT (fast skeletal troponin T), IGF2 (insulin-like growth factor 2), MYL2 (MLC2 gene for muscle myosin light chain 2), ALDOA (aldolase A), and HBB (hemoglobin β-chain); one anonymous locus, D1N64; one marker related to the carboxypeptidase B gene, CARBO7 -related sequence; and one marker related to the parathyroid hormone gene, PTH-related sequence. A second linkage group, covering 45.0 cM, consisted of three markers including two anonymous loci, 2B1 and D1N40, and one gene, TCP1 (T-complex 1). INS1 (insulin 1), which has been previously assigned to rat chromosome 1, was not linked to these markers. The SSR markers were highly polymorphic in 13 inbred rat strains (SHR/N, WKY/N, MNR/N, MR/N, LOU/MN, BN/SsN, BUF/N, WBB1/N, WBB2/N, AC1/N, LER/N, F344/N, and LEW/N). These markers, located on chromosome 1, will be useful in genetic studies in rats. © 1993 Academic Press. All rights reserved.
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页码:761 / 764
页数:4
相关论文
共 17 条
  • [1] REPORT OF THE COMPARATIVE COMMITTEE FOR HUMAN, MOUSE AND OTHER RODENTS
    DAVISSON, MT
    LALLEY, PA
    PETERS, J
    DOOLITTLE, DP
    HILLYARD, AL
    SEARLE, AG
    [J]. CYTOGENETICS AND CELL GENETICS, 1991, 58 (3-4): : 1152 - 1189
  • [2] DOOLITTLE DP, 1992, GENOMIC DATABASE MOU
  • [3] MOUSE CHROMOSOME-6
    ELLIOTT, RW
    MOORE, KJ
    [J]. MAMMALIAN GENOME, 1992, 3 : S81 - S103
  • [4] THE MOUSE PINK-EYED DILUTION GENE - ASSOCIATION WITH HUMAN PRADER-WILLI AND ANGELMAN SYNDROMES
    GARDNER, JM
    NAKATSU, Y
    GONDO, Y
    LEE, S
    LYON, MF
    KING, RA
    BRILLIANT, MH
    [J]. SCIENCE, 1992, 257 (5073) : 1121 - 1124
  • [5] HEDRICH HJ, 1990, GENETIC MONITORING I, P289
  • [6] CHROMOSOMAL MAPPING OF 2 GENETIC-LOCI ASSOCIATED WITH BLOOD-PRESSURE REGULATION IN HEREDITARY HYPERTENSIVE RATS
    HILBERT, P
    LINDPAINTNER, K
    BECKMANN, JS
    SERIKAWA, T
    SOUBRIER, F
    DUBAY, C
    CARTWRIGHT, P
    DEGOUYON, B
    JULIER, C
    TAKAHASI, S
    VINCENT, M
    GANTEN, D
    GEORGES, M
    LATHROP, GM
    [J]. NATURE, 1991, 353 (6344) : 521 - 529
  • [7] GENETIC-MAPPING OF A GENE CAUSING HYPERTENSION IN THE STROKE-PRONE SPONTANEOUSLY HYPERTENSIVE RAT
    JACOB, HJ
    LINDPAINTNER, K
    LINCOLN, SE
    KUSUMI, K
    BUNKER, RK
    MAO, YP
    GANTEN, D
    DZAU, VJ
    LANDER, ES
    [J]. CELL, 1991, 67 (01) : 213 - 224
  • [8] LANDER E S, 1987, Genomics, V1, P174, DOI 10.1016/0888-7543(87)90010-3
  • [9] THE GENE MAP OF THE NORWAY RAT (RATTUS-NORVEGICUS) AND COMPARATIVE MAPPING WITH MOUSE AND MAN
    LEVAN, G
    SZPIRER, J
    SZPIRER, C
    KLINGA, K
    HANSON, C
    ISLAM, MQ
    [J]. GENOMICS, 1991, 10 (03) : 699 - 718
  • [10] THE 1991 CATALOG OF MAPPED GENES AND REPORT OF THE NOMENCLATURE-COMMITTEE
    MCALPINE, PJ
    SHOWS, TB
    BOUCHEIX, C
    HUEBNER, M
    ANDERSON, WA
    [J]. CYTOGENETICS AND CELL GENETICS, 1991, 58 (1-2): : 5 - 102