Characterisation of expression of mDMAHP a homeodomain-encoding gene at the murine DM locus

被引:34
作者
Heath, SK
Carne, S
Hoyle, C
Johnson, KJ
Wells, DJ
机构
[1] CHARING CROSS & WESTMINSTER MED SCH,DEPT PHARMACOL,GENE TARGETING UNIT,LONDON W6 8RF,ENGLAND
[2] CHARING CROSS & WESTMINSTER MED SCH,DEPT CLIN NEUROSCI,GENE TARGETING UNIT,LONDON W6 8RF,ENGLAND
[3] UNIV GLASGOW,ANDERSON COLL,IBLS,DIV MOL GENET,GLASGOW G11 6NU,LANARK,SCOTLAND
基金
英国惠康基金;
关键词
D O I
10.1093/hmg/6.5.651
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
We examined the expression of the murine homologue of myotonic dystrophy associated homeodomain protein (mDMAHP) using two different strategies. The first approach, RT-PCR, detected spliced transcripts in a wide range of embryonic and adult tissues, in a pattern overlapping substantially with the expression of mDMPK. A second approach, the generation of transgenic mice expressing the lacZ reporter gene from a 4.3 kb promoter fragment, also demonstrated expression in a range of tissues with potential links to the phenotype in myotonic dystrophy. We conclude that murine DMAHP has a similar pattern of expression to human DMAHP and will serve as a useful model for functional studies of this gene, although species differences, such as the reduced CpG island (1.8 kb compared with 3.5 kb) must be carefully considered.
引用
收藏
页码:651 / 657
页数:7
相关论文
共 42 条
  • [1] NUMBER OF CPG ISLANDS AND GENES IN HUMAN AND MOUSE
    ANTEQUERA, F
    BIRD, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) : 11995 - 11999
  • [2] TISSUE-SPECIFIC EXPRESSION OF AN ALPHA-SKELETAL ACTIN LACZ FUSION GENE DURING DEVELOPMENT IN TRANSGENIC MICE
    ASANTE, EA
    BOSWELL, JM
    BURT, DW
    BULFIELD, G
    [J]. TRANSGENIC RESEARCH, 1994, 3 (01) : 59 - 66
  • [3] CLONING OF THE ESSENTIAL MYOTONIC-DYSTROPHY REGION AND MAPPING OF THE PUTATIVE DEFECT
    ASLANIDIS, C
    JANSEN, G
    AMEMIYA, C
    SHUTLER, G
    MAHADEVAN, M
    TSILFIDIS, C
    CHEN, C
    ALLEMAN, J
    WORMSKAMP, NGM
    VOOIJS, M
    BUXTON, J
    JOHNSON, K
    SMEETS, HJM
    LENNON, GG
    CARRANO, AV
    KORNELUK, RG
    WIERINGA, B
    DEJONG, PJ
    [J]. NATURE, 1992, 355 (6360) : 548 - 551
  • [4] AN EXONIC MUTATION IN THE HUP2 PAIRED DOMAIN GENE CAUSES WAARDENBURG SYNDROME
    BALDWIN, CT
    HOTH, CF
    AMOS, JA
    DASILVA, EO
    MILUNSKY, A
    [J]. NATURE, 1992, 355 (6361) : 637 - 638
  • [5] Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome
    Basson, CT
    Bachinsky, DR
    Lin, RC
    Levi, T
    Elkins, JA
    Soults, J
    Grayzel, D
    Kroumpouzou, E
    Traill, TA
    LeblancStraceski, J
    Renault, B
    Kucherlapati, R
    Seidman, JG
    Seidman, CE
    [J]. NATURE GENETICS, 1997, 15 (01) : 30 - 35
  • [6] MOLECULAR-BASIS OF MYOTONIC-DYSTROPHY - EXPANSION OF A TRINUCLEOTIDE (CTG) REPEAT AT THE 3' END OF A TRANSCRIPT ENCODING A PROTEIN-KINASE FAMILY MEMBER
    BROOK, JD
    MCCURRACH, ME
    HARLEY, HG
    BUCKLER, AJ
    CHURCH, D
    ABURATANI, H
    HUNTER, K
    STANTON, VP
    THIRION, JP
    HUDSON, T
    SOHN, R
    ZEMELMAN, B
    SNELL, RG
    RUNDLE, SA
    CROW, S
    DAVIES, J
    SHELBOURNE, P
    BUXTON, J
    JONES, C
    JUVONEN, V
    JOHNSON, K
    HARPER, PS
    SHAW, DJ
    HOUSMAN, DE
    [J]. CELL, 1992, 68 (04) : 799 - 808
  • [7] PRESYMPTOMATIC DIAGNOSIS OF MYOTONIC-DYSTROPHY
    BRUNNER, HG
    NILLESEN, W
    VANOOST, BA
    JANSEN, G
    WIERINGA, B
    ROPERS, HH
    SMEETS, HJM
    [J]. JOURNAL OF MEDICAL GENETICS, 1992, 29 (11) : 780 - 784
  • [8] DETECTION OF AN UNSTABLE FRAGMENT OF DNA SPECIFIC TO INDIVIDUALS WITH MYOTONIC-DYSTROPHY
    BUXTON, J
    SHELBOURNE, P
    DAVIES, J
    JONES, C
    VANTONGEREN, T
    ASLANIDIS, C
    DEJONG, P
    JANSEN, G
    ANVRET, M
    RILEY, B
    WILLIAMSON, R
    JOHNSON, K
    [J]. NATURE, 1992, 355 (6360) : 547 - 548
  • [9] ABSENCE OF MYOTONIC-DYSTROPHY PROTEIN-KINASE (DMPK) MESSENGER-RNA AS A RESULT OF A TRIPLET REPEAT EXPANSION IN MYOTONIC-DYSTROPHY
    CARANGO, P
    NOBLE, JE
    MARKS, HG
    FUNANAGE, VL
    [J]. GENOMICS, 1993, 18 (02) : 340 - 348
  • [10] AN UNSTABLE TRIPLET REPEAT IN A GENE RELATED TO MYOTONIC MUSCULAR-DYSTROPHY
    FU, YH
    PIZZUTI, A
    FENWICK, RG
    KING, J
    RAJNARAYAN, S
    DUNNE, PW
    DUBEL, J
    NASSER, GA
    ASHIZAWA, T
    DEJONG, P
    WIERINGA, B
    KORNELUK, R
    PERRYMAN, MB
    EPSTEIN, HF
    CASKEY, CT
    [J]. SCIENCE, 1992, 255 (5049) : 1256 - 1258