NOVEL TRIPLET REPEAT CONTAINING GENES IN HUMAN BRAIN - CLONING, EXPRESSION, AND LENGTH POLYMORPHISMS

被引:196
作者
LI, SH
MCINNIS, MG
MARGOLIS, RL
ANTONARAKIS, SE
ROSS, CA
机构
[1] JOHNS HOPKINS UNIV,SCH MED,DEPT PSYCHIAT,MOLEC NEUROBIOL LAB,ROSS 618,720 RUTLAND AVE,BALTIMORE,MD 21205
[2] JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROSCI,BALTIMORE,MD 21205
[3] JOHNS HOPKINS UNIV,SCH MED,CTR MED GENET,BALTIMORE,MD 21287
[4] JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT & MED,BALTIMORE,MD 21287
关键词
D O I
10.1006/geno.1993.1232
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
Human genes containing triplet repeats may markedly expand in length and cause neuropsychiatric disease, explaining the phenomenon of anticipation (increasing severity or earlier age of onset in successive generations in a pedigree). To identify novel genes with triplet repeats, we screened a human brain cDNA library with oligonucleotide probes containing CTG or CCG triplet repeats. Fourteen of 40 clones encoded novel human genes, and 8 of these inserts have been sequenced on both strands. All contain repeats, and 5 of the 8 have 9 or more consecutive perfect repeats. All are expressed in brain. Chromosomal assignments reveal a distribution of these genes on multiple autosomes and the X-chromosome. Further, the repeat length in two of the genes is highly polymorphic, making them valuable index linkage markers. We predict that many triplet repeat-containing genes exist; screening with the CTG probe suggests approximately 50-100 genes containing this type of repeat are expressed in the human brain. Since additional disorders, such as Huntington's disease, bipolar affective disorder, and possibly others, show features of anticipation, we suggest that these novel human genes with triplet repeats are candidates for causing neuropsychiatric diseases. © 1993 Academic Press. All rights reserved.
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收藏
页码:572 / 579
页数:8
相关论文
共 53 条
  • [1] BARON M, 1985, AM J PSYCHIAT, V142, P447
  • [2] SURVEY OF HUMAN AND RAT MICROSATELLITES
    BECKMANN, JS
    WEBER, JL
    [J]. GENOMICS, 1992, 12 (04) : 627 - 631
  • [3] BROOK JD, 1992, CELL, V69, P784
  • [4] TRIPLET REPEAT MUTATIONS IN HUMAN-DISEASE
    CASKEY, CT
    PIZZUTI, A
    FU, YH
    FENWICK, RG
    NELSON, DL
    [J]. SCIENCE, 1992, 256 (5058) : 784 - 789
  • [5] CLONING AND SEQUENCING OF A FULL LENGTH CDNA CODING FOR A HUMAN APOFERRITIN H-CHAIN - EVIDENCE FOR A MULTIGENE FAMILY
    COSTANZO, F
    SANTORO, C
    COLANTUONI, V
    BENSI, G
    RAUGEI, G
    ROMANO, V
    CORTESE, R
    [J]. EMBO JOURNAL, 1984, 3 (01) : 23 - 27
  • [6] ANALYSIS OF SP1 INVIVO REVEALS MULTIPLE TRANSCRIPTIONAL DOMAINS, INCLUDING A NOVEL GLUTAMINE-RICH ACTIVATION MOTIF
    COUREY, AJ
    TJIAN, R
    [J]. CELL, 1988, 55 (05) : 887 - 898
  • [7] PROGRAM DESCRIPTION - CENTER-DETUDE-DU-POLYMORPHISME-HUMAIN (CEPH) - COLLABORATIVE GENETIC-MAPPING OF THE HUMAN GENOME
    DAUSSET, J
    CANN, H
    COHEN, D
    LATHROP, M
    LALOUEL, JM
    WHITE, R
    [J]. GENOMICS, 1990, 6 (03) : 575 - 577
  • [8] HUMAN-GENETICS - THE COSTS OF INSTABILITY
    DAVIES, KE
    [J]. NATURE, 1992, 356 (6364) : 15 - 15
  • [9] Davis L, 1986, BASIC METHODS MOL BI
  • [10] Depaulo J. R. Jr., 1992, American Journal of Human Genetics, V51, pA44