Genes for cognitive function:: Developments on the X

被引:58
作者
Gécz, J [1 ]
Mulley, J
机构
[1] Womens & Childrens Hosp, Ctr Med Genet, Dept Cytogenet & Mol Genet, N Adelaide, SA 5006, Australia
[2] Univ Adelaide, Dept Genet, Adelaide, SA, Australia
[3] Univ Adelaide, Dept Pediat, Adelaide, SA, Australia
关键词
D O I
10.1101/gr.10.2.157
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
Developments in human genome research enabled the first steps toward a molecular understanding of cognitive function. That there are numerous genes on the X chromosome affecting intelligence at the lower end of the cognitive range is no longer in doubt. Naturally occurring mutations have so far led to the identification of seven genes accounting for a small proportion of familial nonspecific X-linked mental retardation. These new data indicate that normal expression of many more X-linked and autosomal genes contribute to cognitive function. The emerging knowledge implicating genes in intracellular signaling pathways provides the insight to identify as candidates other X-linked and autosomal genes regulating the normal development of cognitive function. Recent advances in unravelling the underlying molecular complexity have been spectacular but represent only the beginning, and new technologies will need to be introduced to complete the picture.
引用
收藏
页码:157 / 163
页数:7
相关论文
共 57 条
  • [1] PAK3 mutation in nonsyndromic X-linked mental retardation
    Allen, KM
    Gleeson, JG
    Bagrodia, S
    Partington, MW
    MacMillan, JC
    Cerione, RA
    Mulley, JC
    Walsh, CA
    [J]. NATURE GENETICS, 1998, 20 (01) : 25 - 30
  • [2] Mind the GAP, Rho, Rab and GDI
    Antonarakis, SE
    Van Aelst, L
    [J]. NATURE GENETICS, 1998, 19 (02) : 106 - 108
  • [3] LINKAGE ANALYSIS SUGGESTS AT LEAST 2 LOCI FOR X-LINKED NON-SPECIFIC MENTAL-RETARDATION
    ARVEILER, B
    ALEMBIK, Y
    HANAUER, A
    JACOBS, P
    TRANEBJAERG, L
    MIKKELSEN, M
    PUISSANT, H
    PIET, LL
    MANDEL, JL
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1988, 30 (1-2): : 473 - 483
  • [4] BAGRODIA S, 1995, J BIOL CHEM, V270, P27995
  • [5] Characterization of integrin-tetraspanin adhesion complexes: Role of tetraspanins in integrin signaling
    Berditchevski, F
    Odintsova, E
    [J]. JOURNAL OF CELL BIOLOGY, 1999, 146 (02) : 477 - 492
  • [6] Billuart P, 1998, PATHOL BIOL, V46, P678
  • [7] A SYNAPTIC MODEL OF MEMORY - LONG-TERM POTENTIATION IN THE HIPPOCAMPUS
    BLISS, TVP
    COLLINGRIDGE, GL
    [J]. NATURE, 1993, 361 (6407) : 31 - 39
  • [8] A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation
    Carrié, A
    Jun, L
    Bienvenu, T
    Vinet, MC
    McDonell, N
    Couvert, P
    Zemni, R
    Cardona, A
    Van Buggenhout, G
    Frints, S
    Hamel, B
    Moraine, C
    Ropers, HH
    Strom, T
    Howell, GR
    Whittaker, A
    Ross, MT
    Kahn, A
    Fryns, JP
    Beldjord, C
    Marynen, P
    Chelly, J
    [J]. NATURE GENETICS, 1999, 23 (01) : 25 - 31
  • [9] Breakthroughs in molecular and cellular mechanisms underlying X-linked mental retardation
    Chelly, J
    [J]. HUMAN MOLECULAR GENETICS, 1999, 8 (10) : 1833 - 1838
  • [10] Recurrence risks in mental retardation
    Crow, YJ
    Tolmie, JL
    [J]. JOURNAL OF MEDICAL GENETICS, 1998, 35 (03) : 177 - 182