A genetic blueprint for cardiac development

被引:469
作者
Srivastava, D
Olson, EN
机构
[1] Univ Texas, SW Med Ctr, Dept Mol Biol, Dallas, TX 75390 USA
[2] Univ Texas, SW Med Ctr, Dept Pediat, Dallas, TX 75390 USA
关键词
D O I
10.1038/35025190
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Congenital heart disease is the leading non-infectious cause of death in children. It is becoming increasingly clear that many cardiac abnormalities once thought to have multifactorial aetiologies are attributable to mutations in developmental control genes. The consequences of these mutations can be manifest at birth as life-threatening cardiac malformations or later as more subtle cardiac abnormalities. Understanding the genetic underpinnings of cardiac development has important implications not only for understanding congenital heart disease, but also for the possibility of cardiac repair through genetic reprogramming of non-cardiac cells to a cardiogenic fate.
引用
收藏
页码:221 / 226
页数:6
相关论文
共 53 条
  • [1] Regulation of chamber-specific gene expression in the developing heart by Irx4
    Bao, ZZ
    Bruneau, BG
    Seidman, JG
    Seidman, CE
    Cepko, CL
    [J]. SCIENCE, 1999, 283 (5405) : 1161 - 1164
  • [2] Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations
    Basson, CT
    Huang, TS
    Lin, RC
    Bachinsky, DR
    Weremowicz, S
    Vaglio, A
    Bruzzone, R
    Quadrelli, R
    Lerone, M
    Romeo, G
    Silengo, M
    Pereira, A
    Krieger, J
    Mesquita, SF
    Kamisago, M
    Morton, CC
    Pierpont, MEM
    Müller, CW
    Seidman, JG
    Seidman, CE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (06) : 2919 - 2924
  • [3] 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
  • [4] Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways
    Benson, DW
    Silberbach, GM
    Kavanaugh-McHugh, A
    Cottrill, C
    Zhang, YZ
    Riggs, S
    Smalls, O
    Johnson, MC
    Watson, MS
    Seidman, JG
    Seidman, CE
    Plowden, J
    Kugler, JD
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (11) : 1567 - 1573
  • [5] Homeodomain factor Nkx2-5 controls left/right asymmetric expression of bHLH gene eHand during murine heart development
    Biben, C
    Harvey, RP
    [J]. GENES & DEVELOPMENT, 1997, 11 (11) : 1357 - 1369
  • [6] Requirement of type III TGF-β receptor for endocardial cell transformation in the heart
    Brown, CB
    Boyer, AS
    Runyan, RB
    Barnett, JV
    [J]. SCIENCE, 1999, 283 (5410) : 2080 - 2082
  • [7] Cardiac expression of the ventricle-specific homeobox gene Irx4 is modulated by Nkx2-5 and dHand
    Bruneau, BG
    Bao, ZZ
    Tanaka, M
    Schott, JJ
    Izumo, S
    Cepko, CL
    Seidman, JG
    Seidman, CE
    [J]. DEVELOPMENTAL BIOLOGY, 2000, 217 (02) : 266 - 277
  • [8] Mechanisms of left-right determination in vertebrates
    Capdevila, J
    Vogan, KJ
    Tabin, CJ
    Belmonte, JCI
    [J]. CELL, 2000, 101 (01) : 9 - 21
  • [9] Abnormal blood vessel development and lethality in embryos lacking a single VEGF allele
    Carmeliet, P
    Ferreira, V
    Breier, G
    Pollefeyt, S
    Kieckens, L
    Gertsenstein, M
    Fahrig, M
    Vandenhoeck, A
    Harpal, K
    Eberhardt, C
    Declercq, C
    Pawling, J
    Moons, L
    Collen, D
    Risau, W
    Nagy, A
    [J]. NATURE, 1996, 380 (6573) : 435 - 439
  • [10] Clouthier DE, 1998, DEVELOPMENT, V125, P813