Cooperation of Hoxa5 and Pax1 genes during formation of the pectoral girdle

被引:31
作者
Aubin, J [1 ]
Lemieux, M [1 ]
Moreau, J [1 ]
Lapointe, J [1 ]
Jeannotte, L [1 ]
机构
[1] Univ Laval, Ctr Hosp Univ Quebec, Ctr Rech Cancerol, Hotel Dieu Quebec, Quebec City, PQ G1R 2J6, Canada
基金
英国医学研究理事会;
关键词
Hox genes; Pax1; gene; pectoral girdle formation; chondrogenesis;
D O I
10.1006/dbio.2002.0596
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Hox and Pax transcription factors are master regulators of skeletal and organ morphogenesis. Some skeletal malformations encountered in Hoxa5 mutants are shared by the undulated (un) mice, which bear a point mutation in the Pax1 gene. To investigate whether Hoxa5 and Pax1 act in common pathways during skeletal development, we analyzed Hoxa5;un compound mutants. Our genetic studies show that Hoxa5 and Pax1 cooperate in the vertebral patterning of the cervicothoracic transition region and in acromion morphogenesis. The dynamics of expression of Hoxa5 and Pax1 in the pectoral girdle region suggest that both genes function in a complementary fashion during acromion formation. Whereas Pax1 is required for the recruitment of acromion precursor cells, Hoxa5 may provide regional cues essential for the correct formation of the acromion by ensuring Pax1 expression at the proper time and position during morphogenesis of the pectoral girdle. Hoxa5 also has a distinctive role in specifying the fate of perichondrial and chondrogenic cell lineages in a Sox9-dependent way. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:96 / 113
页数:18
相关论文
共 71 条
  • [1] Hox genes:: From master genes to micromanagers
    Akam, M
    [J]. CURRENT BIOLOGY, 1998, 8 (19) : R676 - R678
  • [2] Early postnatal lethality in Hoxa-5 mutant mice is attributable to respiratory tract defects
    Aubin, J
    Lemieux, M
    Tremblay, M
    Bérard, J
    Jeannotte, L
    [J]. DEVELOPMENTAL BIOLOGY, 1997, 192 (02) : 432 - 445
  • [3] Aubin J, 1998, DEV DYNAM, V212, P141, DOI 10.1002/(SICI)1097-0177(199805)212:1<141::AID-AJA13>3.0.CO
  • [4] 2-A
  • [5] UNDULATED, A MUTATION AFFECTING THE DEVELOPMENT OF THE MOUSE SKELETON, HAS A POINT MUTATION IN THE PAIRED BOX OF PAX-1
    BALLING, R
    DEUTSCH, U
    GRUSS, P
    [J]. CELL, 1988, 55 (03) : 531 - 535
  • [6] SOX9 directly regulates the type-II collagen gene
    Bell, DM
    Leung, KKH
    Wheatley, SC
    Ng, LJ
    Zhou, S
    Ling, KW
    Sham, MH
    Koopman, P
    Tam, PPL
    Cheah, KSE
    [J]. NATURE GENETICS, 1997, 16 (02) : 174 - 178
  • [7] Sox9 is required for cartilage formation
    Bi, WM
    Deng, JM
    Zhang, ZP
    Behringer, RR
    de Crombrugghe, B
    [J]. NATURE GENETICS, 1999, 22 (01) : 85 - 89
  • [8] The mouse Hoxd13spdh mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes
    Bruneau, S
    Johnson, KR
    Yamamoto, M
    Kuroiwa, A
    Duboule, D
    [J]. DEVELOPMENTAL BIOLOGY, 2001, 237 (02) : 345 - 353
  • [9] BURKE AC, 1995, DEVELOPMENT, V121, P333
  • [10] Carpenter EM, 1997, DEVELOPMENT, V124, P4505