Pax genes: regulators of lineage specification and progenitor cell maintenance

被引:150
作者
Blake, Judith A. [1 ]
Ziman, Melanie R. [1 ]
机构
[1] Edith Cowan Univ, Sch Med Sci, Joondalup, WA 6027, Australia
来源
DEVELOPMENT | 2014年 / 141卷 / 04期
关键词
Pax genes; Embryogenesis; Lineage determination; RENAL-COLOBOMA SYNDROME; PAIRED BOX GENE; SYNDROME TYPE-I; CARDIAC NEURAL CREST; CEREBELLAR-ATAXIA; MISSENSE MUTATION; STEM-CELLS; CONGENITAL HYPOTHYROIDISM; GILLESPIE-SYNDROME; SKELETAL-MUSCLE;
D O I
10.1242/dev.091785
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Pax genes encode a family of transcription factors that orchestrate complex processes of lineage determination in the developing embryo. Their key role is to specify and maintain progenitor cells through use of complex molecular mechanisms such as alternate RNA splice forms and gene activation or inhibition in conjunction with protein co-factors. The significance of Pax genes in development is highlighted by abnormalities that arise from the expression of mutant Pax genes. Here, we review the molecular functions of Pax genes during development and detail the regulatory mechanisms by which they specify and maintain progenitor cells across various tissue lineages. We also discuss mechanistic insights into the roles of Pax genes in regeneration and in adult diseases, including cancer.
引用
收藏
页码:737 / 751
页数:15
相关论文
共 232 条
[1]  
ACAMPORA D, 1995, DEVELOPMENT, V121, P3279
[2]   Glial versus melanocyte cell fate choice: Schwann cell precursors as a cellular origin of melanocytes [J].
Adameyko, Igor ;
Lallemend, Francois .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2010, 67 (18) :3037-3055
[3]   Schwann Cell Precursors from Nerve Innervation Are a Cellular Origin of Melanocytes in Skin [J].
Adameyko, Igor ;
Lallemend, Francois ;
Aquino, Jorge B. ;
Pereira, Jorge A. ;
Topilko, Piotr ;
Mueller, Thomas ;
Fritz, Nicolas ;
Beljajeva, Anna ;
Mochii, Makoto ;
Liste, Isabel ;
Usoskin, Dmitry ;
Suter, Ueli ;
Birchmeier, Carmen ;
Ernfors, Patrik .
CELL, 2009, 139 (02) :366-379
[4]   The scoliosis (sco)mouse:: a new allele of Pax1 [J].
Adham, IM ;
Gille, M ;
Gamel, AJ ;
Reis, A ;
Dressel, R ;
Steding, G ;
Brand-Saberi, B ;
Engel, W .
CYTOGENETIC AND GENOME RESEARCH, 2005, 111 (01) :16-26
[5]   Genetic and physical interaction of Meis2, Pax3 and Pax7 during dorsal midbrain development [J].
Agoston, Zsuzsa ;
Li, Naixin ;
Haslinger, Anja ;
Wizenmann, Andrea ;
Schulte, Dorothea .
BMC DEVELOPMENTAL BIOLOGY, 2012, 12
[6]   Meis2 competes with the Groucho co-repressor Tle4 for binding to Otx2 and specifies tectal fate without induction of a secondary midbrain-hindbrain boundary organizer [J].
Agoston, Zsuzsa ;
Schulte, Dorothea .
DEVELOPMENT, 2009, 136 (19) :3311-3322
[7]   PAX2 mutations in renal-coloboma syndrome:: mutational hotspot and germline mosaicism [J].
Amiel, J ;
Audollent, S ;
Joly, D ;
Dureau, P ;
Salomon, R ;
Tellier, AL ;
Augé, J ;
Bouissou, F ;
Antignac, C ;
Gubler, MC ;
Eccles, MR ;
Munnich, A ;
Vekemans, M ;
Lyonnet, S ;
Attié-Bitach, T .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2000, 8 (11) :820-826
[8]   The role of Pax6 in regulating the orientation and mode of cell division of progenitors in the mouse cerebral cortex [J].
Asami, Maki ;
Pilz, Gregor A. ;
Ninkovic, Jovica ;
Godinho, Leanne ;
Schroeder, Timm ;
Huttner, Wieland B. ;
Goetz, Magdalena .
DEVELOPMENT, 2011, 138 (23) :5067-5078
[9]  
Asher JH, 1996, HUM MUTAT, V7, P30, DOI 10.1002/(SICI)1098-1004(1996)7:1<30::AID-HUMU4>3.0.CO
[10]  
2-T