The PAX258 Gene Subfamily: A Comparative Perspective

被引:30
作者
Goode, Debbie K. [1 ,2 ]
Elgar, Greg [1 ]
机构
[1] Univ London, Sch Biol & Chem Sci, London E1 4NS, England
[2] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge, England
基金
英国医学研究理事会;
关键词
PAX2; PAX5; PAX8; whole genome duplication; functional redundancy; cis-regulatory elements; midbrain-hindbrain boundary; inner ear; choroid fissure; spinal cord; kidney; MIDBRAIN-HINDBRAIN BOUNDARY; RENAL-COLOBOMA SYNDROME; DORSAL SPINAL-CORD; PAIRED BOX GENE; CONSERVED NONCODING SEQUENCES; DEVELOPING EXCRETORY SYSTEM; TRANSCRIPTION FACTOR GENES; OTIC PLACODE INDUCTION; CENTRAL-NERVOUS-SYSTEM; B-CELL IDENTITY;
D O I
10.1002/dvdy.22146
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Whole genome duplication events are thought to have substantially contributed to organismal complexity, largely via divergent transcriptional regulation. Members of the vertebrate PAX2, PAX5 and PAX8 gene subfamily derived from an ancient class of paired box genes and arose from such whole genome duplication events. These genes are critical in establishing the midbrain-hindbrain boundary, specifying interneuron populations anti for eye, ear and kidney development. Also PAX2 has adopted a unique role in pancreas development, whilst PAX5 is essential for early B-cell differentiation. The contribution of PAX258 genes to their collective role has diverged across paralogues and the animal lineages, resulting in a complex wealth of literature. It is now timely to provide a comprehensive comparative overview of these genes and their ancient and divergent roles. We also discuss their fundamental place within gene regulatory networks and the likely influence of cis-regulatory elements over their differential roles during early animal development. Developmental Dynamics 238:2951-2974, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:2951 / 2974
页数:24
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