Subfunctionalization of duplicated zebrafish pax6 genes by cis-regulatory divergence

被引:132
作者
Kleinjan, Dirk A. [1 ]
Bancewicz, Ruth M. [1 ]
Gautier, Philippe [1 ]
Dahm, Ralf [2 ]
Schonthaler, Helia B. [2 ]
Damante, Giuseppe [3 ]
Seawright, Anne [1 ]
Hever, Ann M. [1 ]
Yeyati, Patricia L. [1 ]
van Heyningen, Veronica [1 ]
Coutinho, Pedro [1 ]
机构
[1] Western Gen Hosp, MRC, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
[2] Max Planck Inst Dev Biol, Dept Genet, Tubingen, Germany
[3] Univ Udine, Dept Sci & Biomed Technol, I-33100 Udine, Italy
来源
PLOS GENETICS | 2008年 / 4卷 / 02期
基金
英国医学研究理事会;
关键词
D O I
10.1371/journal.pgen.0040029
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Gene duplication is a major driver of evolutionary divergence. In most vertebrates a single PAX6 gene encodes a transcription factor required for eye, brain, olfactory system, and pancreas development. In zebrafish, following a postulated whole-genome duplication event in an ancestral teleost, duplicates pax6a and pax6b jointly fulfill these roles. Mapping of the homozygously viable eye mutant sunrise identified a homeodomain missense change in pax6b, leading to loss of target binding. The mild phenotype emphasizes role-sharing between the co-orthologues. Meticulous mapping of isolated BACs identified perturbed synteny relationships around the duplicates. This highlights the functional conservation of pax6 downstream (3') control sequences, which in most vertebrates reside within the introns of a ubiquitously expressed neighbour gene, ELP4, whose pax6a-linked exons have been lost in zebrafish. Reporter transgenic studies in both mouse and zebrafish, combined with analysis of vertebrate sequence conservation, reveal loss and retention of specific cis-regulatory elements, correlating strongly with the diverged expression of co-orthologues, and providing clear evidence for evolution by subfunctionalization.
引用
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页数:14
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