Primary defects in the lens underlie complex anterior segment abnormalities of the Pax6 heterozygous eye

被引:85
|
作者
Collinson, JM
Quinn, JC
Buchanan, MA
Kaufman, MH
Wedden, SE
West, JD
Hill, RE
机构
[1] Univ Edinburgh, Dept Reprod & Dev Sci, Edinburgh EH8 9XD, Midlothian, Scotland
[2] Univ Edinburgh, Dept Biomed Sci, Genes & Dev Grp, Edinburgh EH8 9XD, Midlothian, Scotland
[3] MRC, Comparat & Dev Genet Sect, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
关键词
D O I
10.1073/pnas.161144098
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
We describe lens defects in heterozygous small eye mice, and autonomous deficiencies of Pax6(+/-) cells in the developing lens of Pax6(+/+) <----> Pax6(+/-) chimeras. Two separate defects of the lens were identified by analyzing the distribution of heterozygous cells in chimeras: Pax6(+/-) cells are less readily incorporated into the lens placode than wild type, and those that are incorporated into the lens are not maintained efficiently in the proliferating lens epithelium. The lens of chimeric eyes is, therefore, predominantly wild type from embryonic day 16.5 onwards, whereas heterozygous cells contribute normally to all other eye tissues. Eye size and defects of the iris and cornea are corrected in fetal and adult chimeras with up to 80% mutant cells. Therefore, these aspects of the phenotype may be secondary consequences of primary defects in the lens, which has clinical relevance for the human aniridia (PAX6(+/-)) phenotype.
引用
收藏
页码:9688 / 9693
页数:6
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