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大鼠小眼症中Pax-6基因的突变与中脑嵴细胞迁移受损有关。

A mutation in the Pax-6 gene in rat small eye is associated with impaired migration of midbrain crest cells.

作者信息

Matsuo T, Osumi-Yamashita N, Noji S, Ohuchi H, Koyama E, Myokai F, Matsuo N, Taniguchi S, Doi H, Iseki S

机构信息

Department of Ophthalmology, Okayama University Medical School, Japan.

出版信息

Nat Genet. 1993 Apr;3(4):299-304. doi: 10.1038/ng0493-299.

Abstract

The rat small eye strain (rSey) lacks eyes and nose in the homozygote, and is similar to the mouse Sey strain with mutations in the Pax-6 gene. We isolated Pax-6 cDNA clones from an rSey homozygote library, and found an internal deletion of about 600 basepairs in the serine/threonine-rich domain. At the genomic level, a single base (G) insertion in an exon generates an abnormal 5' donor splice site, thereby producing the truncated mRNA. Anterior midbrain crest cells in the homozygous rSey embryos reached the eye rudiments but did not migrate any further to the nasal rudiments, suggesting that the Pax-6 gene is involved in conducting migration of neural crest cells from the anterior midbrain.

摘要

大鼠小眼品系(rSey)纯合子缺乏眼睛和鼻子,与Pax-6基因发生突变的小鼠Sey品系相似。我们从rSey纯合子文库中分离出Pax-6 cDNA克隆,发现在富含丝氨酸/苏氨酸的结构域中有一个约600个碱基对的内部缺失。在基因组水平上,一个外显子中的单个碱基(G)插入产生了异常的5'供体剪接位点,从而产生截短的mRNA。纯合rSey胚胎中的前脑嵴细胞到达眼原基,但没有进一步迁移到鼻原基,这表明Pax-6基因参与引导神经嵴细胞从前脑迁移。

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