基因分析表明,转录因子AP - 2α和Pax6在晶状体的正常模式形成和形态发生过程中相互协作。

Genetic analysis indicates that transcription factors AP-2alpha and Pax6 cooperate in the normal patterning and morphogenesis of the lens.

作者信息

Makhani Leila F, Williams Trevor, West-Mays Judith A

机构信息

Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.

出版信息

Mol Vis. 2007 Jul 19;13:1215-25.

DOI:
Abstract

PURPOSE

The similar lens phenotypes observed in mice with mutations in the genes encoding either Pax6 or AP-2alpha suggested that these transcription factors work together to regulate specific signaling cascades during lens development. In this study we examined the overlapping expression patterns of Pax6 and AP-2alpha in the developing mouse lens and further investigated their potential cooperative roles through the creation of double heterozygote mice.

METHODS

Colocalization of Pax6 and AP-2alpha expression patterns were performed on sections of mouse embryos at embryonic days 9.5, 10.5, 13.5, and 16 as well as on adult sections using immunofluorescence. To test the potential cooperation between these two transcription factors, two mouse strains heterozygous for the genes encoding either Pax6 or AP-2alpha were bred together to produce double heterozygous Pax6(+/lacZ)/AP-2alpha(+/-) mice. Histological examination was then performed on both embryonic and post-natal sections in order to compare double heterozygous Pax6(+/lacZ)/AP-2alpha(+/-) eyes to single heterozygote and wildtype eyes.

RESULTS

Examination of the developmental stages showed distinct colocalization of Pax6 and AP-2alpha protein in the anterior lens epithelium. However, Pax6 expression continued further into the transitional zone of the lens whereas AP-2alpha expression ceased just prior to the region where epithelial cells differentiate into fiber cells. Histological investigation of embryonic and post-natal mutant mouse eyes showed that while single Pax6 heterozygote mice exhibited remnants of a corneal-lenticular adhesion, the lens and cornea were physically separated. In contrast, the Pax6(+/lacZ)/AP-2alpha(+/-) double heterozygotes displayed a distinct lens stalk, which protruded towards the surface of the cornea, creating a direct corneal-lenticular attachment.

CONCLUSIONS

Colocalization of Pax6 and AP-2alpha was mainly observed in the proliferating central lens epithelium, the same region in which the lens stalk phenotype was observed in the double heterozygous Pax6(+/lacZ)/AP-2alpha(+/-) eyes. The more severe phenotype observed in these double heterozygous mice, as compared to the single heterozygotes, suggests that Pax6 and AP-2alpha may work synergistically to control lens development.

摘要

目的

在编码Pax6或AP - 2α的基因发生突变的小鼠中观察到相似的晶状体表型,这表明这些转录因子在晶状体发育过程中共同作用以调节特定的信号级联反应。在本研究中,我们检测了Pax6和AP - 2α在发育中的小鼠晶状体中的重叠表达模式,并通过创建双杂合子小鼠进一步研究了它们潜在的协同作用。

方法

使用免疫荧光法对胚胎第9.5、10.5、13.5和16天的小鼠胚胎切片以及成年小鼠切片进行Pax6和AP - 2α表达模式的共定位检测。为了测试这两种转录因子之间的潜在协同作用,将分别对编码Pax6或AP - 2α的基因杂合的两种小鼠品系进行杂交,以产生双杂合的Pax6(+/lacZ)/AP - 2α(+/-)小鼠。然后对胚胎期和出生后的切片进行组织学检查,以便将双杂合的Pax6(+/lacZ)/AP - 2α(+/-)眼与单杂合子眼和野生型眼进行比较。

结果

对发育阶段的检查显示,Pax6和AP - 2α蛋白在前晶状体上皮中有明显的共定位。然而,Pax6的表达在晶状体的过渡区持续更久,而AP - 2α的表达在晶状体上皮细胞分化为纤维细胞的区域之前就停止了。对胚胎期和出生后的突变小鼠眼进行组织学研究表明,虽然单Pax6杂合子小鼠表现出角膜 - 晶状体粘连的残余,但晶状体和角膜在物理上是分离的。相比之下,Pax6(+/lacZ)/AP - 2α(+/-)双杂合子显示出一个明显的晶状体柄,它向角膜表面突出,形成了直接的角膜 - 晶状体附着。

结论

Pax6和AP - 2α的共定位主要在增殖的晶状体中央上皮中观察到,这也是在双杂合的Pax6(+/lacZ)/AP - 2α(+/-)眼中观察到晶状体柄表型的相同区域。与单杂合子相比,在这些双杂合小鼠中观察到的更严重的表型表明,Pax6和AP - 2α可能协同作用以控制晶状体发育。

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