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三种哺乳动物晶状体纤维细胞膜蛋白的发育表达

The developmental expression of three mammalian lens fiber cell membrane proteins.

作者信息

Jarvis L J, Kumar N M, Louis C F

机构信息

Department of Biochemistry, University of Minnesota, St. Paul 55108.

出版信息

Invest Ophthalmol Vis Sci. 1993 Mar;34(3):613-20.

PMID:7680640
Abstract

PURPOSE

The expression of the lens fiber cell integral membrane proteins MP20, the alpha 3 gap junction protein (connexin 46), and MP26 (MIP) was determined both during development of the bovine fetal lens and in different animal species.

METHODS

The relative levels of the mRNA species coding for these proteins was determined by Northern blotting; this was correlated with the amounts of these proteins as determined by Western immunoblotting.

RESULTS

RNA extracted from fetal calf lenses at 3-4, 5-6, and 7-8 mo gestation, and from postnatal calf lenses, showed a progressive decrease of the mRNA species coding for MP20 (20-fold), alpha 3 gap junction protein (22-fold), and MP26 (12-fold) with development. This compared with a 6-fold decrease in total RNA and a 15-fold decrease in poly-A(+) RNA over the same period. In contrast to these significant changes in the levels of mRNA, there were no significant changes in the concentrations of these proteins over the same period. Whereas the mRNA coding for each of these proteins were concentrated in the lens cortical regions. MP20 and MP26 protein concentrations in cortical and nuclear regions were very similar. Both protein and mRNA coding for MP20, alpha 3 gap junction, and MP26 were detected in calf, sheep, pig, and rat lenses.

CONCLUSIONS

These results indicate that the expression of the mRNA coding for the lens fiber cell integral membrane proteins MP20, alpha 3 gap junction, and MP26 is regulated and may be coordinated. That the decrease in mRNA concentrations is not correlated with changes in the concentrations of these lens membrane proteins indicates their unique stability.

摘要

目的

测定牛胎儿晶状体发育过程中以及不同动物物种中晶状体纤维细胞整合膜蛋白MP20、α3缝隙连接蛋白(连接蛋白46)和MP26(MIP)的表达情况。

方法

通过Northern印迹法测定编码这些蛋白质的mRNA种类的相对水平;并将其与Western免疫印迹法测定的这些蛋白质的量进行关联。

结果

从妊娠3 - 4个月、5 - 6个月和7 - 8个月的胎牛晶状体以及出生后小牛晶状体中提取的RNA显示,随着发育,编码MP20(20倍)、α3缝隙连接蛋白(22倍)和MP26(12倍)的mRNA种类逐渐减少。相比之下,同期总RNA减少了6倍,多聚腺苷酸(+)RNA减少了15倍。与mRNA水平的这些显著变化相反,同期这些蛋白质的浓度没有显著变化。尽管编码这些蛋白质的mRNA都集中在晶状体皮质区域。皮质和核区域中MP20和MP26的蛋白质浓度非常相似。在小牛、绵羊、猪和大鼠的晶状体中均检测到编码MP20、α3缝隙连接和MP26的蛋白质和mRNA。

结论

这些结果表明,编码晶状体纤维细胞整合膜蛋白MP20、α3缝隙连接和MP26的mRNA的表达受到调控且可能是协同的。mRNA浓度的降低与这些晶状体膜蛋白浓度的变化不相关,这表明它们具有独特的稳定性。

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