Moephuli S R, Klein N W, Baldwin M T, Krider H M
Center for Environmental Health, University of Connecticut, Storrs 06269, USA.
Proc Natl Acad Sci U S A. 1997 Jan 21;94(2):543-8. doi: 10.1073/pnas.94.2.543.
Research has previously shown that, without methionine supplements, neural tube proteins of rat embryos cultured on bovine sera were hypomethylated and neural tubes failed to close. In the present study, to identify the proteins that became methylated during neurulation, rat embryos were first cultured on methionine-deficient bovine serum for 40 hr, then incubated with puromycin for 1 hr, and, finally, incubated with [methyl-14C]methionine and puromycin for 5 hr. On the basis of molecular weights, isoelectric points, and Western immunoblots, the methyl-14C-labeled proteins were identified as actin, alpha beta-tubulin, and neurofilament L. Indirect immunofluorescence studies indicated that without the addition of methionine to the culture, localization of actin and alpha beta-tubulin in the basal cytoplasm did not occur and these neuroepithelial cells lost their columnar morphology.
先前的研究表明,在没有甲硫氨酸补充剂的情况下,培养在牛血清上的大鼠胚胎神经管蛋白会发生低甲基化,并且神经管无法闭合。在本研究中,为了鉴定在神经胚形成过程中发生甲基化的蛋白质,首先将大鼠胚胎在缺乏甲硫氨酸的牛血清中培养40小时,然后与嘌呤霉素孵育1小时,最后与[甲基-14C]甲硫氨酸和嘌呤霉素孵育5小时。根据分子量、等电点和蛋白质免疫印迹法,将甲基-14C标记的蛋白质鉴定为肌动蛋白、αβ-微管蛋白和神经丝L。间接免疫荧光研究表明,在培养基中不添加甲硫氨酸的情况下,肌动蛋白和αβ-微管蛋白不会定位在基底细胞质中,并且这些神经上皮细胞失去了柱状形态。