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C. elegans: the cell lineage and beyond

机译:秀丽隐杆线虫:细胞谱系及其他

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Thank you so very much for inviting me to be here. It gives me a mingled sense of humility at how much I owe to others, and of joy that the collective work on the worm has been recognized in this way. Among the first of my many mentors was my PhD supervisor. Colin Reese, who was developing non-aqueous methods for oligonucleotide synthesis (e.g., Fromageot et al., 1968). Colin passed me on to my postdoctoral supervisor Leslie Orgel at the Salk Institute, to work on prebiotic chemistry. The plan wasto see to what extent we could copy RNA chains without enzymes. The products were in low yield, and the challenge was to work out the sequences that had been produced. We used cutting with different ribonucleases, and chromatography to separate the fragments (e.g., Sulston et al., 1968). My introduction to C. elegans came in 1969 with my move, at Leslie's suggestion, to Sydney Brenner's group at the Medical Research Council's Laboratory of Molecular Biology (Fig. 1.). Sydney was reputed to be setting upa group to work on the nervous system of a nematode, though at that point nobody knew much about it (Brenner, 1973).
机译:非常感谢您邀请我来这里。在我欠别人多少钱的同时,这给了我一种谦卑的感觉,并以这种方式认识到蠕虫的集体工作而感到高兴。在我的许多导师中,第一位是我的博士导师。正在开发用于寡核苷酸合成的非水方法的Colin Reese(例如Fromageot等,1968)。 Colin将我转交给了Salk研究所的博士后导师Leslie Orgel,从事益生元化学研究。计划是要看在没有酶的情况下我们可以复制RNA链的程度。产品产量低,挑战在于确定已产生的序列。我们使用了不同的核糖核酸酶进行切割,然后进行色谱分离以分离这些片段(例如,Sulston等人,1968)。我对秀丽隐杆线虫的介绍是在1969年,在莱斯利的建议下,我搬到了医学研究理事会分子生物学实验室的悉尼布伦纳研究小组(图1)。众所周知,悉尼成立了一个小组来研究线虫的神经系统,尽管那时人们对此并不了解(Brenner,1973)。

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