Suppr超能文献

小鼠遗传学与分子生物学在冷泉港交汇。由美国纽约冷泉港实验室主办的小鼠分子遗传学会议,1990年8月29日至9月2日于冷泉港召开。

Mouse genetics meets molecular biology at Cold Spring Harbor. Mouse Molecular Genetics sponsored by the Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, USA, August 29-September 2, 1990.

作者信息

Wagner E F

机构信息

Research Institute of Molecular Pathology, (IMP), Vienna, Australia.

出版信息

New Biol. 1990 Dec;2(12):1071-4.

PMID:2088499
Abstract

As stated earlier, the digestion of roughly 100 short talks delivered within a few days and containing very condensed information is, even for experts, quite demanding. Sometimes one felt in danger of becoming "psyched out" by all the experiments described; perhaps smaller group discussions dealing with experiments that have not worked, as well as the elimination of redundancies in the presentations, would have added to the flavor of the meeting. But what is the "take home message" from the 1990 CSH Mouse Meeting? With all the described breakthroughs, has mouse molecular genetics and development arrived at a turning point? I am inclined to answer this question with a "yes" on the basis of the following considerations: The elegant studies of development in Drosophila and Caenorhabditis elegans were made possible by the power of genetics with the use of developmental mutations. These studies taught us that the sequential activation of a hierarchy of regulatory genes dictates the temporal and spatial patterns of expression of proteins that define cell phenotypes and the body plan, and thereby control development. With the identification of important regulatory genes responsible for many classical as well as experimentally induced mouse mutations, in conjunction with traditional transgenic studies and the power of deleting and altering genes via ES cell chimeras, the study of mouse development has now gained an important new dimension. It is feasible that the consequences of subtle but precise genetic changes, such as the modification of regulatory elements or DNA-binding domains, can be studied in the whole organism by use of ES cells.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

如前所述,要消化在几天内发表的大约100场简短演讲,且这些演讲包含非常精炼的信息,即便对于专家来说,要求也颇高。有时,人们会觉得自己有被所描述的所有实验弄得“不知所措”的危险;或许安排一些规模较小的小组讨论,探讨那些未成功的实验,以及减少演讲中的冗余内容,会为会议增添更多趣味。但是,1990年冷泉港小鼠会议的“关键信息”是什么呢?鉴于所有已描述的突破,小鼠分子遗传学与发育研究是否已迎来转折点?基于以下几点考虑,我倾向于给出肯定的回答:利用发育突变,遗传学的强大力量使得对果蝇和秀丽隐杆线虫发育的精妙研究成为可能。这些研究让我们明白,调控基因层级的顺序激活决定了定义细胞表型和身体蓝图的蛋白质表达的时空模式,从而控制发育。随着负责许多经典以及实验诱导的小鼠突变的重要调控基因的鉴定,结合传统的转基因研究以及通过胚胎干细胞嵌合体删除和改变基因的能力,小鼠发育研究如今获得了一个重要的新维度。利用胚胎干细胞在完整生物体中研究细微但精确的基因变化(如调控元件或DNA结合结构域的修饰)所产生的后果是可行的。(摘要截选至250词)

相似文献

4
Generation of chimeras by microinjection.
Methods Mol Biol. 2009;561:199-217. doi: 10.1007/978-1-60327-019-9_13.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验