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利用P转座因子进行基因破坏:果蝇基因组计划的一个重要组成部分。

Gene disruptions using P transposable elements: an integral component of the Drosophila genome project.

作者信息

Spradling A C, Stern D M, Kiss I, Roote J, Laverty T, Rubin G M

机构信息

Howard Hughes Medical Institute Research Laboratories, Carnegie Institution of Washington, Baltimore, MD 21210, USA.

出版信息

Proc Natl Acad Sci U S A. 1995 Nov 21;92(24):10824-30. doi: 10.1073/pnas.92.24.10824.

Abstract

Biologists require genetic as well as molecular tools to decipher genomic information and ultimately to understand gene function. The Berkeley Drosophila Genome Project is addressing these needs with a massive gene disruption project that uses individual, genetically engineered P transposable elements to target open reading frames throughout the Drosophila genome. DNA flanking the insertions is sequenced, thereby placing an extensive series of genetic markers on the physical genomic map and associating insertions with specific open reading frames and genes. Insertions from the collection now lie within or near most Drosophila genes, greatly reducing the time required to identify new mutations and analyze gene functions. Information revealed from these studies about P element site specificity is being used to target the remaining open reading frames.

摘要

生物学家需要遗传工具和分子工具来解读基因组信息,并最终了解基因功能。伯克利果蝇基因组计划正在通过一个大规模的基因破坏项目来满足这些需求,该项目使用单个经过基因工程改造的P转座元件来靶向果蝇基因组中的开放阅读框。对插入位点两侧的DNA进行测序,从而在物理基因组图谱上放置一系列广泛的遗传标记,并将插入与特定的开放阅读框和基因相关联。目前,该集合中的插入片段位于大多数果蝇基因内部或附近,大大减少了鉴定新突变和分析基因功能所需的时间。这些关于P元件位点特异性的研究中揭示的信息正被用于靶向其余的开放阅读框。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a844/40524/cfbb232b63cb/pnas01502-0017-a.jpg

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