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用于包装噬菌体λDNA所需的DNA序列。

DNA sequences necessary for packaging of bacteriophage lambda DNA.

作者信息

Hohn B

出版信息

Proc Natl Acad Sci U S A. 1983 Dec;80(24):7456-60. doi: 10.1073/pnas.80.24.7456.

Abstract

The extent of DNA flanking the "cohered cohesive end" site of bacteriophage lambda DNA, which is required for packaging, was determined by using defined DNA fragments and a cosmid in vivo packaging assay. From the right end of lambda DNA a 20- to 36-base-pair stretch extending from the center of the cohered cohesive ends is shown to be required, whereas the packaging efficiency of cosmids extending to 70 base pairs into the left lambda arm is reduced to 10% (compared to a fragment extending until about 80 base pairs). A 60-base-pair stretch of the left arm leaves an efficiency of only 1%. The segment thus delineated, by the nature of the assay, is both necessary and sufficient for the binding of packaging proteins to the DNA, the packaging of DNA itself, the DNA cleavage, and successful injection of the DNA into a bacterial host. By contrast, in vitro packaging of restriction fragments of mature lambda DNA directly demonstrated the selectivity of the packaging proteins for the fragment originating from the left end of the DNA. The results of the two complementary experiments are discussed in terms of the various steps before, during, and after packaging for which different sequences flanking and including the cohered cohesive ends might be required.

摘要

利用特定的DNA片段和黏粒体内包装试验,确定了噬菌体λDNA包装所需的“黏合黏性末端”位点两侧的DNA范围。从λDNA的右端起,从黏合黏性末端中心延伸出的20至36个碱基对的片段被证明是必需的,而延伸至λ左臂70个碱基对的黏粒的包装效率降至10%(与延伸至约80个碱基对的片段相比)。左臂60个碱基对的片段的包装效率仅为1%。根据试验的性质,如此划定的片段对于包装蛋白与DNA的结合、DNA自身的包装、DNA切割以及将DNA成功注入细菌宿主而言,既是必需的也是充分的。相比之下,成熟λDNA限制性片段的体外包装直接证明了包装蛋白对源自DNA左端片段的选择性。针对包装之前、期间和之后的各个步骤,讨论了这两个互补实验的结果,在这些步骤中,可能需要黏合黏性末端两侧以及包含黏合黏性末端的不同序列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f805/389970/f38a7c5aa984/pnas00650-0092-a.jpg

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