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裂殖酵母中自主复制序列元件的序列分析。

Sequence analysis of ARS elements in fission yeast.

作者信息

Maundrell K, Hutchison A, Shall S

机构信息

School of Biological Sciences, University of Sussex, Brighton, UK.

出版信息

EMBO J. 1988 Jul;7(7):2203-9. doi: 10.1002/j.1460-2075.1988.tb03059.x.

Abstract

Chromosomal DNA of Schizosaccharomyces pombe contains sequences with properties analogous to ARS elements of Saccharomyces cerevisiae. Following Sau3A fragmentation of the S. pombe genome we have recovered a number of such fragments in an M13-based shuttle vector, suitable for subsequent sequence analysis. The complete nucleotide sequence has been obtained for eight ARS+ inserts derived from the Sau3A cloning and for the ARS present in pFL20 isolated previously by Losson and Lacroute (Cell, 32, 371-377, 1983). The Sau3A clones are single fragments between 0.8 and 1.8 kb. No ARS+ clones smaller than this were recovered even though the average size Sau3A fragment in S. pombe is approximately 200-300 bp. The sequence analysis revealed that all clones are AT-rich (69-75% A + T residues), and all contain a particularly AT-rich 11 bp core element represented by the consensus sequence 5' (A/T)PuTT-TATTTA(A/T) 3'. Deletion mapping indicates that the consensus in all cases is in the vicinity of a functional ARS domain. However precise excision of the consensus by in vitro mutagenesis has little effect on ARS activity as judged by the transformation assay. We argue that the association of the consensus with the ARS domain occurs too reproducibly to be explained by chance alone. We suggest that although it may not be essential for the extrachromosomal maintenance of plasmids in S. pombe, the consensus does have a function in situ in the chromosome and thus is always present as a cryptic sequence in the isolated ARS element.

摘要

粟酒裂殖酵母的染色体DNA含有与酿酒酵母ARS元件性质类似的序列。对粟酒裂殖酵母基因组进行Sau3A酶切后,我们在基于M13的穿梭载体中获得了许多这样的片段,适合后续的序列分析。我们已经获得了从Sau3A克隆得到的8个ARS⁺插入片段以及先前由洛森和拉克鲁特分离得到的pFL20中存在的ARS的完整核苷酸序列(《细胞》,第32卷,第371 - 377页,1983年)。Sau3A克隆是大小在0.8至1.8 kb之间的单个片段。即使粟酒裂殖酵母中Sau3A片段的平均大小约为200 - 300 bp,也未获得小于此大小的ARS⁺克隆。序列分析表明,所有克隆都富含AT(A + T残基占69 - 75%),并且都含有一个特别富含AT的11 bp核心元件,其共有序列为5' (A/T)PuTT - TATTTA(A/T) 3'。缺失图谱分析表明,在所有情况下,共有序列都在功能性ARS结构域附近。然而,通过体外诱变精确切除共有序列,根据转化分析判断,对ARS活性影响很小。我们认为共有序列与ARS结构域的关联出现得过于可重复,无法仅用偶然来解释。我们提出,虽然它对于粟酒裂殖酵母中质粒的染色体外维持可能不是必需的,但该共有序列在染色体原位确实具有功能,因此在分离的ARS元件中总是作为一个隐蔽序列存在。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/681e/454554/ca4b4c854f4b/emboj00144-0273-a.jpg

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