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基于基因组序列寡核苷酸组成的核小体定位模式。

Nucleosome positioning pattern derived from oligonucleotide compositions of genomic sequences.

机构信息

Genome Diversity Center, Institute of Evolution, University of Haifa, Mount Carmel, Haifa 31905, Israel.

出版信息

J Biomol Struct Dyn. 2011 Feb;28(4):567-74. doi: 10.1080/07391102.2011.10531243.

Abstract

Availability of nucleosome positioning pattern(s) is crucial for chromatin studies. The matrix form of the pattern has been recently derived (I. Gabdank, D. Barash, E. N. Trifonov. J Biomol Struct Dyn 26, 403-412 (2009), and E. N. Trifonov. J Biomol Struct Dyn 27, 741-746 (2010)). In its simplified linear form it is described by the motif CGRAAATTTYCG. Oligonucleotide components of the motif (say, triplets GRA, RAA, AAA, etc.) would be expected to appear in eukaryotic sequences more frequently. In this work we attempted the reconstruction of the bendability patterns for 13 genomes by a novel approach-extension of highest frequency trinucleotides. The consensus of the patterns reconstructed on the basis of trinucleotide frequencies in 13 eukaryotic genomes is derived: CRAAAATTTTYG. It conforms to the earlier established sequence motif. The reconstruction, thus, attests to the universality of the nucleosome DNA bendability pattern.

摘要

核小体定位模式的可用性对于染色质研究至关重要。该模式的矩阵形式最近已经被推导出来(I. Gabdank、D. Barash、E. N. Trifonov. J Biomol Struct Dyn 26, 403-412 (2009),和 E. N. Trifonov. J Biomol Struct Dyn 27, 741-746 (2010))。在简化的线性形式中,它由 motif CGRAAATTTYCG 描述。该 motif 的寡核苷酸成分(例如,三核苷酸 GRA、RAA、AAA 等)预计会在真核序列中更频繁出现。在这项工作中,我们尝试通过一种新的方法——扩展最高频率的三核苷酸,来重建 13 个基因组的柔韧性模式。基于 13 个真核基因组中三核苷酸频率重建的模式的共识是:CRAAAATTTTYG。它符合早期建立的序列基序。因此,这种重建证明了核小体 DNA 柔韧性模式的普遍性。

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