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双链端粒DNA序列的S1核酸酶敏感性

S1 nuclease sensitivity of a double-stranded telomeric DNA sequence.

作者信息

Budarf M, Blackburn E

出版信息

Nucleic Acids Res. 1987 Aug 11;15(15):6273-92. doi: 10.1093/nar/15.15.6273.

Abstract

We examined structural properties of poly d(C4A2).d(T2G4), the telomeric DNA sequence of the ciliated protozoan Tetrahymena. Under conditions of high negative supercoiling, poly d(C4A2).d(T2G4) inserted in a circular plasmid vector was preferentially sensitive to digestion with S1 nuclease. Only the C4A2 strand was sensitive to first-strand S1 cutting, with a markedly skewed pattern of hypersensitive sites in tracts of either 46 or 7 tandem repeats. Linear poly d(C4A2).(T2G4) showed no preferential S1 sensitivity, no circular dichroism spectra indicative of a Z-DNA conformation, no unusual Tm, and no unusual migration in polyacrylamide gel electrophoresis. The S1 nuclease sensitivity properties are consistent with a model proposed previously for supercoiled poly d(CT).d(AG) (Pulleyblank et al., Cell 42:271-280, 1985), consisting of a double-stranded, protonated, right-handed underwound helix. We propose that this structure is shared by related telomeric sequences and may play a role in their biological recognition.

摘要

我们研究了纤毛原生动物四膜虫的端粒DNA序列聚d(C4A2).d(T2G4)的结构特性。在高负超螺旋条件下,插入环状质粒载体中的聚d(C4A2).d(T2G4)对S1核酸酶消化具有优先敏感性。只有C4A2链对第一链S1切割敏感,在46个或7个串联重复序列的片段中具有明显偏斜的超敏位点模式。线性聚d(C4A2).(T2G4)没有优先的S1敏感性,没有表明Z-DNA构象的圆二色光谱,没有异常的解链温度,在聚丙烯酰胺凝胶电泳中也没有异常迁移。S1核酸酶敏感性特性与先前为超螺旋聚d(CT).d(AG)提出的模型一致(Pulleyblank等人,《细胞》42:271 - 280,1985),该模型由双链、质子化、右手欠旋螺旋组成。我们提出这种结构为相关端粒序列所共有,并且可能在它们的生物学识别中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/658b/306083/8f78f3ade4cf/nar00259-0366-a.jpg

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