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含有鳄梨日斑类病毒两条极性链的复合体:叶绿体中的鉴定及特性分析

Complexes containing both polarity strands of avocado sunblotch viroid: identification in chloroplasts and characterization.

作者信息

Navarro J A, Darós J A, Flores R

机构信息

Instituto de Biologia Molecular y Celular de Plantas (UPV-CSIC), Universidad Politecnica de Valencia, Camino de Vera 14, Valencia, 46022, Spain.

出版信息

Virology. 1999 Jan 5;253(1):77-85. doi: 10.1006/viro.1998.9497.

Abstract

RNA analysis by nondenaturing polyacrylamide gel electrophoresis and Northern blot hybridization of avocado chloroplasts purified from protoplasts of leaves infected by avocado sunblotch viroid (ASBVd) revealed the main ASBVd-specific bands found previously in preparations of total leaf RNA: the monomeric, dimeric and subgenomic RNAs, and two bands, x and y. After RNase treatment in high ionic strength, bands x and y remained resistant, indicating a high content of double-stranded RNAs, whereas the other viroid-specific and cellular RNAs were degraded. Analysis by denaturing polyacrylamide gel electrophoresis and Northern blot hybridization showed that the major constituents of the purified y and x bands were the monomeric circular and linear ASBVd forms of both polarities, but band y contained additionally multimeric ASBVd RNAs, also of both polarities, that probably cause its slower migration in nondenaturing gels. After RNase treatment, the composition of band y was essentially unaffected, but only the monomeric linear ASBVd RNAs of both polarities was recovered from band x. However, in the presence of higher RNase concentrations, band y was converted into band x, indicating that they are closely related. The structure of complexes x and y, containing minus ASBVd strands and particularly the monomeric circular form, supports a role of replicative intermediates in the symmetric rolling circle mechanism proposed for ASBVd, whereas their localization in the chloroplast is strong evidence in favor of this organelle as the replication site of ASBVd.

摘要

通过非变性聚丙烯酰胺凝胶电泳对从感染鳄梨日斑类病毒(ASBVd)的叶片原生质体中纯化的鳄梨叶绿体进行RNA分析,并进行Northern印迹杂交,结果显示了先前在总叶RNA制剂中发现的主要ASBVd特异性条带:单体、二聚体和亚基因组RNA,以及两条条带x和y。在高离子强度下进行核糖核酸酶处理后,条带x和y仍然具有抗性,表明双链RNA含量很高,而其他类病毒特异性RNA和细胞RNA被降解。通过变性聚丙烯酰胺凝胶电泳和Northern印迹杂交分析表明,纯化的y和x条带的主要成分是两种极性的单体环状和线性ASBVd形式,但条带y还额外包含两种极性的多聚体ASBVd RNA,这可能导致其在非变性凝胶中迁移较慢。核糖核酸酶处理后,条带y的组成基本未受影响,但仅从条带x中回收了两种极性的单体线性ASBVd RNA。然而,在较高浓度核糖核酸酶存在的情况下,条带y转化为条带x,表明它们密切相关。包含负链ASBVd的复合物x和y的结构,特别是单体环状形式,支持了复制中间体在为ASBVd提出的对称滚环机制中的作用,而它们在叶绿体中的定位有力地证明了该细胞器是ASBVd的复制位点。

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