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香蕉束顶病毒基因组中的一段重复序列对高效复制至关重要。

An iterated sequence in the genome of Banana bunchy top virus is essential for efficient replication.

作者信息

Herrera-Valencia Virginia A, Dugdale Benjamin, Harding Robert M, Dale James L

机构信息

Science Research Centre, Queensland University of Technology, GPO Box 2434, Brisbane, QLD 4001, Australia.

出版信息

J Gen Virol. 2006 Nov;87(Pt 11):3409-3412. doi: 10.1099/vir.0.82166-0.

Abstract

Banana bunchy top virus (BBTV) has a multi-component genome of circular, single-stranded DNA. BBTV replicates via a rolling-circle mechanism, probably involving sequence-specific interaction of the replication initiation protein (Rep) with iterated sequences (iterons) within the viral genome. Three putative iterons (designated F1, F2 and R), with the sequence GGGAC, have been identified in the intergenic region of each BBTV component. To investigate their role in replication, each of the iterons was mutated, singularly and in tandem, in a BBTV DNA-N 1.1mer and the ability of these molecules to be replicated by the BBTV 'master' Rep was evaluated in banana cells using transient biolistic assays. All iteron mutants were replicated less efficiently than the native DNA-N. Mutation of the F1 and R iterons caused a 42 and 62 % reduction in DNA-N replication, respectively, whereas mutation of the F2 and combined F1F2 iteron virtually abolished DNA-N replication.

摘要

香蕉束顶病毒(BBTV)具有由环状单链DNA组成的多组分基因组。BBTV通过滚环机制进行复制,这可能涉及复制起始蛋白(Rep)与病毒基因组内重复序列(迭代子)的序列特异性相互作用。在每个BBTV组分的基因间隔区已鉴定出三个假定的迭代子(命名为F1、F2和R),其序列为GGGAC。为了研究它们在复制中的作用,在BBTV DNA-N 1.1聚体中对每个迭代子进行了单独和串联突变,并使用瞬时生物弹道测定法在香蕉细胞中评估了这些分子被BBTV“主”Rep复制的能力。所有迭代子突变体的复制效率均低于天然DNA-N。F1和R迭代子的突变分别导致DNA-N复制减少42%和62%,而F2和组合的F1F2迭代子的突变几乎完全消除了DNA-N复制。

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