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分析一种新的双生病毒揭示了 CP 基因启动子中保守的复合元件,该元件存在于几个 Geminiviridae 属中:理解晚期基因复杂调控的线索。

Analysis of a new begomovirus unveils a composite element conserved in the CP gene promoters of several Geminiviridae genera: Clues to comprehend the complex regulation of late genes.

机构信息

División de Biología Molecular, Instituto Potosino de Investigación Científica y Tecnológica A. C., San Luis Potosí, SLP, México.

CONACYT-CIIDZA-Instituto Potosino de Investigación Científica y Tecnológica A. C., San Luis Potosí, SLP, México.

出版信息

PLoS One. 2019 Jan 23;14(1):e0210485. doi: 10.1371/journal.pone.0210485. eCollection 2019.

DOI:10.1371/journal.pone.0210485
PMID:30673741
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6344024/
Abstract

A novel bipartite begomovirus, Blechum interveinal chlorosis virus (BleICV), was characterized at the genome level. Comparative analyses revealed that BleICV coat protein (CP) gene promoter is highly divergent from the equivalent region of other begomoviruses (BGVs), with the single exception of Tomato chino La Paz virus (ToChLPV) with which it shares a 23-bp phylogenetic footprint exhibiting dyad symmetry. Systematic examination of the homologous CP promoter segment of 132 New World BGVs revealed the existence of a quasi-palindromic DNA segment displaying a strongly conserved ACTT-(N7)-AAGT core. The spacer sequence between the palindromic motifs is constant in length, but its sequence is highly variable among viral species, presenting a relaxed consensus (TT)GGKCCCY, which is similar to the Conserved Late Element or CLE (GTGGTCCC), a putative TrAP-responsive element. The homologous CP promoter region of Old World BGVs exhibited a distinct organization, with the putative TATA-box overlapping the left half of the ACTT-N7 composite element. Similar CP promoter sequences, dubbed "TATA-associated composite element" or TACE, were found in viruses belonging to different Geminiviridae genera, hence hinting unsuspected evolutionary relationships among those lineages. To get cues about the TACE function, the regulatory function of the CLE was explored in distinct experimental systems. Transgenic tobacco plants harboring a GUS reporter gene driven by a promoter composed by CLE multimers expressed high beta-glucuronidase activity in absence of viral factors, and that expression was increased by begomovirus infection. On the other hand, the TrAP-responsiveness of a truncated CP promoter of Tomato golden mosaic virus (TGMV) was abolished by site-directed mutation of the only CLE present in it, whereas the artificial addition of one CLE to the -125 truncated promoter strongly enhanced the transactivation level in tobacco protoplasts. These results indicate that the CLE is a TrAP-responsive element, hence providing valuable clues to interpret the recurrent association of the CLE with the TACE. On the basis of the aforesaid direct evidences and the insights afforded by the extensive comparative analysis of BleICV CP promoter, we propose that the TACE might be involved in the TrAP-mediated derepression of CP gene in vascular tissues.

摘要

一种新型二分体番茄黄曲叶病毒(Blechum interveinal chlorosis virus,BleICV)在基因组水平上得到了特征描述。比较分析显示,BleICV 外壳蛋白(CP)基因启动子与其他番茄黄曲叶病毒(BGVs)的等效区域高度不同,唯一的例外是与 Tomato chino La Paz virus(ToChLPV)共享具有二分对称的 23 个碱基对的系统发育足迹。对 132 种新世界 BGVs 的同源 CP 启动子片段进行系统检查发现,存在一个准回文 DNA 片段,显示出强烈保守的 ACTT-(N7)-AAGT 核心。回文模体之间的间隔序列长度恒定,但在病毒种间序列高度可变,呈现松弛共识(TT)GGKCCCY,类似于保守晚期元件或 CLE(GTGGTCCC),这是一种推定的 TrAP 反应元件。旧世界 BGVs 的同源 CP 启动子区表现出明显的组织形式,推定的 TATA 框与 ACTT-N7 复合元件的左半部分重叠。在属于不同双生病毒科属的病毒中发现了类似的 CP 启动子序列,被称为“TATA 相关复合元件”或 TACE,这暗示了这些谱系之间存在意想不到的进化关系。为了了解 TACE 的功能,在不同的实验系统中探索了 CLE 的调节功能。含有由 CLE 多聚体组成的启动子驱动的 GUS 报告基因的转基因烟草植物在没有病毒因子的情况下表达高水平的β-葡萄糖醛酸酶活性,并且该表达在 BGV 感染时增加。另一方面,通过对存在于其中的唯一 CLE 进行定点突变,番茄金黄花叶病毒(TGMV)截短 CP 启动子的 TrAP 反应性丧失,而向 -125 截断启动子中添加一个 CLE 强烈增强了烟草原生质体中的转录激活水平。这些结果表明,CLE 是一个 TrAP 反应元件,因此为解释 CLE 与 TACE 的反复关联提供了有价值的线索。基于上述直接证据以及对 BleICV CP 启动子的广泛比较分析提供的见解,我们提出 TACE 可能参与血管组织中 CP 基因的 TrAP 介导去阻遏。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b6c/6344024/95beed67f576/pone.0210485.g010.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b6c/6344024/ecd6cd118a55/pone.0210485.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b6c/6344024/2b63c39e36ec/pone.0210485.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b6c/6344024/bdf6796b3cc2/pone.0210485.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b6c/6344024/1a19ee3f6aa3/pone.0210485.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b6c/6344024/7b6ea8f04f02/pone.0210485.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b6c/6344024/d0ed84d9be2b/pone.0210485.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b6c/6344024/49f15e494d91/pone.0210485.g009.jpg
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