Pal Amita, Chakrabarti Arunabha, Basak Jolly
Plant Molecular and Cellular Genetics, Bose Institute, P 1/12 CIT Scheme VIIM, Kolkata 700054, India.
J Theor Biol. 2007 Jun 7;246(3):564-73. doi: 10.1016/j.jtbi.2007.01.013. Epub 2007 Jan 25.
The Gemini viruses are a group of plant infectious agents, of which mungbean yellow mosaic India virus (MYMIV) belongs to the bipartite subgroup of Gemini virus and causes serious yield penalty in the leguminous group of plants. In this investigation we have isolated two resistant gene homologues (RGHs; AY301990, AY301991) from two MYMIV-resistant lines of Vigna mungo and V. radiata that have high homology with a MYMIV-resistant linked marker, VMYR1 (AY 297425). These three resistance factors also have similarity with 221 reported R gene/RGH sequences in the NB-ARC domain of the family Fabaceae. NB-ARC domain is an ancient, highly conserved domain of a class of plant disease resistance genes/proteins. Out of 221 in silico translated protein sequences, multialignment of 188 sequences without large insertion or truncation, unlike that of the rest 33, illustrated presence of both TIR and non-TIR subfamilies of NB-ARC domain. A critical analysis of these sequences revealed eight new conserved motifs, in addition to the reported conserved motifs within the NB-ARC domains, which are hitherto not reported. Further analysis of these eight motifs with the aid of PRINTS and PROSITE databases revealed signatures of geminiviral coat protein (GVCP) within the favoured allele, R gene or RGHs. GVCP signatures are absent within the NB-ARC domain of three species of Medicago, which are non-host to Gemini virus. These observations tempted us to predict probable mechanism of integration of GVCP within the plant R gene/RGHs and their implications in conferring geminiviral disease resistance to the host plants. Our conjecture is that these signatures were integrated during plant pathogen interaction and are being maintained within this conserved domain through active selection of the favoured allele. We comprehensively addressed the biological significance of GVCP signatures, which probably provides additional defense against Gemini viruses through degradation of homologous transcript of the virus.
双生病毒是一类植物感染因子,其中绿豆黄花叶印度病毒(MYMIV)属于双生病毒的二分体亚组,会给豆科植物群体造成严重的产量损失。在本研究中,我们从两个抗MYMIV的黑绿豆和绿豆品系中分离出了两个抗性基因同源物(RGHs;AY301990、AY301991),它们与一个抗MYMIV连锁标记VMYR1(AY 297425)具有高度同源性。这三个抗性因子在豆科植物的NB-ARC结构域中也与221个已报道的R基因/RGH序列具有相似性。NB-ARC结构域是一类植物抗病基因/蛋白质的古老且高度保守的结构域。在221个通过计算机翻译的蛋白质序列中,188个无大的插入或截断的序列的多序列比对,与其余33个序列不同,显示出NB-ARC结构域的TIR和非TIR亚家族都存在。对这些序列的严格分析揭示了除NB-ARC结构域内已报道的保守基序外的八个新的保守基序, 这些基序迄今尚未见报道。借助PRINTS和PROSITE数据库对这八个基序的进一步分析揭示了在有利等位基因、R基因或RGHs中存在双生病毒外壳蛋白(GVCP)的特征。在三种对双生病毒无宿主反应的苜蓿属植物的NB-ARC结构域中不存在GVCP特征。这些观察结果促使我们预测GVCP整合到植物R基因/RGHs中的可能机制及其对宿主植物赋予双生病毒病抗性的影响。我们推测这些特征是在植物与病原体相互作用期间整合进去的,并通过对有利等位基因的积极选择而在这个保守结构域中得以保留。我们全面探讨了GVCP特征的生物学意义,其可能通过降解病毒的同源转录本为抵御双生病毒提供额外的防御。