Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/36059
標題: 以竹嵌紋病毒複製酵素的高親水性區及聚合酵素作為釣餌蛋白質利用酵母菌雙雜交篩選法尋找寄主因子
Identification of Host Factors Using the Hydrophilic Region and RNA-Dependent RNA Polymerase of Bamboo Mosaic Virus Replicase as Bait in Yeast Two-Hybrid Screen
作者: 吳慧娟
Wu, HuiChuan
關鍵字: yeast two-hybrid screen
竹嵌紋病毒
bamboo mosaic virus
酵母菌雙雜交法
出版社: 生物科技學研究所
摘要: 竹嵌紋病毒歸屬於馬鈴薯X病毒群,具單股正極的RNA基因體,含有五個轉譯架構(open reading frame,簡稱ORF)。其寄主範圍狹窄,主要感染竹類(Bambusoideae)、少數單子葉植物及菸草。第一轉譯架構(ORF1)可轉譯出一分子量為155 kDa的複製酵素(replicase),從N端至C端依序是戴帽酵素(capping enzyme)、似RNA解螺旋酵素 (RNA helicase-like domain)及聚合酵素(RNA-dependent RNA polymerase, RdRp)三個功能性區域。在前兩個功能性區域間,有約110個胺基酸組成的高親水性區(hydrophilic region, HR)。而proline-rich stretch 則位於後兩個功能性區域間。為了探討此高親水性區在病毒複製過程中可能扮演的角色及尋找參與病毒複製過程的細胞蛋白質因子,我們試圖以高親水性區及聚合酵素作為釣餌蛋白質(bait protein),利用酵母菌雙雜交篩選法(yeast two-hybrid screen),從菸草葉子的cDNA基因庫中找尋能與釣餌蛋白質相互作用的因子。首先,先將高親水性區及聚合酵素構築於載體上,並測試此兩個蛋白質是否適合此系統,結果顯示聚合酵素適用,但是高親水性區本身會活化報導基因,因此不適合作為釣餌蛋白質。為了避免產生此非專一性活化,我們將高親水性區序列做不同的刪除(deletion),最後則以去除N端33個胺基酸的截斷蛋白質(HRΔN)作為釣餌蛋白質。在此同時,我們也著手進行菸草葉子cDNA基因庫的構築並得到3.5×104個轉型株。以HRΔN作為釣餌蛋白質篩選菸草葉子cDNA基因庫時,有26顆菌落可在缺乏histidine培養基中生長(His+),並有β-galactosidase活性(LacZ+)。然而,將篩選到之質體送回能夠表現HRΔN之酵母菌,HIS3與LacZ二個報導基因並不被開啟,也就是說這26個轉型株皆為偽陽性,造成此結果之原因可能是高親水性區的N端33個胺基酸,是交互作用的重要區域。另一方面,以複製酵素作為釣餌蛋白質時,則有582顆菌落呈雙陽性反應(His+LacZ+)。利用定量分析法測試β-galactosidase活性,得到47個活性較強之轉殖株,將篩選到之質體送回能夠表現RdRp之酵母菌中,25個clones與RdRp具有專一性交互作用,將這些clones解序之後,與蛋白質資料庫比對,發現可將這些蛋白質分成四類:包括光合作用相關之蛋白質、壓力誘導產生之蛋白質、ubiquitin-proteasome pathway相關之蛋白質及未知功能之蛋白質。未來,我們將以其他生化分析法來確認這些交互作用。而這些與RdRp交互作用之蛋白質如何影響植物之生理功能或是調控病毒的複製,仍需進一步研究探討。
Bamboo mosaic virus (BaMV), a member of the potexvirus group, contains a single-stranded, positive sense RNA genome with five open reading frames (ORFs) and infects primarily members of the Bambusoideae, few other monocotyledonous plants and Nicotiana benthamiana. ORF1 encodes a 155-kDa replicase divided into capping enzyme, RNA helicase-like domain, and RNA-dependent RNA polymerase (RdRp) on the order of from N to C termini. Between the first two domains is a highly hydrophilic region (HR) with approximate 110 amino acids, while a proline-rich stretch sits between the latter two domains. To investigate the potential role of the hydrophilic region and search for cellular proteins involved in the viral replication, yeast two-hybrid screening against a leaf cDNA library of N. benthamiana is being employed by using the hydrophilic region and RdRp as bait. At first, the bait plasmids were constructed. RdRp was a well-behaved bait, but the hydrophilic region itself can transactivate the reporter genes (HIS3 lacZ). To avoid the nonspecific activation activity, the hydrophilic region was variously truncated, and finally the one with 33 amino acids deleted at N terminus (HRΔN) was used as bait in yeast two-hybrid screen. In the meanwhile, a leaf cDNA library containing 3.5×104 clones of N. benthamiana was constructed. Using HRΔN as bait to screen the leaf cDNA library, 26 colonies could grow up on minimal medium that lacked histidine (His+) and showed β-galactosidase activity (LacZ+). However, when putative interactors were retrieved and retested the ability of the two-hybrid proteins to interact specifically by retransforming to yeast, both of HIS3 and LacZ reporter genes could not be activated. It meant that all of 26 clones were false positive. This may result from the deletion of the N terminus of HR. On the other hand, 582 double-positive colonies (His+ LacZ+) were obtained when RdRp was used as bait. Using quantitative assay of β-galactosidase activity, 47 clones showed stronger interaction. By retrieving these putative interactors and retransforming to yeast to test the specific interaction, 25 clones can specifically interact with RdRp. Then the nucleotide sequences of these clones were determined and their deduced amino acid were searched in database. As a result, their encoded proteins have homology with four class proteins including photosynthesis related proteins, stress induced proteins, ubiquitin-proteasome pathway related proteins and unknown function proteins. In the future, biochemical assay will have to be performed to confirm these interactions. And how these proteins interacted with RdRp to affect the growth of the host plant or regulate virus replication? They also have to be further investigated.
URI: http://hdl.handle.net/11455/36059
Appears in Collections:生物科技學研究所

文件中的檔案:

取得全文請前往華藝線上圖書館



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.