博碩士論文 982204017 完整後設資料紀錄

DC 欄位 語言
DC.contributor生命科學系zh_TW
DC.creator方振丞zh_TW
DC.creatorJhen-Cheng Fangen_US
dc.date.accessioned2011-7-29T07:39:07Z
dc.date.available2011-7-29T07:39:07Z
dc.date.issued2011
dc.identifier.urihttp://ir.lib.ncu.edu.tw:88/thesis/view_etd.asp?URN=982204017
dc.contributor.department生命科學系zh_TW
DC.description國立中央大學zh_TW
DC.descriptionNational Central Universityen_US
dc.description.abstractmRNA降解作用為一個重要的基因表現調控機制,參與調控基因的表現,改變胞內狀態,以因應不同外在環境的變化。Poly(A) tail deadenylation為mRNA降解的速率決定步驟,而CCR4-associated factor 1s(CAF1s)在真核生物中催化deadenylation的一個主要酵素。水稻中含有四個不同的CAF1,分別為OsCAF1A、OsCAF1B、OsCAF1G、OsCAF1H。由北方墨點法與RT-PCR的分析顯示,OsCAF1s分別受到糖及不同的非生物逆境所調控。針對rOsCAF1A與rOsCAF1B重組蛋白進行胞外活性分析,結果指出其確實具有deadenylase的活性。先前的研究指出水稻受糖調控之α-澱粉降解酶的基因,αAmy3,其mRNA的半衰期會受到糖的調控。分析有糖及缺糖培養情況下之水稻細胞αAmy3 mRNA poly(A) tail長度,結果顯示在缺糖培養時其poly(A) tail長度較有糖培養長。有趣地是,在大量表現OsCAF1A轉殖水稻懸浮細胞中,發現其參與在αAmy3 mRNA的累積。由先前研究指出,OsMYBS1與OsMYBS2被證實參與αAmy3基因的表現,分別作為正向與反向的轉錄調控因子。由此分析大量表現OsCAF1A轉殖水稻懸浮細胞OsMYBS1與OsMYBS2的表現情況,結果顯示OsMYBS1表現會大量提升而OsMYBS2表現量會因此而下降。以上結果顯示OsCAF1A參與在OsMYBS1與OsMYBS2 deadenylation過程中,進而調控αAmy3 mRNA的累積。 zh_TW
dc.description.abstractOne of central mechanisms to determine the expression level of genes for adjustment cellular status in response to various signals is messenger RNA (mRNA) degradation. Poly(A) tail deadenylation is a rate-limiting step of mRNA degradation. CCR4-associated factor 1s (CAF1s) is one of major enzymes to catalyze mRNA deadenylation in eukaryotes. Four members of CAF1 family, designated OsCAF1A, B, G and H, were analyzed and characterized in rice (Oryza sativa). Northern experiments and RT-PCR revealed diverse transcription patterns in response to sugar and various abiotic stresses among the four genes. Two recombinant proteins, rOsCAF1A and rOsCAF1B, had a deadenylation activity in vitro. It is known that mRNA half-life of αAmy3, which encodes a α-amylase, is regulated by sugar. Poly(A) tail analysis indicated that the length of poly(A) tail of αAmy3 mRNA was longer in the sugar-starved cells than in sugar-feasted cells. Interestingly, ectopic expression approach indicated that OsCAF1A was involved in αAmy3 mRNA accumulation. Previously, the OsMYBS1 and OsMYBS2 have been demonstrated to play a positive and negative regulator for αAmy3 expression, respectively. RT-PCR analysis indicated that ectopic expressed OsCAF1A caused the expression level of OsMYBS2 decreasing and the OsMYBS1 increasing. These results suggested that OsCAF1A may play a crucial role in mRNA deadenylation of OsMYBS1 and OsMYBS2 to regulate αAmy3 mRNA accumulation in rice. en_US
DC.subjectzh_TW
DC.subjectmRNA的降解zh_TW
DC.subjectα-澱粉水解酶zh_TW
DC.subjectOsMYBS2en_US
DC.subjectOsMYBS1en_US
DC.subjectα-amylaseen_US
DC.subjectCCR4-associated factor 1sen_US
DC.subjectmRNA deadenylationen_US
DC.subjectmRNA degradationen_US
DC.subjectsugaren_US
DC.title水稻CAF1基因在水稻懸浮培養細胞之研究zh_TW
dc.language.isozh-TWzh-TW
DC.titleFunctional Analysis of OsCAF1 Genes in Rice Suspension Cellsen_US
DC.type博碩士論文zh_TW
DC.typethesisen_US
DC.publisherNational Central Universityen_US

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