Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/20624
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dc.contributor.advisor林茂森zh_TW
dc.contributor.advisorHungchen Emilie Yenen_US
dc.contributor.advisor顏宏真zh_TW
dc.contributor.author陳彥綾zh_TW
dc.contributor.authorChen, Yen-Lingen_US
dc.date2000zh_TW
dc.date.accessioned2014-06-06T07:14:05Z-
dc.date.available2014-06-06T07:14:05Z-
dc.identifier.urihttp://hdl.handle.net/11455/20624-
dc.description.abstract研究水稻品種間的親源關係有助於日後在育種上選擇親本時的考量,本實驗主要以逢機擴增多型性DNA(random amplified polymorphic DNA)來探討台灣栽培稻種間的關係,並由使用的引子中篩選核心引子;且針對特定的RAPD產物片段作分析,嘗試建立特定RAPD產物與核心引子間的關係。 本實驗共採用45個稻作種源,包含台灣省農業試驗所所提供之41個稻作種源與由日本引進的Milyang 23號,加上另外由嘉義農試所分所提供三個不同來源的越光種源,其中有13個秈稻種源、32個稉稻種源。由120條RAPD引子篩選再現性較穩定的19條引子,共產生100個標誌。數據分析發現在所有稻種間呈現62%的多型性(100個標誌,62個呈現多型性),在稉稻間呈現33.7%的多型性(86個標誌,29個呈現多型性),在秈稻間呈現52%的多型性(98個標誌,51個呈現多型性);並以樹狀圖分析造成多型性的核心引子,發現OPJ-12為主要影響品種間差異的核心引子,而以異質性來看,OPK-16是亞種間差異的核心引子。 在RAPD產物分析方面,取三段在秈稻中特有且明顯的片段,命名為IJ131800;IK16600;ID51500;將片段分別定序後與基因庫比對的結果,其中IJ13與ID5都與水稻第一條染色體有相似的片段,其中IJ13比對到一段相同度91%,ID5比對到三段相同度分別為82%、83%及96%。OPK-16的片段則是與水稻Ra基因相似,推衍氨基酸序列有約70%的相似度。Ra基因是水稻的一個轉錄因子,已知可調節花青素的生合成,目前已知位置在水稻第四條染色體上。更進一步設計gene specific primer擴增水稻基因組DNA,結果發現絕大多數的秈稻均含有此三段片段,而稉稻的基因組則缺乏此序列。 分析核心引子與秈稻特有片段之相關性發現,IK16比對到轉錄因子的基因,而OPK-16又是產生異質性最高的引子,代表OPK-16所呈現的確實是稉秈稻間多型性,且這樣大的異質性足以完整區分梗秈稻間的差異;會造成多型性如此高的原因,或許與轉錄因子Ra有關。爾後,此可提供稉秈稻外表性狀變異,與其轉錄因子調節方面作更深入的探討。zh_TW
dc.description.abstractThe knowledge of relationship between rice varieties is helpful in selecting parents for hybridization breeding program. The objectives of this study were to investigate the genetic relationship among rice varieties in Taiwan by RAPD ( random amplified polymorphic DNA), identify the core primers that are informative in estimating relationship among varities, and analyze the RAPD's fragment to evaluate the relationship between core primer and the RAPD's products. The genetic diversity of 45 rice varieties were evaluated by RAPD including 41 varieties provided by Taiwan Agricultural Research Intsitute, the Milyang 23 collected from Japan, and Koshihikari of three seed sources from Chia-Yi Agricultural Experiment Station. There were 13 Indica varieties and 32 Japonica varieties. Of the 120 primers screened, 19 were sufficient to produce 100 reproducible banding patterns. When all 19 primers were taken into consideration, 62% of banding patterns were polymorphic among all rice varieties, 33.7% were polymorphic among 32 Japonica varieties, and 52% were polymorphic among 13 Indica varieties. Based on the clustering dendrograph, the OPJ-12 was the most important core primer to differentiate varieties within the rice varieties tested. Based on the heterozygosity estimates, the OPK-16 was the core factor to affect the varieties clustering between Japonica and Indica subspecies. To analyze the RAPD's band patterns revealing potency in Indica varieties, three fragments IJ13, 1800 bp;IK16, 600 bp;and ID5, 1500 bp were cloned and sequenced. The search of the Genebank by BLAST revealed that IJ13 and ID5 had four fragments to align with on the rice chromosome 1 and the identity was 91%, 82%, 83%, and 96%. The fragment of IK16 showed 70% similarity at deduced amino acid sequence to rice transcriptional activator Ra. Ra gene encodes a transcriptional activator that regulates the anthocyanin biosynthetic pathway and has been mapped on rice chromosome 4. The primer OPK-16 not only is the core factor affecting heterozygosity, but also the OPK-16 fragment is located in the coding region of a regulatory gene. We speculated that the different morphology between Japonica and Indica may be the result of differential gene expression regulated by this transcription factor. Future studies will be focused on the novel relationship between rice phenotypes and the expression of Ra.en_US
dc.description.tableofcontents中文摘要…………………………………………1 英文摘要…………………………………………2 壹、前言…………………………………………3 貳、前人研究……………………………………6 參、材料與方法 一、試驗材料………………………………….. 16 二、DNA的萃取與定量……………………… 16 三、PCR擴增反應……………………………. 17 四、膠體電泳分析…………………………….. 18 五、數據分析………………………………….. 18 六、RAPD核心引子的篩選………………….. 19 七、RAPD片段的選殖與定序……………….. 19 八、南方墨點分析…………………………….. 21 肆、結果 一、電泳圖譜分析……………………………… 24 二、歸群與遺傳相似度分析…………………… 25 三、核心引子的篩選…………………………… 25 四、RAPD產物分析…………………………… 27 伍、討論 一、稻種間遺傳變異之探討…………………… 31 二、篩選核心引子之探討 …………………….. 35 三、片段分析結果之探討……………………… 37 陸、參考文獻…………………………………….. 41 柒、圖表………………………………………….. 48 捌、附錄………………………………………….. 71zh_TW
dc.language.isoen_USzh_TW
dc.publisher植物學系zh_TW
dc.subject逢機擴大多型性zh_TW
dc.subjectRAPDen_US
dc.subject核心引子zh_TW
dc.subject水稻zh_TW
dc.subjectcore primeren_US
dc.subjectriceen_US
dc.title台灣水稻品種核心引子之建立及分析zh_TW
dc.titleEstablishment and analysis of core sets of primers among rice varieties in Taiwan.en_US
dc.typeThesis and Dissertationzh_TW
item.openairetypeThesis and Dissertation-
item.fulltextno fulltext-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en_US-
Appears in Collections:生命科學系所
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