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  1. NTU Theses and Dissertations Repository
  2. 生命科學院
  3. 生化科技學系
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/15752
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor王愛玉
dc.contributor.authorHao-Chun Changen
dc.contributor.author張皓鈞zh_TW
dc.date.accessioned2021-06-07T17:51:23Z-
dc.date.copyright2012-10-12
dc.date.issued2012
dc.date.submitted2012-09-26
dc.identifier.citationBrown CJ, Johnson AK, Dunker AK, Daughdrill GW (2011) Evolution and disorder. Curr Opin Struc Biol 21: 441-446
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Dunker AK (2004) Instrinsically disordered protein and cell signaling. Biophysical Journal 86: 354a-355a
Dunker AK, Brown CJ, Lawson JD, Iakoucheva-Sebat LM, Vucetic S, Obradovic Z (2002a) The protein trinity: Structure/function relationships that include intrinsic disorder. Biophysical Journal 82: 460a-460a
Dunker AK, Brown CJ, Lawson JD, Iakoucheva LM, Obradovic Z (2002b) Intrinsic disorder and protein function. Biochemistry 41: 6573-6582
Dunker AK, Brown CJ, Obradovic Z (2002c) Identification and functions of usefully disordered proteins. Adv Protein Chem 62: 25-49
Dunker AK, Lawson JD, Brown CJ, Williams RM, Romero P, Oh JS, Oldfield CJ, Campen AM, Ratliff CR, Hipps KW, Ausio J, Nissen MS, Reeves R, Kang CH, Kissinger CR, Bailey RW, Griswold MD, Chiu M, Garner EC, Obradovic Z (2001) Intrinsically disordered protein. J Mol Graph Model 19: 26-59
Dunker AK, Obradovic Z (2001) The protein trinity - linking function and disorder. Nat Biotechnol 19: 805-806
Dunker AK, Uversky VN, Oldfield CJ, Mohan A, Cheng Y, Zaidi S, Romero PR, Xie H, Obradovic Z (2007) Intrinsically disordered proteins. Journal of Molecular Graphics and Modelling 19:26 –59
Dyson HJ, Wright PE (2005) Intrinsically unstructured proteins and their functions. Nat Rev Mol Cell Bio 6: 197-208
Fink AL (2005) Natively unfolded proteins. Curr Opin Struc Biol 15: 35-41
Gunasekaran K, Tsai CJ, Nussinov R (2004) Analysis of ordered and disordered protein complexes reveals structural features discriminating between stable and unstable monomers. J Mol Biol 341: 1327-1341
He B, Wang KJ, Liu YL, Xue B, Uversky VN, Dunker AK (2009) Predicting intrinsic disorder in proteins: an overview. Cell Res 19: 929-949
Hebrard E, Bessin Y, Michon T, Longhi S, Uversky VN, Delalande F, Van Iakoucheva LM, Brown CJ, Lawson JD, Obradovic Z, Dunker AK (2002) Intrinsic disorder in cell-signaling and cancer-associated proteins. J Mol Biol 323: 573-584
Iakoucheva LM, Dunker AK (2003) Order, disorder, and flexibility: Prediction from protein sequence. Structure 11: 1316-1317
Lehrach H, Diamond D, Wozney JM, Boedtker H (1977) RNA molecular weight determinations by gel electrophoresis under denaturing conditions, a critical reexamination. Biochemistry 16: 4743-4751
Obradovic Z, Peng K, Vucetic S, Radivojac P, Brown CJ, Dunker AK (2003) Predicting intrinsic disorder from amino acid sequence. Proteins-Structure Function and Genetics 53: 566-572
Radivojac P, Obradovic Z, Smith DK, Zhu G, Vucetic S, Brown CJ, Lawson JD, Dunker AK (2004) Protein flexibility and intrinsic disorder. Protein Sci 13: 71-80
Romero P, Obradovic Z, Li XH, Garner EC, Brown CJ, Dunker AK (2001) Sequence complexity of disordered protein. Proteins-Structure Function and Genetics 42: 38-48
Sambrook J, Russell DW (2001) Molecular Cloning : A Laboratory Manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.
Shimizu K, Toh H (2009) Interaction between Intrinsically Disordered Proteins Frequently Occurs in a Human Protein-Protein Interaction Network. J Mol Biol 392: 1253-1265
Tompa P (2002) Intrinsically unstructured proteins. Trends Biochem Sci 27: 527-533
Towbin H, Staehelin T, Gordon J (1979) Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. PNAS 76: 4350-4354
Uversky VN (2009) Intrinsically Disordered Proteins and Their Environment: Effects of Strong Denaturants, Temperature, pH, Counter Ions, Membranes, Binding Partners, Osmolytes, and Macromolecular Crowding. Protein J 28: 305-325
Uversky VN, Oldfield CJ, Dunker AK (2005) Showing your ID: intrinsic disorder as an ID for recognition, regulation and cell signaling. J Mol Recognit 18: 343-384
Vucetic S, Obradovic Z, Vacic V, Radivojac P, Peng K, Iakoucheva LM, Cortese MS, Lawson JD, Brown CJ, Sikes JG, Newton CD, Dunker AK (2005) DisProt: a database of protein disorder. Bioinformatics 21: 137-140
Vucetic S, Xie HB, Iakoucheva LM, Oldfield CJ, Dunker AK, Obradovic Z, Uversky VN (2007) Functional anthology of intrinsic disorder. 2. Cellular components, domains, technical terms, developmental processes, and coding sequence diversities correlated with long disordered regions. J Proteome Res 6: 1899-1916
Ward JJ, Sodhi JS, McGuffin LJ, Buxton BF, Jones DT (2004) Prediction and functional analysis of native disorder in proteins from the three kingdoms of life. J Mol Biol 337: 635-645
Xie HB, Vucetic S, Iakoucheva LM, Oldfield CJ, Dunker AK, Obradovic Z, Uversky VN (2007a) Functional anthology of intrinsic disorder. 3. Ligands, post-translational modifications, and diseases associated with intrinsically disordered proteins. J Proteome Res 6: 1917-1932
Xie HB, Vucetic S, Iakoucheva LM, Oldfield CJ, Dunker AK, Uversky VN, Obradovic Z (2007b) Functional anthology of intrinsic disorder. 1. Biological processes and functions of proteins with long disordered regions. J Proteome Res 6: 1882-1898
林維治 (1994) 林維治先生竹類論文集. 林業叢刊第69號,張添榮主編,台灣省林業試驗所
莊榮輝 (1999) 酵素化學實驗.實驗操作手冊,國立台灣大學
葉勝雄 (2011) 在綠竹生長過程中差異性表現基因之檢定. 博士論文,國立台灣大學
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/15752-
dc.description.abstract竹類植物通常具有快速生長的特性。本研究以綠竹 (Bambusa oldhamii) 的cDNA以及genomic DNA為模版進行PCR,選殖出一個在快速延長的綠竹節間受到正調控的未知功能的ORF。將其cDNA及genomic DNA序列進行比對,可以發現兩者之核苷酸序列及胺基酸序列不完全相同但同質度高,顯示兩者為同源基因,並且得知在ORF中沒有intron的存在;兩者的序列轉譯後得到的蛋白質分子量皆為40.8 kDa ,序列長度為354個胺基酸。以BLAST進行分析發現,在目前的基因庫中只比對到單子葉植物的相似序列,並且功能未知,因此將此二同源基因分別命名為BoMSP41-1 (Bambusa oldhamii中的蛋白質monocot specific protein,分子量為41 kDa) 及BoMSP41-2。兩種BoMSP41胺基酸序列中皆富含Gln、Glu以及其他帶電荷的胺基酸Lys、Arg、Asp,但是缺少Trp。此外,亦存在一些重複序列。藉由PONDR軟體預測結果,顯示兩種BoMSP41都具有一段的結構不穩定區段,因此推測其為intrinsically disordered proteins。另外BoMSP41-1的表現以real-time PCR分析,發現BoMSP41-1mRNA在快速延長中的節間中的表現量大幅增加,因此推測該基因在綠竹生長中扮演了重要的角色。zh_TW
dc.description.abstractGrowth of bamboo is generally faster than other plants. The coding region of an function-unknown gene, which was shown to be up-regulated in the rapidly elongating bamboo culms, was cloned from the shoots of Bambusa oldhamii using PCR with genomic DNA and cDNAs from bamboo shoots as templates. Alignment of the genomic sequence and cDNA sequence of this gene showed that they were homologs with high identities in both the nucleotide and amino acid sequences, and there was no intron within the open reading frames. Both sequences encoded a 40.8-kDa polypeptide of 354 amino acid residues. BLAST searching revealed that they might be monocot-specific and that the function of there homologs in other plants remained unknown. They were designated BoMSP41-1 (for monocot-specific protein of 41 kDa in Bambusa oldhamii) and BoMSP41-2, respectively. The deduced amino acid sequences of BoMSP41-1 and BoMSP41-2 were rich in Gln and Glu, and other charged amino acid residues Lys, Arg and Asp, but was lacking inTrp. In addition, several tandemly repeated sequences were identify . A long disorder region with high probability was predicted in each BoMSP41 by the disorder prediction program PONDR, suggesting that they were intrinsically disordered proteins. The expression of BoMSP41-2 analyzed by real-time RT-PCR showed that the increase in BoMSP41-1 mRNA abundance paralleled the elongation rate of bamboo culms, indicating that the gene plays an important role in bamboo growth.en
dc.description.provenanceMade available in DSpace on 2021-06-07T17:51:23Z (GMT). No. of bitstreams: 1
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Previous issue date: 2012
en
dc.description.tableofcontents目錄
摘要 i
Abstract ii
縮寫表 iv
目錄 vi
第一章 研究背景 - 1 -
1.1 竹 - 1 -
1.2 先前研究 - 2 -
1.3 本實驗的目的與策略 - 3 -
第二章 實驗材料與方法 - 4 -
2.1 實驗材料 - 4 -
2.1.1 生長中的綠竹樣品 - 4 -
2.1.2 菌種 - 5 -
2.1.3 質體 - 5 -
2.2 實驗藥品與儀器 - 6 -
2.2.1 實驗藥品 - 6 -
2.2.2 實驗儀器 - 6 -
2.3 實驗方法 - 8 -
2.3.1 Real-time PCR分析 - 8 -
2.3.2 aa23100m-1的選殖 - 10 -
2.3.3 TA cloning建立重組質體 - 12 -
2.3.4 重組質體之轉形株篩選與鑑定 - 12 -
2.3.5 BoMSP41 胺基酸序列分析 - 15 -
2.3.6 表現質體構築 - 16 -
2.3.7 BoMSP41重組蛋白質之表現 - 16 -
2.3.8 蛋白質電泳 - 17 -
2.3.9 Coomassie Blue染色法 - 17 -
2.3.10 Western 轉印分析 - 17 -
2.3.11 Codon usage分析 - 18 -
2.3.12 Codon usage改變的MSP41核苷酸序列合成 - 18 -
2.3.13 pET22b-eMSP41的建構 - 19 -
第三章 結果與討論 - 20 -
3.1 目標基因之找尋 - 20 -
3.2 目標基因全長ORF的選殖 - 20 -
3.3 MSP41胺基酸序列分析與功能探索 - 21 -
3.4 BoMSP41重組蛋白質表現 - 23 -
3.4.1 表現質體的建構 - 23 -
3.4.2 重組蛋白質的表現 - 23 -
3.4.3 Codon usage分析 - 23 -
3.4.4 全基因合成後表現 - 24 -
第四章 未來展望 - 25 -
4.1 BoMSP41在細胞內的定位 - 25 -
4.2 BoMSP41與快速生長的相關性 - 25 -
4.3 BoMSP41是IDP? - 25 -
4.4 BoMSP41與其他蛋白質之交互作用 - 25 -
圖一 aa23100m-1之核苷酸序列與推衍出之胺基酸序列 - 32 -
圖二 以Real-time PCR分析aa23100m-1在生長中綠竹之表現量 - 33 -
圖三 aa23100m-1核苷酸序列與其他禾本科植物之相似序列之比對 - 34 -
圖四 全長aa23100m-1 ORF之增殖 - 35 -
圖五 aa23100m-1-1及aa23100m-1-2的核苷酸序列比對 - 36 -
圖六 BoMSP41-1 (aa23100m-1-1) 核苷酸序列與推衍之胺基酸序列 - 37 -
圖七 BoMSP41-2與其他禾本科植物相似基因之核苷酸序列比對 - 39 -
圖八 BoMSP41-2與其他禾本科植物相似基因之胺基酸序列比對 - 40 -
圖九 BoMSP41-2 disoder region的分析 - 41 -
圖十 於pET16b-MSP41/Rosetta gami B菌株中進行重組BoMSP41之表現 - 42 -
圖十一 BoMSP41的codons於大腸桿菌中的使用情形 - 43 -
圖十二 eMSP41重組蛋白質之表現 - 44 -
表一 由綠竹EST library 中挑出之候選基因 - 45 -
表二 BoMSP41-2胺基酸組成 - 45 -
dc.language.isozh-TW
dc.subject無穩定構型蛋白質zh_TW
dc.subject竹生長發育zh_TW
dc.subject綠竹zh_TW
dc.subject單子葉植物zh_TW
dc.subject快速生長zh_TW
dc.subjectBambusa MSP41en
dc.subjectintrinsically disordered proteinen
dc.subjectBambusa oldhamiien
dc.subjectbamboo growthen
dc.subjectmonocoten
dc.title綠竹中 BoMSP41 基因之分子選殖與檢定zh_TW
dc.titleMolecular cloning and characterization of BoMSP41 in
Bambusa oldhamii
en
dc.typeThesis
dc.date.schoolyear101-1
dc.description.degree碩士
dc.contributor.oralexamcommittee宋賢一,楊健志,廖憶純
dc.subject.keyword竹生長發育,綠竹,單子葉植物,快速生長,無穩定構型蛋白質,zh_TW
dc.subject.keywordbamboo growth,monocot,Bambusa MSP41,Bambusa oldhamii,intrinsically disordered protein,en
dc.relation.page45
dc.rights.note未授權
dc.date.accepted2012-09-26
dc.contributor.author-college生命科學院zh_TW
dc.contributor.author-dept生化科技學系zh_TW
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