兩型斑馬魚肌肉調控蛋白MRF4a與MRF4b羧端功能區之結構分析

淡江大學機構典藏 > 理學院 > 生命科學研究所 > 學位論文 > Item 987654321/32659

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题名:	兩型斑馬魚肌肉調控蛋白MRF4a與MRF4b羧端功能區之結構分析
其它题名:	Structural analysis of the c-terminal functional domains of two types of zebrafish myogenic regulatory protein, MRF4a and MRF4b
作者:	張元鳳;Chang, Yuan-fong
贡献者:	淡江大學生命科學研究所碩士班陳銘凱;Chern, Ming-kai
关键词:	MRF4;肌肉生成;酵母菌單雜合分析;MRF4;myogenesis;yeast one-hybrid system
日期:	2007
上传时间:	2010-01-11 02:31:25 (UTC+8)
摘要:	MRF4是肌肉特異性轉錄因子之一，參與肌肉芽細胞的分化及增生。先前的研究發現斑馬魚MRF4基因有不同的兩型，即MRF4a與MRF4b，而且與其他物種的肌肉轉錄因子群（MRFs）的三位成員–Myf5、MyoD及Myogenin一樣，在蛋白質結構上具有一共同的保守區域bHLH domain；近年來有研究發現另一個具功能性的蛋白序列其位於bHLH domain之後，經電腦預測為一α-helix的結構，特此命名為「Helix 3 domain」，且證實此段被預測為螺旋結構的蛋白序列於骨骼肌生成上，具有促進內生性肌肉專一性調控基因的轉錄。由於MRFs家族的羧端內「Helix 3 domain」序列具高度保留性，因此本研究選擇在斑馬魚MRFb的羧端內「Helix 3 domain」（胺基酸序列210至224）以site-directed mutagenesis PCR製造MRF4b胺基酸序列219位置Serine點突變成Proline，來測定「Helix 3 domain」突變對於二級結構所造成的影響；同時也利用酵母菌單雜合分析（yeast one-hybrid system）試圖探討「Helix 3 domain」在MRFs家族的轉錄活性上，所扮演的角色。首先利用E.coli BL21-CodonPlus（DE3）-RIL 菌株製造MRF4a羧端蛋白、MRF4b羧端突變與未突變的重組蛋白，由圓二色旋光儀（circular dichroism）的光譜分析其二級結構，結果指出此蛋白功能區存在有「β-sheet」。此外，酵母菌單雜合分析試驗中觀測宿主酵母菌GAL1-HIS3報導基因的表現情形，也發現以MRF4b全長蛋白為activation domain之報導基因，宿主酵母菌生長情況較好；故推論具有「Helix 3 domain」的MRF4b蛋白活性較高。 MRF4 belongs to the family of myogenic regulatory factors（MRFs）and participates in the differentiation and proliferation of myoblasts. Previous studies in Zebrafish indicated the existence of two different types of MRF4 gene, namely MRF4a and MRF4b. This situation is the same as the three other members of MRF family: Myf5, MyoD, Myogenin of which they share a conserved bHLH domain. Other studies indicated another functional protein sequence is present at the carboxyl end following the bHLH domain. It is predicted to be an amiphipathic α-helix, and is referred to as「Helix 3 domain」. It was also verified that this α-helix is capable of promoting expression of endogenous muscle gene during skeletal myogenesis. Because「Helix 3 domain」of carboxy-terminal region of MRFs family exhibits highly conserved sequence﹐I substituted amino acid 219 for proline in the carboxyl terminal sequence of MRF4b by site-directed mutagenesis PCR to determine any change in the secondary structure. I also utilized yeast one-hybrid analysis to investigate the role of「Helix 3 domain」in the transcription activity of MRFs. I used E.coli BL21-CodonPlus (DE3) RIL strain to produce MRF4b C-terminal protein, MRF4b C-terminal protein and MRF4b C-terminal mutant protein. I then compared the difference of secondary structures of these three different recombinant proteins by circular dichroism. The results indicated「Helix 3 domain」contains a「β-sheet」. In addition, yeast one-hybrid system utilizes GAL1-HIS3 reporter gene to observe the transcription activity of MRFs in the yeast host cell. I found MRF4b is the best of all three MRFs. I infer that MRF4b with「Helix 3 domain」has a higher activity than the other two forms of MRF.
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