Cloning and sequence analysis of myostatin promoter in sheep

被引:31
作者
Du, R [1 ]
Chen, YF
An, XR
Yang, XY
Ma, Y
Zhang, L
Yuan, XL
Chen, LM
Qin, J
机构
[1] China Agr Univ, Coll Biol Sci, State Key Lab Agrobiotechnol, Beijing 100094, Peoples R China
[2] Shanxi Agr Univ, Coll Anim Sci & Technol, Taigu 030801, Shanxi, Peoples R China
[3] Shanxi Agr Univ, Coll Modern Educ Technol, Taigu 030801, Shanxi, Peoples R China
来源
DNA SEQUENCE | 2005年 / 16卷 / 06期
关键词
sheep; myostatin promoter; cloning; sequence analysis and comparison; transcription factor binding sites;
D O I
10.1080/10425170500226474
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To better understand the structure and function of the myostatin's gene promoter region in sheep, we cloned and sequenced a 1.517 kb fragment containing the 5'-regulatory region of the sheep myostatin gene (GenBank accession number is AY918121). The promoter sequence consists of three TATA boxes, one CAAT box, and eight putative E-boxes. Some putative muscle growth response elements for Octamer-binding factor 1(Octamer), Activator protein 1(AP1), Growth factor independence 1 zinc finger protein (Gfi-1B), Myocyte enhancer factor 2 (MEF2), Muscle-specific Mt binding site (MTBF), Glucocorticoid response elements (GRE) and Progesterone receptor binding site (PRE) were detected. Some of the motifs are conserved as compared to with that in the goat, bovine and porcine myostatin promoters. However, some differences were also found.
引用
收藏
页码:412 / 417
页数:6
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