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鱼腥草中HtbZIP60基因的克隆和生物信息分析
Cloning and Bioinformatic Analysis of the Analysis of HtbZIP60 Gene in Houttuynia cordata thunb

DOI: 10.12677/BR.2024.131008, PP. 63-74

Keywords: 鱼腥草,HtbZIP60,生物信息分析,基因克隆
Houttuynia cordata thunb
, HtbZIP60, Bioinformatics Analysis, Gene Cloning

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Abstract:

bZIP是植物抗逆性领域关键的转录因子,能调控细胞生物学中的各种生命过程,包括生长、发育、应激响应和代谢调控。为了深入研究鱼腥草中bZIP60基因的功能与调控机制,以鱼腥草为材料提取总RNA,合成cDNA第一链,然后成功克隆出鱼腥草HtbZIP60基因,并对其进行相关的生物信息学分析。结果表明,HtbZIP60的编码序列全长为996 bp,编码331个氨基酸,蛋白质分子质量37447.00 ku,不含信号肽剪切位点,包含跨膜结构域,以α螺旋为主要构成,定位于细胞核,具有30个已知功能的启动子。这些发现为深入研究HtbZIP60在鱼腥草生长与发育中的生物学功能提供了科学基础。
bZIP is a key transcription factor in the field of plant stress resistance, capable of regulating various biological processes in cell biology, including growth, development, stress response, and metabolic regulation. To investigate the function and regulatory mechanism of the HtbZIP60 gene in Houttuynia cordata thunb, total RNA was extracted from Houttuynia cordata thunbas the material, and the first strand of cDNA was synthesized. Subsequently, the HtbZIP60 gene from Houttuynia cordata thunb was successfully cloned, and relevant bioinformatics analysis was conducted. The re-sults revealed that the coding sequence of HtbZIP60 is 996 bp in length, encoding 331 amino acids, with a protein molecular weight of 37447.00 ku. It lacks a signal peptide cleavage site but contains a transmembrane structure domain, predominantly composed of α-helices. The protein is localized in the cell nucleus and possesses 30 known functional promoters. These findings provide a scientific foundation for further exploring the biological functions of HtbZIP60 in the growth and development of Houttuynia cordata thunb.

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