白鸡冠茶树CsPPH基因全长cDNA克隆与表达分析

doi:10.13305/j.cnki.jts.20200117.007

茶叶科学 ›› 2020, Vol. 40 ›› Issue (1): 39-50.doi: 10.13305/j.cnki.jts.20200117.007

白鸡冠茶树CsPPH基因全长cDNA克隆与表达分析

周喆^1,2,4, 陈志丹^2,3,4, 吴全金⁵, 徐一岚³, 孙威江^1,2,3,4,*

1. 福建农林大学园艺学院,福建福州 350002;
2. 安溪县现代农业产业协同创新中心,福建泉州 362400;
3. 福建农林大学安溪茶学院,福建泉州 362400;
4. 福建省茶叶工程技术研究中心,福建福州 350002;
5. 福建广播电视大学财经与管理系,福建福州 350002

收稿日期:2019-06-10 修回日期:2019-09-02 出版日期:2020-02-15 发布日期:2020-02-04
通讯作者: *swj8103@126.com
作者简介:周喆，女，硕士研究生，主要从事茶树栽培育种与分子生物学方面的研究，742382124@qq.com。
基金资助:
国家自然科学基金项目（31770732）、农业农村部资助项目——福建省安溪县现代农业产业园建设（KMD18003A）、2017年福建省科技计划项目（2017N3012）

Cloning and Expression Analysis of CsPPH Gene in Tea Plant (Camellia sinensis)

ZHOU Zhe^1,2,4, CHEN Zhidan^2,3,4, WU Quanjin⁵, XU Yilan³, SUN Weijiang^1,2,3,4,*

1. College of Horticulture, Fujian Agriculture and Forestry University, Fuzhou 350002, China;
2. Collaborative Innovation Center of Modern Agriculture Industrial Park of Anxi County, Quanzhou 362400, China;
3. College of Tea, Fujian Agriculture and Forestry University, Quanzhou 362400, China;
4. Engineering Technology and Research Center of Fujian Tea Industry, Fuzhou 350002, China;
5. Department of Finance and Management, The Open University of Fujian, Fuzhou 350002, China

Received:2019-06-10 Revised:2019-09-02 Online:2020-02-15 Published:2020-02-04

摘要/Abstract

摘要： 脱镁叶绿素酶（Pheophytinase,PPH）是叶绿素降解过程中的一个关键酶,它能使脱镁叶绿素a转化为脱镁叶绿酸a,脱镁叶绿酸a是叶绿素降解途径中最后一个保持植物绿色的产物,被认为是叶片衰老和黄化的关键步骤。以新梢白化茶树白鸡冠叶片为材料,克隆获得CsPPH基因cDNA的全长序列（登录号：MK359094）,并对其进行生物信息学分析。结果表明,CsPPH全长为1 298 bp,包含的ORF序列为1 241 bp,编码413个氨基酸。序列分析表明,该基因编码的蛋白质为稳定疏水蛋白,其预测分子量为45 741.50 Da,理论等电点为6.12。预测该基因主要定位于叶绿体中。qRT-PCR结果显示,遮荫抑制白鸡冠叶片CsPPH的表达,叶绿素升高,叶色变绿;光照促进白鸡冠叶片CsPPH的表达,叶绿素降解,导致叶片白化。

关键词: 茶树白化, PPH基因, 克隆, 生物信息学分析

Abstract: Pheophytinase (PPH) is a key enzyme in chlorophyll degradation. It can convert pheophytin a into pheophorbide a, which is the last product to keep green in chlorophyll degradation pathway. This step is considered to be a key step of leaf senescence and yellowing. In this study, the full-length sequence of CsPPH gene was cloned from the new shoot leaves of albino tea plant Camellia sinensis cv. Baijiguan (MK359094), and its biological characteristics were analyzed. The full-length of CsPPH was 1 298 bp, and the ORF was 1 241 bp, encoding 413 amino acids. Sequence analysis indicated that the encoded protein was a stable hydrophobic protein, and its molecular weight was predicted to be 45 741.50 Da. Its theoretical isoelectric point was 6.12. It was mainly located in chloroplasts. The real-time fluorescence quantitative PCR showed that under shading conditions, the expression of CsPPH was inhibited, chlorophyll increased and leaf color turned green. Light promoted the expression of CsPPH in leaves of cv. Baijiguan, and chlorophyll degradation led to leaf albinism.

Key words: albinism of tea plant, PPH gene, clone, bioinformatics analysis

中图分类号:

S571.1
Q52

周喆, 陈志丹, 吴全金, 徐一岚, 孙威江. 白鸡冠茶树CsPPH基因全长cDNA克隆与表达分析[J]. 茶叶科学, 2020, 40(1): 39-50. doi: 10.13305/j.cnki.jts.20200117.007.

ZHOU Zhe, CHEN Zhidan, WU Quanjin, XU Yilan, SUN Weijiang. Cloning and Expression Analysis of CsPPH Gene in Tea Plant (Camellia sinensis)[J]. Journal of Tea Science, 2020, 40(1): 39-50. doi: 10.13305/j.cnki.jts.20200117.007.

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白鸡冠茶树CsPPH基因全长cDNA克隆与表达分析

Cloning and Expression Analysis of CsPPH Gene in Tea Plant (Camellia sinensis)

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