|Table of Contents|

Cloning and Expression Analysis of Flavanone 3-hydroxylase SlF3H-like Gene From Purple Tomato

《北方园艺》[ISSN:1001-0009/CN:23-1247/S]

Issue:
2022年17
Page:
26-33
Research Field:
Publishing date:

Info

Title:
Cloning and Expression Analysis of Flavanone 3-hydroxylase SlF3H-like Gene From Purple Tomato
Author(s):
LIU Zhengjie12LIU Yuntong1XU Shaozhong1MAO Zichao12LIN Chun12
(1.College of Agriculture and Biotechnology,Yunnan Agricultural University,Kunming,Yunnan 650201;2.Institute of Improvement and Utilization of Characteristic Resource Plants,Yunnan Agricultural University,Kunming,Yunnan 650201)
Keywords:
purple tomatoSlF3H-like genecloninganthocyaninsexpression analysis
PACS:
-
DOI:
10.11937/bfyy.20220892
Abstract:
The cherry purple tomato ‘Yanzi No.1’ was used as test material.RT-PCR,bioinformatics and qRT-PCR expression analysis were used to study the biological information of flavanone 3-hydroxylase gene SlF3H-like,in order to characterize the sequence characteristics and expression pattern of the gene.The results showed that the open reading frame (ORF) of SlF3H-like gene was 1 089 bp,encoding 362 amino acids.The random coil was found to occupy the majority of structural elements of SlF3H-like protein,followed by α-helix and extended chain.The F3H amino acid sequence of ‘Yanzi No.1’ was highly conserved from other species.SlF3H-like protein contained typical DIOX-N superfamily and 2OG-FeⅡ_Oxy domains.Phylogenetic analysis showed that ‘Yanzi No.1’ was closely related to ‘Pannali’ tomato,followed by potato.The anthocyanin content in leaves and pericarp of ‘Yanzi No.1’ was measured during its development.It was found that the anthocyanin content in pericarp gradually accumulated with the increase of fruit diameter,while the anthocyanin content in leaves increased first and then decreased sharply with the increase of leaf diameter.qRT-PCR was used to analyze the expression of SlF3H-like gene in the pericarp and leaves of ‘Yanzi No.1’.Results showed that the change trend of this gene expression was similar to that of anthocyanin content,indicating that SlF3H-like gene played an important role in anthocyanin accumulation of purple tomato.

References:

[1]陈丽,王定林,王跃云,等.番茄新品种砚紫1号选育[J].辣椒杂志,2018(3):35-39.[2]张园,张婉荣,林春,等.富花青素紫色番茄组织培养再生体系的建立[J].北方园艺,2018(18):41-47.[3]张园,徐绍忠,毛自朝,等.紫色番茄SlWD40-like基因克隆与表达分析[J].西北农业学报,2019,28(4):586-593.[4]YAN S,CHEN N,HUANG Z,et al.Anthocyanin fruit encodes an R2R3-MYB transcription factor,SlAN2-like,activating the transcription of SlMYBATV to fine-tune anthocyanin content in tomato fruit[J].New Phytologist,2019,225:2048-2063.[5]许志茹,崔国新,李春雷,等.芜菁黄烷酮3-羟化酶基因的克隆、序列分析及表达[J].分子植物育种,2008,6(4):787-792.[6]FERREYRA M F,RIUS S P,CASATI P.Flavonoids:Biosynthesis,biological functions,and biotechnological applications[J].Frontiers in Plant Science,2012,3(222):1-15.[7]王海竹,闫海芳,徐启江.红穗和白穗醋栗F3H的克隆及其在果实成熟过程中的表达分析[J].园艺学报,2016,43(10):2003-2011.[8]MARTIN C,PRESCOTT A,MACKAY S.Control of anthocyanin biosynthesis in flowers of Antirrhinum majus[J].Plant Journal,1991(1):37-49.[9]BRITSCH L,RUHNAU-BRICH B,FORKMANN G.Molecular cloning,sequence analysis,and in vitro expression of flavanone 3 beta-hydroxylase from Petunia hybrid[J].Journal of Biological Chemistry,1992,267(8):5380-5387.[10]DAVIES K M.A cDNA clone for flavanone 3-hydroxylase from Malus[J].Plant Physiology,1993,103(1):291.[11]DEBOO G B,ALBERTSEN M C,TAYLOR L P.Flavanone-3-hydroxylase transcripts and flavonol accumulation are temporally coordinate in maize anthers[J].Plant Journal,1995,7(5):703-713.[12]OWENS D K,CROSBY K C,RUNAC J,et al.Biochemical and genetic characterization of Arabidopsis flavanone-3-β-hydroxylase[J].Plant Physiology and Biochemistry,2008,46(10):833-843.[13]SHEN X,MARTENS S,CHEN M,et al.Cloning and characterization of a functional flavanone-3β-hydroxylase gene from Medicago truncatula[J].Molecular Biology Reports,2010,37 (7):3283-3289.[14]LIU M,LI X,LIU Y,et al.Regulation of flavanone 3-hydroxylase gene involved in the flavonoid biosynthesis pathway in response to UV-B radiation and drought stress in the desert plant,Reaumuria soongorica[J].Plant Physiology and Biochemistry,2013,73:161-167.[15]张华玲,黄元射,杨春贤,等.苦荞黄烷酮3-羟化酶基因F3H的克隆及序列分析[J].西北植物学报,2010,30(3):447-452.[16]ZHANG Y,HU Z,CHU G,et al.Anthocyanin accumulation and molecular analysis of anthocyanin biosynthesis-associated genes in eggplant (Solanum melongena L.)[J].Journal of Agricultural and Food Chemistry,2014,62(13):2906-2912.[17]赵乐,马利刚,张金燕,等.独行菜LaF3H基因克隆、序列分析及原核表达[J].中草药,2018,49(23):5626-5632.[18]SONG X,DIAO J,JI J,et al.Molecular cloning and identification of a flavanone 3-hydroxylase gene from Lycium chinense,and its overexpression enhances drought stress in tobacco[J].Plant Physiology and Biochemistry,2016,98:89-100.[19]袁岐,张春利,赵婷婷,等.番茄GRF 转录因子家族的生物信息学分析[J].分子植物育种,2017,15(8):2949-2956.[20]孙蓉,何周凤,陈惠,等.角蛋白酶kerC基因的克隆及序列分析[J].基因组学与应用生物学,2017,36(5):1965-1970.[21]LIU W,DONG D,YANG Z,et al.Polymerase Spiral Reaction (PSR):A novel isothermal nucleic acid amplification method[J].Scientific Reports,2015(5):12723.[22]马小磊,高霞莉,叶雯青,等.甘薯茎叶中花青素的定位及含量测定[J].植物学研究,2017,6(2):31-38.[23]黄春红,高燕会,朱玉球,等.石蒜黄烷酮3-羟化酶基因LrF3H的克隆及表达分析[J].园艺学报,2013,40(5):960-970.[24]宋祥忠,黄克江,王瑞珩.白芨(Bletilla striata)黄烷酮3-羟化酶基因的克隆和表达分析[J].分子植物育种,2019,17(14):4586-4591.[25]许明,伊恒杰,郭佳鑫,等.藤茶黄烷酮3-羟化酶基因AgF3H的克隆及表达分析[J].西北植物学报,2020,40(2):185-192.[26]张佩佩,张亮,郑凤霞,等.植物叶片中花青素的积累规律及生物学作用[J].北方园艺,2014(20):188-192.

Memo

Memo:
-
Last Update: 2022-11-09