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光皮桦转录组及S-腺苷甲硫氨酸合成酶基因分析

倪飞 励文豪 蔡苗苗 林二培 童再康 黄华宏

农业生物技术学报2018,Vol.26Issue(3):410-420,11.
农业生物技术学报2018,Vol.26Issue(3):410-420,11.DOI:10.3969/j.issn.1674-7968.2018.03.006

光皮桦转录组及S-腺苷甲硫氨酸合成酶基因分析

Analysis of Transcriptome and the S-adenosylmethionine Synthetase (SAMS) Genes in Betula luminifera

倪飞 1励文豪 1蔡苗苗 1林二培 1童再康 1黄华宏1

作者信息

  • 1. 浙江农林大学亚热带森林培育国家重点实验室,临安311300
  • 折叠

摘要

Abstract

Transcriptome sequencing is a rapid and efficient way to obtain gene expression information.Betula luminifera is one of the superior woody species in China.In order to excavate the genes involved in its wood formation,the transcriptome sequencing,sequencing data assembly,and functional annotation and classification of the sequences were conducted by using the stems and leaves as materials in this study.Then the full-length cDNAs of S-adenosylmethionine synthase (SAMS) gene were isolated by RACE technique.The sequence feature and phylogenetic tree were analyzed by using bioinformatics software,such as DNAStar,MAGA7.0,and the expression pattern was detected by fluorescence quantitative RCR.The results showed that a total of 1.9 Gbp sequencing data was obtained,and were assembled into 54 577 Unigenes.By BLAST comparison against the NR (non-redundant protein database) and the Swiss-Prot protein sequence database,65.8% (35 920) of Unigenes were annotated,which corresponded to 24 482 Unique protein accessions.Among these annotated Unigenes,7 954 and 9 997 were assigned to Gene Ontology (GO) classes and Clusters of Orthologous Groups (COG),respectively.Based on transcriptomes sequencing,BlSAMS1,BlSAMS2 and BlSAMS3 were cloned,with the cDNA length of 1 578 bp,1 555 bp and 1 266 bp,respectively.The molecular weights of the corresponding encoded proteins were 42.9,43.1 and 42.7 kD,each of which contained typical conservative domains of SAMS protein.Phylogenetic tree showed that BlSAMS1 was grouped with Catharanthus roseus SAMS2,and BlSAMS2,Malus xiaojinensis SAMS,and Vitis vinifera SAMS4 were in the same clade.BlSAMS3 was clustered into a clade with Arabidopsis thaliana SAMS3 and Pinus pinaster SAMS1,which were involved in lignin biosynthesis.The expression levels of BlSAMS1 were relatively high in leaf samples.The BlSAMS2 and BlSAMS3 were predominantly expressed in stem and xylem,and their expression levels in stem increased as the lignification progressed.It could be speculated that the BlSAMS3 played an important role in lignin biosynthesis of B.luminifera wood.Transcriptome information and the BlSAMSs expression patterns could lay a foundation for further dissection on the molecular mechanism of B.luminifera wood formation.

关键词

光皮桦/转录组测序/S-腺苷甲硫氨酸合成酶(SAMS)/基因表达

Key words

Betula luminifera/Transcriptome sequencing/S-adenosylmethionine synthetase/Gene expression

分类

农业科技

引用本文复制引用

倪飞,励文豪,蔡苗苗,林二培,童再康,黄华宏..光皮桦转录组及S-腺苷甲硫氨酸合成酶基因分析[J].农业生物技术学报,2018,26(3):410-420,11.

基金项目

国家自然科学基金项目(No.31470674)和浙江省农业新品种选育专项(No.2016C02056-2) (No.31470674)

农业生物技术学报

OA北大核心CSCDCSTPCD

1674-7968

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