药用猪苓菌核9种主要协助转运蛋白超家族基因的克隆与表达分析

刘蒙蒙, 邢咏梅, 郭顺星

中国药学杂志 ›› 2017, Vol. 52 ›› Issue (10) : 819-824.

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中国药学杂志 ›› 2017, Vol. 52 ›› Issue (10) : 819-824. DOI: 10.11669/cpj.2017.10.004
论著

药用猪苓菌核9种主要协助转运蛋白超家族基因的克隆与表达分析

  • 刘蒙蒙1,2, 邢咏梅1, 郭顺星1*
作者信息 +

Cloning and Expression Analysis of Nine Major Facilitator Superfamily Encoding Genes in Polyporus umbellatus

  • LIU Meng-meng1,2, XING Yong-mei1, GUO Shun-xing1*
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文章历史 +

摘要

目的 克隆分离药用真菌猪苓菌核的主要协助转运蛋白超家族基因并进行生物信息学分析。方法 采用 RT-PCR技术从中国野生猪苓菌核(Polyporus umbellatus)中克隆得到 9个主要协助转运蛋白超家族(major facilitator superfamily,MFS)基因,利用生物信息学方法分析这9个基因的特点,并利用qPCR验证这9个基因在不同猪苓菌核部分的表达情况。结果 该9个基因 cDNA包含的完整开放阅读框在1 321~1 860 bp之间,编码的氨基酸的数量在441~620之间,相对分子质量在(48.45~64.79)×103之间,理论等电点在6.59~9.56之间。氨基酸序列分析表明,这9个基因编码的主要协助转运蛋白的跨膜区在11~14之间。氨基酸序列多重比对及系统发育树结果显示,Comp34750Comp34832Comp29252Comp42895Comp32579Comp27555与MFS general substrate transporter同源性比较高,Comp28872Comp26306与MFS单糖转运蛋白(MFS monosaccharide transporter)同源性比较高,Comp33117与MFS糖转运蛋白(MFS sugar transporter)同源性比较高。实时荧光定量 RT-PCR 分析表明,这9个基因在不同的菌核部分都有表达,除基因Comp34382Comp32579在共生部位显著下调外,其他7个基因都是表达显著上调。结论 提示这些基因可能以不同方式参与了猪苓的防御反应及吸收外界营养元素的过程。

Abstract

OBJECTIVE To clone and isolate the major facilitator superfamily(MFS)genes of Polyporus umbellatus and carry out bioinformatic analysis. METHODS Nine major facilitator superfamily(MFS)genes were cloned from Polyporus umbellatus sclerotia by RT-PCR and the expression analysis of the nine genes in different parts of Polyporus umbellatus sclerotia was carried out using quantitative Real-time PCR.RESULTS The full open reading frame cDNA sequence of these nine genes was between 1 321 and 1 860 bp, the putative encoding proteins were between 441 and 620 amino acids, the molecular weight was between 48.45×103 and 64.79×103 and the theoretical pI was between 6.59 and 9.56. The amino acids of these nine genes possessed 11 to 14 membrane-spanning domains. Phylogenetic tree analysis indicated that Comp34750,Comp34832, Comp29252, Comp42895, Comp32579 and Comp27555 had the highest similarity with MFS general substrate transporter,Comp28872 and Comp26306 had the highest similarity with MFS monosaccharide transporter, and Comp33117 had the highest similarity with MFS sugar transporter. Quantitative real-time PCR showed that these nine genes were expressed in both the symbiotic part and non-symbiotic part. Meanwhile,the expressions of seven genes were significantly up-regulated in the symbiotic part except Comp34382 and Comp32579. CONCLUSION The investigated nine genes might play an important role during the defense response and nutrient absorption of P.umbellatus.

关键词

猪苓 / 主要协助转运蛋白超家族 / 基因克隆 / 表达分析

Key words

Polyporus umbellatus / major facilitator superfamily / gene clone / expression analysis

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刘蒙蒙, 邢咏梅, 郭顺星. 药用猪苓菌核9种主要协助转运蛋白超家族基因的克隆与表达分析[J]. 中国药学杂志, 2017, 52(10): 819-824 https://doi.org/10.11669/cpj.2017.10.004
LIU Meng-meng, XING Yong-mei, GUO Shun-xing. Cloning and Expression Analysis of Nine Major Facilitator Superfamily Encoding Genes in Polyporus umbellatus[J]. Chinese Pharmaceutical Journal, 2017, 52(10): 819-824 https://doi.org/10.11669/cpj.2017.10.004
中图分类号: R965   

参考文献

[1] MITCHELL P. Translocations through natural membranes [J]. Adv Enzymol Relat Areas Mol Biol, 1967, 29(29):33-87.
[2] PAULSEN I T, SLIWINSKI M K, SAIER M H. Microbial genome analyses:global comparisons of transport capabilities based on phylogenies, bioenergetics and substrate specificities [J]. J Mol Biol, 1998, 277(3):573-592.
[3] HENDERSON P, MAIDEN M. Homologous sugar transport proteins in Escherichia coli and their relatives in both prokaryotes and eukaryotes [J]. Philos Trans R Soc Lond B:Biol Sci, 1990, 326(1236):391-410.
[4] GRIFFITH J K, BAKER M E, ROUCH D A, et al. Membrane transport proteins:implications of sequence comparisons [J]. Curr Opin Cell Biol, 1992, 4(4):684-695.
[5] MARGER M D, SAIER M H. A major superfamily of transmembrane facilitators that catalyse uniport, symport and antiport [J]. Trends Biochem Sci, 1993, 18(1):13-20.
[6] REIZER J, REIZER A, SAIER M H. A functional superfamily of sodium/solute symporters [J]. Biochim Biophys Acta, 1994, 1197(2):133-166.
[7] CRUTCHER F K, LIU J, PUCKHABER L S, et al. FUBT, a putative MFS transporter, promotes secretion of fusaric acid in the cotton pathogen Fusarium oxysporum f. sp. vasinfectum [J]. Microbiology, 2015, 161(Pt 4):875-883.
[8] KHAOKHAJORN P, SAMIPAK S, NITHITHANASILP S, et al. Production and secretion of naphthoquinones is mediated by the MFS transporter MFS1 in the entomopathogenic fungus Ophiocordyceps sp. BCC1869 [J]. World J Microbiol Biotechnol, 2015,31(10):1543-1554.
[9] SAIER M H. Genome archeology leading to the characterization and classification of transport proteins [J]. Curr Opin Microbiol, 1999, 2(5):555-561.
[10] SAIER M H. Tracing pathways of transport protein evolution [J]. Mol Microbiology, 2003, 48(5):1145-1156.

基金

国家重点基础研究发展计划资助项目(2014CB13830X);2014年度山西省煤基重点科技攻关项目资助项目(FT2014-03);河北山区特色中药材种质资源评价与仿野生栽培技术研究与示范资助项目(16232503D)
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