机构地区:[1]江苏省中国科学院植物研究所(南京中山植物园),江苏南京210014
出 处:《植物资源与环境学报》2021年第3期8-19,共12页Journal of Plant Resources and Environment
基 金:江苏省植物资源研究与利用重点实验室基金项目(SQ201404);省属公益类科研院所自主科研项目(BM2018021-2)。
摘 要:以薯蓣(Dioscorea polystachya Turcz.)的具茎生珠芽品种‘铁棍山药’(‘Tiegun’)和无茎生珠芽品种‘花籽山药’(‘Huazi’)为研究对象,采集‘铁棍山药’具茎生珠芽、茎基部无茎生珠芽和茎上部无茎生珠芽的叶腋部位以及‘花籽山药’的叶腋部位4组样品进行转录组测序,并以‘铁棍山药’不同发育期茎生珠芽的叶腋部位为样品进行qRT-PCR分析,以期明确与薯蓣茎生珠芽发生相关的调控基因。结果显示:从2个品种不同部位的4组样品中共获得77981个All-unigenes,长度主要集中于300~3000 bp,占总量的99.44%;All-unigenes的平均长度为1050 bp,N50值为1764 bp,GC含量为42.66%;转录组unigenes与油棕(Elaeis guineensis Jacq.)和海枣(Phoenix dactylifera Linn.)的同源性较高。对具茎生珠芽叶腋样品与3组无茎生珠芽叶腋样品的差异unigenes进行功能注释和表达量比较。结果显示:经过GO注释分析,3组转录组分别有6098、8840和9141个差异unigenes注释在细胞组分、分子功能和生物过程3大类43个亚类中,其中,注释在代谢过程亚类的差异unigenes数分别占对应注释unigenes总数的10.6%、10.5%和10.7%;3组转录组分别有11182、13552和15918个差异unigenes注释在KEGG代谢通路,且主要集中在代谢和遗传信息处理;表达量均上调的unigenes有3531个,表达量均下调的unigenes有1084个;在具茎生珠芽叶腋部位中特异性表达的unigenes有235个,而在无茎生珠芽叶腋部位中均特异性表达的unigene仅1个。从转录组中共鉴定出11个PEBP家族成员,且在系统演化树上这些PEBP家族基因主要分布在TFL 1-like和FT-like分支上,其中位于TFL 1-like分支的Unigene40804_All与拟南芥〔Arabidopsis thaliana(Linn.)Heynh.〕中已知功能的TFL 1基因高度同源,被命名为DpTFL 1,且DpTFL 1基因仅在‘铁棍山药’具茎生珠芽的叶腋部位表达。qRT-PCR分析结果显示:随‘铁棍山药’茎生珠芽发育,DpTFL 1基因的表达量逐�Taking cultivar‘Tiegun’(with stem bulbils)and‘Huazi’(without stem bulbil)of Dioscorea polystachya Turcz.as research objects,transcriptome sequencing was performed for 4 groups of samples namely leaf axils of‘Tiegun’with stem bulbils,without stem bulbil on base part of stem,and without stem bulbil on upper part of stem,and leaf axils of‘Huazi’,and qRT-PCR analysis was conducted using the leaf axils of stem bulbils of‘Tiegun’at different development stages as samples to clarify the regulation genes related to the stem bulbil genesis of D.polystachya.The results show that 77981 All-unigenes are obtained in total from 4 groups of samples from different parts of 2 cultivars,and their length are mainly concentrated within 300-3000 bp,accounting for 99.44%of the total amount;the average length of All-unigenes is 1050 bp,the N50 value is 1764 bp,and the GC content is 42.66%;the unigenes in transcriptome are highly homologous to Elaeis guineensis Jacq.and Phoenix dactylifera Linn.Functional annotation and expression comparison were conducted for differential unigenes between leaf axil sample with stem bulbils and 3 groups of leaf axil samples without stem bulbil.The results show that after GO annotation analysis,6098,8840,and 9141 differential unigenes in 3 groups of transcriptomes are annotated into 43 subcategories of 3 categories(cellular component,molecular function,and biological process),in which,the number of unigenes annotated in subcategory of metabolic process accounts for 10.6%,10.5%,and 10.7%of total number of corresponding annotated unigenes,respectively;there are 11182,13552,and 15918 differential unigenes in 3 groups of transcriptomes annotated in KEGG metabolic pathway,and are mainly concentrated in metabolism and genetic information processing;the number of up-regulated unigenes is 3531,and that of down-regulated unigenes is 1084;there are 235 specifically expressed unigenes in leaf axils with stem bulbils,while there is only 1 unigene specifically expressed in all leaf axils without s
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