基因组学与应用生物学
基因組學與應用生物學
기인조학여응용생물학
Genomics and Applied Biology
2012年
2期
147-153
,共7页
刘朋虎%邓优锦%江玉姬%谢宝贵%王海英%章小寅
劉朋虎%鄧優錦%江玉姬%謝寶貴%王海英%章小寅
류붕호%산우금%강옥희%사보귀%왕해영%장소인
草菇%子实体形成%数字基因表达谱%差异表达基因
草菇%子實體形成%數字基因錶達譜%差異錶達基因
초고%자실체형성%수자기인표체보%차이표체기인
Fruit body formation%Volvariella volvacea%Digital gene expression profiling%Differentially expressed gene
采用Solexa测序技术,对草菇菌丝体和原基进行了数字基因表达谱(DGE)测序,在菌丝体和原基文库中分别得到5701781个和5659262个高质量测序标签(cleantags),对应的标签种数(distinct clean tags)分别为85626和95363。将所有高质量测序标签与参考基因库进行比对,在菌丝体和原基文库中,占标签种数的43.32%和52.57%的标签可以唯一定位(map)到参考序列上,占标签种数的21.65%和21.47%的标签可以被定位到基因组序列上。最终,被菌丝体和原基标签唯一定位的基因数(unambiguous tag-mapped genes)分别为14794和15534。差异基因分析显示,两个文库中共有显著性差异表达的基因4163个,其中在原基中上调、下调的基因数分别为2486和1677,只在原基中表达的基因321个。经过Blastnr比对,在原基中特异表达的基因,涉及蛋白质(氨基酸)合成与代谢、糖代谢、脂类代谢和抗逆反应等多个代谢途径。GO功能富集分析结果表明,葡萄糖、己糖和乙醇等代谢途径大部分基因下调表达。Pathway功能富集分析结果表明,合成核糖体蛋白的基因均下调表达,表明原基形成时细胞代谢减弱,蛋白质合成量减小。
採用Solexa測序技術,對草菇菌絲體和原基進行瞭數字基因錶達譜(DGE)測序,在菌絲體和原基文庫中分彆得到5701781箇和5659262箇高質量測序標籤(cleantags),對應的標籤種數(distinct clean tags)分彆為85626和95363。將所有高質量測序標籤與參攷基因庫進行比對,在菌絲體和原基文庫中,佔標籤種數的43.32%和52.57%的標籤可以唯一定位(map)到參攷序列上,佔標籤種數的21.65%和21.47%的標籤可以被定位到基因組序列上。最終,被菌絲體和原基標籤唯一定位的基因數(unambiguous tag-mapped genes)分彆為14794和15534。差異基因分析顯示,兩箇文庫中共有顯著性差異錶達的基因4163箇,其中在原基中上調、下調的基因數分彆為2486和1677,隻在原基中錶達的基因321箇。經過Blastnr比對,在原基中特異錶達的基因,涉及蛋白質(氨基痠)閤成與代謝、糖代謝、脂類代謝和抗逆反應等多箇代謝途徑。GO功能富集分析結果錶明,葡萄糖、己糖和乙醇等代謝途徑大部分基因下調錶達。Pathway功能富集分析結果錶明,閤成覈糖體蛋白的基因均下調錶達,錶明原基形成時細胞代謝減弱,蛋白質閤成量減小。
채용Solexa측서기술,대초고균사체화원기진행료수자기인표체보(DGE)측서,재균사체화원기문고중분별득도5701781개화5659262개고질량측서표첨(cleantags),대응적표첨충수(distinct clean tags)분별위85626화95363。장소유고질량측서표첨여삼고기인고진행비대,재균사체화원기문고중,점표첨충수적43.32%화52.57%적표첨가이유일정위(map)도삼고서렬상,점표첨충수적21.65%화21.47%적표첨가이피정위도기인조서렬상。최종,피균사체화원기표첨유일정위적기인수(unambiguous tag-mapped genes)분별위14794화15534。차이기인분석현시,량개문고중공유현저성차이표체적기인4163개,기중재원기중상조、하조적기인수분별위2486화1677,지재원기중표체적기인321개。경과Blastnr비대,재원기중특이표체적기인,섭급단백질(안기산)합성여대사、당대사、지류대사화항역반응등다개대사도경。GO공능부집분석결과표명,포도당、기당화을순등대사도경대부분기인하조표체。Pathway공능부집분석결과표명,합성핵당체단백적기인균하조표체,표명원기형성시세포대사감약,단백질합성량감소。
The expression profiling of mycelium and primordium of Volvariella volvacea was analyzed by using high-throughput sequencing technology based on the Solexa Genome Analyzer platform.Totally 5 701 781 and 5 659 262 clean tags for mycelium and primordium libraries were obtained corresponding to 85 626 and 95 363 distinct clean tags respectively.Comparing all the clean tags with gene bank,in mycelium and primordium libraries,43.32% and 52.27% of the distinct clean tags were mapped unambiguously to the reference database respectively,and 21.65% and 21.74% of the distinct clean tags were mapped to the genome database of Volvariella volvacea.Finally,14 794 and 15 534 unambiguous tag-mapped genes were obtained.Analysis of differentially expressed genes shows that there are 4 163 genes differentially expressed between two libraries,and in the primordium library,2 486 of them are up-regulated while 1 677 of them are down-regulated.There are 321 genes that are only expressed in the primordium library.With Blastnr comparison,they are found to be related to protein and amino metabolism,glucose metabolism,lignin and cellulose degradation,lipid metabolism cytoskeleton,and so on.Gene ontology functional enrichment analysis reveals that most genes related to glucose metabolic process,monosaccharide catabolic process,hexose catabolic process,alcohol catabolic process,and glucose metabolic process are down-regulated.Pathway enrichment analysis shows that genes related to ribosome are all down-regulated,and this indicates that when primordium is developed the cell metabolism slows down and the protein synthesis decreases.