浙江农业学报
浙江農業學報
절강농업학보
ACTA AGRICULTURAE ZHEJIANGENSIS
2013年
6期
1220-1224
,共5页
路伏增%褚晓红%戴丽荷%陈绍孟%傅春泉%胡锦平%徐如海
路伏增%褚曉紅%戴麗荷%陳紹孟%傅春泉%鬍錦平%徐如海
로복증%저효홍%대려하%진소맹%부춘천%호금평%서여해
MUC13%仔猪腹泻%调控网络
MUC13%仔豬腹瀉%調控網絡
MUC13%자저복사%조공망락
MUC13%piglet diarrhea%regulation network
为进一步阐述仔猪腹泻发生的分子机制,应用生物信息学方法构建了MUC13基因参与的仔猪腹泻调控网络图谱,并对其中的基因进行基因功能聚类分析。首先,选择物种为猪,通过STRING 数据库分析发现与MUC13相关联的有10种蛋白(MUC4,MUC20,LRCH3,FLJ33471,ACK,ZDHHC19,CTPCT,APOD,Msp, CD71);其次,根据筛选到的蛋白,构建了仔猪腹泻调控网络,并从中找到了MUC13基因参与的仔猪腹泻调控网络,该网络包括MUC13,MUC4,MUC1,MUC2,MUC3,TFF3,NOD1,TNFSF10,FGFR1,CDH2等10个基因;最后,采用DAVID数据库对图谱中的这10个基因进行基因功能注释分析,发现富集相关程度较高的一些基因聚类条目有上皮生长因子( EGF)序列、SEA模块、跨膜结构域、胞质尾区等,因此推测MUC13基因结构的特异性决定了其在仔猪腹泻发展过程中具有特定的功能。文章建立的MUC13基因参与的仔猪腹泻调控网络具有一定的真实性,可以用来描述仔猪腹泻症发生发展过程中分子的相互作用。
為進一步闡述仔豬腹瀉髮生的分子機製,應用生物信息學方法構建瞭MUC13基因參與的仔豬腹瀉調控網絡圖譜,併對其中的基因進行基因功能聚類分析。首先,選擇物種為豬,通過STRING 數據庫分析髮現與MUC13相關聯的有10種蛋白(MUC4,MUC20,LRCH3,FLJ33471,ACK,ZDHHC19,CTPCT,APOD,Msp, CD71);其次,根據篩選到的蛋白,構建瞭仔豬腹瀉調控網絡,併從中找到瞭MUC13基因參與的仔豬腹瀉調控網絡,該網絡包括MUC13,MUC4,MUC1,MUC2,MUC3,TFF3,NOD1,TNFSF10,FGFR1,CDH2等10箇基因;最後,採用DAVID數據庫對圖譜中的這10箇基因進行基因功能註釋分析,髮現富集相關程度較高的一些基因聚類條目有上皮生長因子( EGF)序列、SEA模塊、跨膜結構域、胞質尾區等,因此推測MUC13基因結構的特異性決定瞭其在仔豬腹瀉髮展過程中具有特定的功能。文章建立的MUC13基因參與的仔豬腹瀉調控網絡具有一定的真實性,可以用來描述仔豬腹瀉癥髮生髮展過程中分子的相互作用。
위진일보천술자저복사발생적분자궤제,응용생물신식학방법구건료MUC13기인삼여적자저복사조공망락도보,병대기중적기인진행기인공능취류분석。수선,선택물충위저,통과STRING 수거고분석발현여MUC13상관련적유10충단백(MUC4,MUC20,LRCH3,FLJ33471,ACK,ZDHHC19,CTPCT,APOD,Msp, CD71);기차,근거사선도적단백,구건료자저복사조공망락,병종중조도료MUC13기인삼여적자저복사조공망락,해망락포괄MUC13,MUC4,MUC1,MUC2,MUC3,TFF3,NOD1,TNFSF10,FGFR1,CDH2등10개기인;최후,채용DAVID수거고대도보중적저10개기인진행기인공능주석분석,발현부집상관정도교고적일사기인취류조목유상피생장인자( EGF)서렬、SEA모괴、과막결구역、포질미구등,인차추측MUC13기인결구적특이성결정료기재자저복사발전과정중구유특정적공능。문장건립적MUC13기인삼여적자저복사조공망락구유일정적진실성,가이용래묘술자저복사증발생발전과정중분자적상호작용。
This study developed a regulation network of piglets diarrhea in which MUC13 gene participated and made an assay of gene functional annotation clustering .Firstly, 10 MUC13-associated proteins were generated through STRING 9.0 (MUC4, MUC20, LRCH3, FLJ33471, ACK, ZDHHC19, CTPCT, APOD, Msp, CD71).Secondly, using the 10 MUC13-associated proteins , we developed a regulation network of piglets diarrhea in which MUC13 gene participated, which included MUC13, MUC4, MUC1, MUC2, MUC3, TFF3, NOD1, TNFSF10, FGFR1, CDH2 genes.Finally, with DAVID bioinformatics resources , we made an assay of gene functional annotation clustering , and found specific functional annotations terms included domain:SEA, extracellular region , transmembrane protein , so we speculated that the specific structure of the MUC13 determined MUC13 had a specific function in the develop-ment process of piglet diarrhea .The network constructed in this study has certain authenticity and can be used for de-scribing molecular interactions in the occurrence and development of piglet diarrhea , which is important to elucidate the molecular mechanisms of diarrhea occurrence .