中国比较医学杂志
中國比較醫學雜誌
중국비교의학잡지
CHINESE JOURNAL OF COMPARATIVE MEDICINE
2014年
4期
51-56
,共6页
刘月环%毛栋森%吴旧生%钟宇森%周莎桑%金晓音%柯贤福%应华忠
劉月環%毛棟森%吳舊生%鐘宇森%週莎桑%金曉音%柯賢福%應華忠
류월배%모동삼%오구생%종우삼%주사상%금효음%가현복%응화충
长爪沙鼠%高脂血症%二代测序技术%转录组%代谢性炎症通路
長爪沙鼠%高脂血癥%二代測序技術%轉錄組%代謝性炎癥通路
장조사서%고지혈증%이대측서기술%전록조%대사성염증통로
Mongolian gerbil%Hyperlipidemia%RNA-Seq%Ttranscriptome%Metabolic/inflammatory pathways
目的:研究饮食诱发的高脂血症长爪沙鼠模型的关键基因及代谢性炎症通路调控网络。方法利用RNA-Seq测序技术及生物信息学技术对正常组与模型组两个RNA池进行测序和分析。结果 De novo拼接后获得有效长爪沙鼠基因47522个(即≥100 bp的unigene),大小26.9 Mb,与GenBank中现有的基因比对结果表明,约82.53%的序列与基因组上的外显子序列同源;诱发高脂血症动物与正常动物之间共获得21125个差异基因,其中16087个下调,5038个上调,模型组相对于正常组存在显著的下调关系( P<0.01)。其中与长爪沙鼠高脂血症代谢性炎症密切相关的通路有8个(P<0.01),这8个通路所表达的基因中有15个与免疫和炎症相关的基因显著下调( P<0.01)。结论 RNA-Seq测序和生物信息技术可作为研究高脂血症动物模型的整体基因转录的工具,筛选出的关键基因和通路可作为研究的候选基因或操作靶点。
目的:研究飲食誘髮的高脂血癥長爪沙鼠模型的關鍵基因及代謝性炎癥通路調控網絡。方法利用RNA-Seq測序技術及生物信息學技術對正常組與模型組兩箇RNA池進行測序和分析。結果 De novo拼接後穫得有效長爪沙鼠基因47522箇(即≥100 bp的unigene),大小26.9 Mb,與GenBank中現有的基因比對結果錶明,約82.53%的序列與基因組上的外顯子序列同源;誘髮高脂血癥動物與正常動物之間共穫得21125箇差異基因,其中16087箇下調,5038箇上調,模型組相對于正常組存在顯著的下調關繫( P<0.01)。其中與長爪沙鼠高脂血癥代謝性炎癥密切相關的通路有8箇(P<0.01),這8箇通路所錶達的基因中有15箇與免疫和炎癥相關的基因顯著下調( P<0.01)。結論 RNA-Seq測序和生物信息技術可作為研究高脂血癥動物模型的整體基因轉錄的工具,篩選齣的關鍵基因和通路可作為研究的候選基因或操作靶點。
목적:연구음식유발적고지혈증장조사서모형적관건기인급대사성염증통로조공망락。방법이용RNA-Seq측서기술급생물신식학기술대정상조여모형조량개RNA지진행측서화분석。결과 De novo병접후획득유효장조사서기인47522개(즉≥100 bp적unigene),대소26.9 Mb,여GenBank중현유적기인비대결과표명,약82.53%적서렬여기인조상적외현자서렬동원;유발고지혈증동물여정상동물지간공획득21125개차이기인,기중16087개하조,5038개상조,모형조상대우정상조존재현저적하조관계( P<0.01)。기중여장조사서고지혈증대사성염증밀절상관적통로유8개(P<0.01),저8개통로소표체적기인중유15개여면역화염증상관적기인현저하조( P<0.01)。결론 RNA-Seq측서화생물신식기술가작위연구고지혈증동물모형적정체기인전록적공구,사선출적관건기인화통로가작위연구적후선기인혹조작파점。
Objective To understand some key genes and metabolic/inflammatory pathways triggered by high fat/high cholesterol ( HF/HC ) diet-induced hyperlipidemia in Mongolian gerbil .Methods Sixty 90-day-old Mongolian gerbils (including both sexes) were used in this study.The gerbils were divided into normal group (n=30, control diets) and model group (n=30, Hf/HC diets).Hyperlipidemia was induced for 4 weeks.To extract mRNA for transcriptome by RNA-Seq deep sequencing and bioinformatics .Results The results showed that 47 522 de novo gerbil genes (≥100 bp unigene ) were obtained , with a total of 26.9 Mb, and about 82.53% sequence was homologous with the exon in the common genome bases .There were 21 125 differential genes between the hyperlipidemia gerbil and normal gerbil groups , including 16 087 down-regulated and 5038 up-regulated genes .There was a significant trend of downregulation compared with the normal group ( P <0.01 ) .There were eight pathways significantly related to the metabolic inflammation in hyperlipidemia ( P<0.01) , and among the expressed genes of these pathways , 15 immune-and inflammation-related genes were significantly down-regulated ( P<0.01 ) .Conclusions RNA-Seq and bioinformatics techniques can be used as a powerful tool for overall gene-transcription in hyperlipidemic gerbil models .Some key genes and pathways screened in this study may become candidate genes or operating targets in the future research .