Wang L J, Sun X W, Guo F Y, Zhao Y J, Zhang J H, Zhao Z Q
Chongqing Engineering Research Center for Herbivores Resource Protection and Utilisation, Southwest University, Chongqing, China.
Reprod Domest Anim. 2016 Dec;51(6):877-885. doi: 10.1111/rda.12750. Epub 2016 Sep 20.
Transcriptome analysis of Inner Mongolia Cashmere goat and Dazu black goat generated 38,772,947 and 38,771,668 clean pair end reads, respectively, which were assembled into 72,422 and 80,069 unigenes by Trinity, respectively. For Inner Mongolia Cashmere goat, 26,051 and 10,100 unigenes were assigned to gene ontology (GO) categories and clusters of orthologous groups, respectively. A total of 32,772 unigenes can comment to SWISS-Prot database, and the Kyoto Encyclopedia of Genes and Genomes Pathway database (KEGG) mapped 24,420 unigenes. While annotating the unigenes about Dazu black goats, we found 29,444(45.42%), 11,271 (38.28%), 36,910(56.94%) and 27,766 (42.83%) unigenes were assigned to GO database, COG database, SWISS-Prot database and KEGG database, respectively. In addition, we performed the bioinformatics analysis of gene expression profiling aimed at the ovarian transcriptome difference between Inner Mongolia Cashmere goat and Dazu black goat. We obtained a sequencing depth of over 5.5 million and 5.8 million tags. There were 1,133 DEGs between two species, of which 632 genes upregulated in the Dazu black goat and 501 genes downregulated compared with which in Inner Mongolia Cashmere goat. By annotating the 1,133 DEGs into KEGG database, we found 525 DEGs. And there were 68 DEGs annotated in metabolic pathways, 31 DEGs annotated in ribosome, 28 DEGs annotated in focal adhesion, 27 DEGs annotated in phagosome, 26 DEGs annotated in pathways in cancer, 25 DEGs annotated in ECM-receptor interaction, 23 DEGs annotated in protein digestion and absorption, 20 DEGs annotated in oxidative phosphorylation, 17 DEGs annotated in lysosome, and 16 DEGs annotated in cell adhesion molecules.
对内蒙古绒山羊和大足黑山羊的转录组分析分别产生了38,772,947和38,771,668条干净的双端 reads,通过Trinity分别组装成了72,422和80,069个单基因。对于内蒙古绒山羊,分别有26,051和10,100个单基因被归类到基因本体论(GO)类别和直系同源基因簇中。共有32,772个单基因可注释到SWISS-Prot数据库,京都基因与基因组百科全书通路数据库(KEGG)映射到24,420个单基因。在注释大足黑山羊的单基因时,我们发现分别有29,444(45.42%)、11,271(38.28%)、36,910(56.94%)和27,766(42.83%)个单基因被分配到GO数据库、COG数据库、SWISS-Prot数据库和KEGG数据库。此外,我们针对内蒙古绒山羊和大足黑山羊卵巢转录组差异进行了基因表达谱的生物信息学分析。我们获得了超过550万和580万标签的测序深度。两个物种之间有1,133个差异表达基因(DEG),其中与内蒙古绒山羊相比,大足黑山羊中有632个基因上调,501个基因下调。通过将这1,133个DEG注释到KEGG数据库中,我们发现了525个DEG。并且有68个DEG注释在代谢途径中,31个DEG注释在核糖体中,28个DEG注释在粘着斑中,27个DEG注释在吞噬体中,26个DEG注释在癌症通路中,25个DEG注释在细胞外基质受体相互作用中,23个DEG注释在蛋白质消化和吸收中,20个DEG注释在氧化磷酸化中,17个DEG注释在溶酶体中,16个DEG注释在细胞粘附分子中。