Lv Jie, Liu Hui, Yu Shihuan, Liu Hongbo, Cui Wei, Gao Yang, Zheng Tao, Qin Geng, Guo Jing, Zeng Tiebo, Han Zhengbin, Zhang Yan, Wu Qiong
School of Life Science and Technology, State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin, 150001, China.
Mol Genet Genomics. 2015 Apr;290(2):685-97. doi: 10.1007/s00438-014-0952-z. Epub 2014 Nov 27.
Long intergenic non-coding RNAs (lincRNAs) as a key group of non-coding RNAs have gained substantial attention. Though lincRNAs have been systematically explored in various mouse tissues and cell lines, large-scale identification of lincRNAs in mouse pre-implantation embryonic development (PED) process has not be documented previously. Therefore, it is important to identify and characterize novel lincRNAs that may be involved in PED. In this paper, we performed transcriptome assembly based on published single-cell RNA-seq data during mouse PED and identified 4,438 putative lincRNAs. Combining these with Ensembl lincRNAs, we established a reference catalog of 5,808 transcribed lincRNAs in PED. We then systematically analyzed the lincRNAs in this reference catalog and revealed that the identified novel PED lincRNAs are generally comparable with known Ensembl lincRNAs in genomic aspects. In addition, the global expression patterns can be separated by zygote first cleavage division in clustering analysis and we further identified and analyzed differentially expressed lincRNAs involved in this process. The expression of lincRNAs involved in the process is negatively correlated with promoter methylation in trend. The identified lincRNAs involved in zygote first cleavage division could have important roles in mouse early embryonic development and need further functional studies. Altogether, a novel reference catalog of mouse PED lincRNAs is provided and characterized, which would be a valuable resource for further functional analyses and may help elucidate the pre-implantation regulatory mechanism.
长链基因间非编码RNA(lincRNAs)作为非编码RNA的一个关键类别,已受到广泛关注。尽管lincRNAs已在各种小鼠组织和细胞系中得到系统研究,但此前尚未有关于在小鼠植入前胚胎发育(PED)过程中大规模鉴定lincRNAs的报道。因此,鉴定和表征可能参与PED的新型lincRNAs具有重要意义。在本文中,我们基于已发表的小鼠PED单细胞RNA测序数据进行转录组组装,鉴定出4438个假定的lincRNAs。将这些与Ensembl lincRNAs相结合,我们建立了一个包含5808个PED中已转录lincRNAs的参考目录。然后,我们对该参考目录中的lincRNAs进行了系统分析,发现鉴定出的新型PED lincRNAs在基因组方面通常与已知的Ensembl lincRNAs相当。此外,在聚类分析中,整体表达模式可通过合子第一次卵裂划分开,我们进一步鉴定并分析了参与此过程的差异表达lincRNAs。参与该过程的lincRNAs的表达在趋势上与启动子甲基化呈负相关。鉴定出的参与合子第一次卵裂的lincRNAs可能在小鼠早期胚胎发育中发挥重要作用,需要进一步进行功能研究。总之,我们提供并表征了一个新型的小鼠PED lincRNAs参考目录,这将是进一步功能分析的宝贵资源,可能有助于阐明植入前的调控机制。