Division of Developmental Biology, The Roslin Institute and R(D)SVS, The University of Edinburgh, Easter Bush, Roslin, Midlothian EH25 9RG, UK.
Reproduction. 2012 Aug;144(2):221-33. doi: 10.1530/REP-12-0025. Epub 2012 May 31.
Little is known about the involvement of microRNAs (miRNAs) in the follicular-luteal transition. The aim of this study was to identify genome-wide changes in miRNAs associated with follicular differentiation in sheep. miRNA libraries were produced from samples collected at defined stages of the ovine oestrous cycle and representing healthy growing follicles, (diameter, 4.0-5.5 mm), pre-ovulatory follicles (6.0-7.0 mm), early corpora lutea (day 3 post-oestrus) and late corpora lutea (day 9). A total of 189 miRNAs reported in sheep or other species and an additional 23 novel miRNAs were identified by sequencing these libraries. miR-21, miR-125b, let-7a and let-7b were the most abundant miRNAs overall, accounting for 40% of all miRNAs sequenced. Examination of changes in cloning frequencies across development identified nine different miRNAs whose expression decreased in association with the follicular-luteal transition and eight miRNAs whose expression increased during this transition. Expression profiles were confirmed by northern analyses, and experimentally validated targets were identified using miRTarBase. A majority of the 29 targets identified represented genes known to be actively involved in regulating follicular differentiation in vivo. Finally, luteinisation of follicular cells in vitro resulted in changes in miRNA levels that were consistent with those identified in vivo, and these changes were temporally associated with changes in the levels of putative miRNA targets in granulosa cells. In conclusion, this is the first study to characterise genome-wide miRNA profiles during different stages of follicle and luteal development. Our data identify a subset of miRNAs that are potentially important regulators of the follicular-luteal transition.
关于 microRNAs(miRNAs)在卵泡黄体转化中的作用知之甚少。本研究旨在鉴定与绵羊卵泡分化相关的miRNAs 的全基因组变化。从绵羊发情周期特定阶段采集的样本中产生了 miRNA 文库,这些样本代表了健康生长的卵泡(直径 4.0-5.5mm)、排卵前卵泡(6.0-7.0mm)、早期黄体(发情后第 3 天)和晚期黄体(发情后第 9 天)。通过测序这些文库,共鉴定出 189 种在绵羊或其他物种中报道的 miRNAs 和 23 种新的 miRNAs。miR-21、miR-125b、let-7a 和 let-7b 是所有测序 miRNA 中最丰富的 miRNA,占所有 miRNA 的 40%。对整个发育过程中克隆频率变化的研究表明,有 9 种不同的 miRNA 表达随卵泡黄体转化而降低,有 8 种 miRNA 表达在转化过程中增加。Northern 分析证实了表达谱,利用 miRTarBase 鉴定了实验验证的靶标。所鉴定的 29 个靶标中的大多数代表了已知在体内积极参与调节卵泡分化的基因。最后,体外卵泡细胞的黄体化导致 miRNA 水平发生变化,这些变化与体内鉴定的变化一致,并且这些变化与颗粒细胞中假定 miRNA 靶标的水平变化在时间上相关。总之,这是首次描述卵泡和黄体发育不同阶段全基因组 miRNA 谱的研究。我们的数据确定了一组潜在的重要卵泡黄体转化调节因子的 miRNAs。