首页> 美国卫生研究院文献>Data in Brief >Transcriptome datasets of ESR2-regulated genes in rat granulosa cells during gonadotropin-induced follicle maturation
【2h】

Transcriptome datasets of ESR2-regulated genes in rat granulosa cells during gonadotropin-induced follicle maturation

机译:促性腺激素诱导的卵泡成熟过程中大鼠颗粒细胞中ESR2调控基因的转录组数据集

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

Disruption of estrogen receptor beta (ESR2) dysregulates granulosa cell genes essential for follicle maturation and ovulation. The datasets presented in this article depict gonadotropin-induced genes, which are differentially expressed in -null rat granulosa cells. Synchronized follicle development was initiated in four-week-old wildtype and -null female rats by administration of PMSG. Forty-eight hours after PMSG injection, further maturation of ovarian follicles was induced by hCG treatment. Granulosa cells were collected from the ovaries before gonadotropin administration, 48 h after PMSG treatment, and 4 h after hCG injection to the PMSG-treated rats. Total RNA was purified from granulosa cells and whole transcriptome was assessed by RNA-sequencing on an Illumina HiSeq X platform. RNA-seq data of wildtype and -null granulosa cells were analyzed and differentially expressed genes were identified by CLC Genomics Workbench. Gonadotropin-induced genes were identified by comparing the transcriptome data of PMSG- or hCG-induced wildtype granulosa cells with those without gonadotropin treatment. Furthermore, differentially expressed genes in -null granulosa cells were determined by comparing the transcriptome data with that of wildtype granulosa cells. These datasets can be used to recognize the gonadotropin-induced genes in granulosa cells that are -regulated and important for ovarian follicle maturation.
机译:破坏雌激素受体β(ESR2)失调了卵泡成熟和排卵所必需的颗粒细胞基因。本文提供的数据集描述了促性腺激素诱导的基因,这些基因在空的大鼠颗粒细胞中差异表达。通过给予PMSG,在四周大的野生型和零雌性雌性大鼠中开始同步卵泡发育。注射PMSG后48小时,通过hCG处理诱导卵巢卵泡进一步成熟。给予促性腺激素前,PMSG治疗后48 h和hCG注射PMSG处理的大鼠后4 h,从卵巢收集颗粒细胞。从颗粒细胞纯化总RNA,并在Illumina HiSeq X平台上通过RNA测序评估整个转录组。分析野生型和空颗粒细胞的RNA-seq数据,并通过CLC基因组学工作台鉴定差异表达的基因。通过比较PMSG或hCG诱导的野生型颗粒细胞与未经促性腺激素处理的细胞的转录组数据,鉴定促性腺激素诱导的基因。此外,通过比较转录组数据与野生型颗粒细胞的转录组数据,确定了无颗粒细胞中差异表达的基因。这些数据集可用于识别粒细胞中促性腺激素诱导的基因,这些基因对卵巢卵泡成熟至关重要。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号