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首页> 外文期刊>Biology of Reproduction: Offical Journal of the Society for the Study of Reproduction >The rat epididymal transcriptome: Comparison of segmental gene expression in the rat and mouse epididymides
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The rat epididymal transcriptome: Comparison of segmental gene expression in the rat and mouse epididymides

机译:大鼠附睾转录组:大鼠和小鼠附睾中节段基因表达的比较

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Regional differences along the epididymis are essential for the establishment of the luminal environment required for sperm maturation. In the current study, 19 morphologically distinct segments of the rat epididymis were identified by microdissection. Total RNA was isolated from each segment and subjected to microarray analysis. Segmental analysis of epididymal gene expression identified more than 16000 expressed qualifiers, whereas profiling of RNA from whole rat epididymis identified approximately 12 000 expressed qualifiers. Screening a panel of normal rat tissues identified both epididymal-selective and epididymal-specific transcripts. In addition, more than 3500 qualifiers were shown to be present and differentially upregulated or downregulated by more than fourfold between any two segments. The present study complements our previous segment-dependent analysis of gene expression in the mouse epididymis and allows for comparative analyses between datasets. A total of 492 genes was shown to be present on both the MOE430 (mouse) and RAE230_2 (rat) microarrays, expressed in the epididymis of both species, and differentially expressed by more than fourfold in between segments in each species. Moreover, in-depth quantitative RT-PCR analysis of 36 members of the beta defensin gene family showed highly conserved patterns of expression along the lengths of the mouse and rat epididymides. These analyses elucidate global gene expression patterns along the length of the rat epididymis and provide a novel evaluation of conserved and nonconserved gene expression patterns in the epididymides of the two species. Furthermore, these data provide a powerful resource for the research community for future studies of biological factors that mediate sperm maturation and storage.
机译:沿附睾的区域差异对于建立精子成熟所需的腔环境至关重要。在当前的研究中,通过显微解剖鉴定了大鼠附睾的19个形态学上不同的部分。从每个片段中分离总RNA,并进行微阵列分析。附睾基因表达的分段分析确定了超过16000个表达的限定词,而从整个大鼠附睾中提取的RNA谱图鉴定了大约12000个表达的限定词。筛选一组正常大鼠组织可识别附睾选择性和附睾特异性转录本。此外,显示存在3500多个预选赛,并且在任何两个段之间的差异上调或下调的幅度均超过四倍。本研究补充了我们先前对小鼠附睾中基因表达的片段依赖性分析,并允许在数据集之间进行比较分析。共有492个基因显示在MOE430(小鼠)和RAE230_2(大鼠)微阵列上,在两个物种的附睾中表达,并且在每个物种的片段之间差异表达超过四倍。此外,对β防御素基因家族的36个成员的深入定量RT-PCR分析显示,沿小鼠和大鼠附睾长度的高度保守的表达模式。这些分析阐明了沿大鼠附睾长度的总体基因表达模式,并提供了对两种物种的附睾中保守和非保守基因表达模式的新颖评估。此外,这些数据为研究界提供了有力的资源,可用于将来对介导精子成熟和贮藏的生物学因素的研究。

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