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遗传性隐睾大鼠品系中肌肉和细胞骨架相关基因的表达改变

Altered expression of muscle- and cytoskeleton-related genes in a rat strain with inherited cryptorchidism.

作者信息

Barthold Julia S, McCahan Suzanne M, Singh Amar V, Knudsen Thomas B, Si Xiaoli, Campion Liam, Akins Robert E

机构信息

Nemours Biomedical Research and Division of Urology, A.I. duPont Hospital for Children, Wilmington, Delaware 19803, USA.

出版信息

J Androl. 2008 May-Jun;29(3):352-66. doi: 10.2164/jandrol.107.003970. Epub 2008 Jan 24.

Abstract

Development of the fetal gubernaculum is a prerequisite for testicular descent and dependent on insulin-like 3 and androgen, but knowledge of downstream effectors is limited. We analyzed transcript profiles in gubernaculum and testis to address changes occurring during normal and abnormal testicular descent in Long Evans wild-type (wt) and cryptorchid (orl) fetuses. Total RNA from male wt and orl gubernacula (gestational days [GD]18-20), wt female gubernacula (GD18), and testis (GD17 and 19) was hybridized to Affymetrix GeneChips. Statistical analysis of temporal, gender, and strain-specific differences in gene expression was performed with the use of linear models analysis with empirical Bayes statistics and analysis of variance (gubernaculum) and linear analysis (testis). Overrepresented common gene ontology functional categories and pathways were identified in groups of differentially expressed genes with the Database for Annotation, Visualization, and Integrated Discovery. Transcript profiles were dynamic in wt males between GD18-19 and GD20, comparatively static in orl GD18-20 gubernaculum, and similar in wt and orl testis. Functional analysis of differentially expressed genes in wt and orl gubernaculum identified categories related to metabolism, cellular biogenesis, small GTPase-mediated signal transduction, cytoskeleton, muscle development, and insulin signaling. Genes involved in androgen receptor signaling, regulated by androgens, or both were overrepresented in differentially expressed gubernaculum and testis gene groups. Quantitative reverse transcription polymerase chain reaction (RT-PCR) confirmed differential expression of genes related to muscle development, including Myog, Tnnt2, Fst, Igf1, Igfbp5, Id2, and Msx1. These data suggest that the orl mutation results in a primary gubernacular defect that affects muscle development and cytoskeletal function and might alter androgen-regulated pathways.

摘要

胎儿引带的发育是睾丸下降的前提条件,且依赖于胰岛素样 3 和雄激素,但对下游效应器的了解有限。我们分析了引带和睾丸中的转录谱,以探讨 Long Evans 野生型(wt)和隐睾(orl)胎儿在正常和异常睾丸下降过程中发生的变化。从雄性 wt 和 orl 引带(妊娠天数[GD]18 - 20)、wt 雌性引带(GD18)以及睾丸(GD17 和 19)中提取的总 RNA 与 Affymetrix 基因芯片进行杂交。使用带有经验贝叶斯统计的线性模型分析以及方差分析(引带)和线性分析(睾丸)对基因表达的时间、性别和品系特异性差异进行统计分析。利用注释、可视化和综合发现数据库(Database for Annotation, Visualization, and Integrated Discovery)在差异表达基因组中鉴定出过度富集的常见基因本体功能类别和途径。转录谱在 wt 雄性 GD18 - 19 和 GD20 之间是动态的,在 orl GD18 - 20 引带中相对静态,并且在 wt 和 orl 睾丸中相似。对 wt 和 orl 引带中差异表达基因的功能分析确定了与代谢、细胞生物发生、小 GTP 酶介导的信号转导、细胞骨架、肌肉发育和胰岛素信号传导相关的类别。参与雄激素受体信号传导、受雄激素调节或两者皆有的基因在差异表达的引带和睾丸基因组中过度富集。定量逆转录聚合酶链反应(RT-PCR)证实了与肌肉发育相关的基因存在差异表达,包括 Myog、Tnnt2、Fst、Igf1、Igfbp5、Id2 和 Msx1。这些数据表明,orl 突变导致原发性引带缺陷,影响肌肉发育和细胞骨架功能,并可能改变雄激素调节的途径。

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