Global transcriptome analysis of peripheral blood identifies the most significantly down‐regulated genes associated with metabolism regulation in Klinefelter syndrome. Issue 1 (7th January 2015)

• Record Type: Journal Article
• Authors: Huang, Jin; Zhang, Liang; Deng, Hua; Chang, Liang; Liu, Qinli; Liu, Ping
• Is Part Of: Molecular reproduction and development. Volume 82:Issue 1(2015:Jan.)
• Page Start: 17
• Page End: 25
• Publication Date: 2015-01-07
• Subjects: Reproduction -- Periodicals; Molecular biology -- Periodicals; Molecular genetics -- Periodicals; Embryology -- Periodicals; 571.8
• DOI: 10.1002/mrd.22438
• Languages: English
• ISSNs: 1040-452X

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>SUMMARY</title> <sec id="mrd22438-sec-0001" sec-type="section"> <p>The molecular pathogenesis of Klinefelter Syndrome (KS) is not fully understood. The aim of this study was to determine differences in gene expression patterns between KS patients and control individuals to help identify disease‐related genes and biological pathways. Gene expression profiles of five KS patients and five healthy men were determined by microarray; 21 differentially expressed genes with a fold‐change &gt;1.5 and q‐value &lt;0.05 were identified between the groups. Genes associated with metabolism regulation and encoding liver fatty acid‐binding protein (FABP1), aldehyde dehydrogenase 1 family member L1 (ALDH1L1), and vitronectin (VTN) were the most‐significantly down‐regulated in KS, as confirmed by quantitative reverse transcription PCR. Notably, none of these differentially expressed genes are normally found on the X chromosome. Thus, our results indicate that aberrant metabolism is involved in the pathogenesis of KS. Further elucidation of the how aberrant expression of metabolism‐related genes affect the pathogenesis of KS may lead to the development of novel preventative and therapeutic strategies. <italic>Mol. Reprod. Dev. 82: 17–25, 2015. © 2014 Wiley Periodicals, Inc</italic>.</p> </sec> </abstract>