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本文引用的文献

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Methylation status of imprinted genes and repetitive elements in sperm DNA from infertile males.不育男性精子 DNA 中印迹基因和重复元件的甲基化状态。
Sex Dev. 2011;5(2):60-9. doi: 10.1159/000323806. Epub 2011 Feb 4.
2
Imprinting disorders and assisted reproductive technology.印迹缺陷与辅助生殖技术。
Curr Opin Endocrinol Diabetes Obes. 2010 Dec;17(6):517-22. doi: 10.1097/MED.0b013e32834040a3.
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A practical approach to testicular biopsy interpretation for male infertility.实用的睾丸活检解读方法在男性不育症中的应用。
Arch Pathol Lab Med. 2010 Aug;134(8):1197-204. doi: 10.5858/2009-0379-RA.1.
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RFX2 is a candidate downstream amplifier of A-MYB regulation in mouse spermatogenesis.RFX2是小鼠精子发生过程中A-MYB调控的下游候选放大因子。
BMC Dev Biol. 2009 Dec 9;9:63. doi: 10.1186/1471-213X-9-63.
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Assisted reproductive technologies do not enhance the variability of DNA methylation imprints in human.辅助生殖技术不会增强人类 DNA 甲基化印迹的可变性。
J Med Genet. 2010 Jun;47(6):371-6. doi: 10.1136/jmg.2009.073189. Epub 2009 Nov 30.
6
Tissue-specific differentially methylated regions of the human VASA gene are potentially associated with maturation arrest phenotype in the testis.人类VASA基因的组织特异性差异甲基化区域可能与睾丸成熟停滞表型相关。
J Hum Genet. 2009 Aug;54(8):450-6. doi: 10.1038/jhg.2009.59. Epub 2009 Jul 24.
7
Methylation defects of imprinted genes in human testicular spermatozoa.人类睾丸精子中印迹基因的甲基化缺陷。
Fertil Steril. 2010 Jul;94(2):585-94. doi: 10.1016/j.fertnstert.2009.02.051. Epub 2009 Apr 1.
8
Tissue specific differentially methylated regions (TDMR): Changes in DNA methylation during development.组织特异性差异甲基化区域(TDMR):发育过程中DNA甲基化的变化。
Genomics. 2009 Feb;93(2):130-9. doi: 10.1016/j.ygeno.2008.09.003. Epub 2008 Nov 13.
9
An integrated resource for genome-wide identification and analysis of human tissue-specific differentially methylated regions (tDMRs).用于全基因组范围内鉴定和分析人类组织特异性差异甲基化区域(tDMRs)的综合资源。
Genome Res. 2008 Sep;18(9):1518-29. doi: 10.1101/gr.077479.108. Epub 2008 Jun 24.
10
A novel CpG island set identifies tissue-specific methylation at developmental gene loci.一组新的CpG岛可识别发育基因位点的组织特异性甲基化。
PLoS Biol. 2008 Jan;6(1):e22. doi: 10.1371/journal.pbio.0060022.

GTF2A1L 启动子 TDMR 的异常甲基化不会通过 TESE 影响低精子发生症患者的受精率。

Aberrant methylation of the TDMR of the GTF2A1L promoter does not affect fertilisation rates via TESE in patients with hypospermatogenesis.

机构信息

Departments of Integrative Cancer Therapy and Urology, Andrology Unit, Kanazawa University Graduate School of Medical Science, Takara, Kanazawa, Japan.

出版信息

Asian J Androl. 2013 Sep;15(5):634-9. doi: 10.1038/aja.2013.56. Epub 2013 Jun 17.

DOI:10.1038/aja.2013.56
PMID:23770943
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3881655/
Abstract

Increasing evidence shows a relationship between epigenetic regulation and male infertility. The GTF2A1L gene promoter contains the DNA methylation site of a tissue-specific differentially methylated region (TDMR). Eighty-six patients with non-obstructive azoospermia were assessed for the DNA methylation state of CpG islands in the GTF2A1L promoter using testicular genomic DNA. Based on histological criteria, 26 of the 86 patients had normal spermatogenesis (controls), 17 had hypospermatogenesis and 26 had a Sertoli cell-only phenotype or tubular sclerosis. GTF2A1L TDMR methylation was significantly lower in testes DNA from control samples than from hypospermatogenic samples (P=0.029). Patients with hypospermatogenesis were divided into two subgroups: high DNA methylation (HM, n=5) and low DNA methylation (LM, n=12). The GTF2A1L TDMR methylation rate differed significantly between the HM and LM groups (P=0.0019), and GTF2A1L expression was significantly higher among the LM than in the HM patients (P=0.023). High TDMR methylation was correlated with low GTF2A1L gene expression levels. Both groups demonstrated relatively good outcomes with respect to sperm retrieval, fertilisation, pregnancy and childbirth rates. We observed that aberrant GTF2A1L gene expression was not correlated with fertilisation rates. The testicular sperm extraction (TESE) technique may be used to overcome male infertility due to aberrant TDMR methylation.

摘要

越来越多的证据表明,表观遗传调控与男性不育之间存在关系。GTF2A1L 基因启动子包含组织特异性差异甲基化区域 (TDMR) 的 DNA 甲基化位点。使用睾丸基因组 DNA 评估 86 例非梗阻性无精子症患者 GTF2A1L 启动子中 CpG 岛的 DNA 甲基化状态。根据组织学标准,86 例患者中有 26 例具有正常生精功能(对照组),17 例为生精功能低下,26 例为 Sertoli 细胞仅表型或小管硬化。与生精功能低下的样本相比,对照组睾丸 DNA 中的 GTF2A1L TDMR 甲基化显著降低(P=0.029)。生精功能低下的患者分为两组:高 DNA 甲基化(HM,n=5)和低 DNA 甲基化(LM,n=12)。HM 和 LM 组之间的 GTF2A1L TDMR 甲基化率差异显著(P=0.0019),LM 组的 GTF2A1L 表达明显高于 HM 组(P=0.023)。高 TDMR 甲基化与 GTF2A1L 基因表达水平降低相关。两组在精子获取、受精、妊娠和分娩率方面均取得了较好的结果。我们观察到,异常的 GTF2A1L 基因表达与受精率无关。睾丸精子提取(TESE)技术可能用于克服因 TDMR 甲基化异常导致的男性不育。