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Members of the CDY family have different expression patterns: CDY1 transcripts have the best correlation with complete spermatogenesis.

作者信息

Kleiman Sandra E, Yogev Leah, Hauser Ron, Botchan Amnon, Bar-Shira Maymon Batia, Schreiber Letizia, Paz Gedalia, Yavetz Haim

机构信息

Institute for the Study of Fertility, Lis Maternity Hospital, Tel Aviv Sourasky Medical Center, Sackler Faculty of Medicine, Tel Aviv University, 6 Weizman Street, 64239 Tel Aviv, Israel.

出版信息

Hum Genet. 2003 Nov;113(6):486-92. doi: 10.1007/s00439-003-0990-9. Epub 2003 Sep 3.

DOI:10.1007/s00439-003-0990-9
PMID:14569460
Abstract

The CDY family of genes is of special interest because some of them are included in chromosome-Y microdeletions detected among infertile men and are apparently involved in the spermiogenetic process. In this study, we employed the reverse transcriptase/polymerase chain reaction technique to test the RNA expression of the various transcripts of these genes in testicular biopsies of 84 azoospermic men who had been classified by comprehensive histology and cytology analyses. We also evaluated the feasibility of detecting CDY expression in biopsies taken by testicular sperm extraction versus acquisition by aspiration. There was a significant association between the type of testicular impairment and the expression of CDY1 and CDY2 transcripts. CDY2 was expressed whenever germ cells were present, but CDY1 major and especially CDY1 minor and short transcripts were identified almost exclusively when mature spermatids/spermatozoa were detected. The expression of CDY1 minor and short transcripts detected in aspirated specimens was less efficient than that in testicular tissue acquired by extraction. It is suggested that CDY2 is apparently required in the early stages of spermatogenesis, whereas CDY1 transcripts are required later on in the process. The findings of this study imply different functional roles for CDY isoforms during spermatogenesis. However, in consideration of the high levels of identity between CDY1 and CDY2 (98% at the protein level), the delayed up-regulation of CDY1 transcripts could be attributable to temporal changes in dosage requirements.

摘要

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Clinical characterization of 42 oligospermic or azoospermic men with microdeletion of the AZFc region of the Y chromosome, and of 18 children conceived via ICSI.42例Y染色体AZFc区域微缺失的少精子症或无精子症男性以及18例通过卵胞浆内单精子注射(ICSI)受孕儿童的临床特征
Hum Reprod. 2002 Nov;17(11):2813-24. doi: 10.1093/humrep/17.11.2813.
2
Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure.人类Y染色体上回文序列P5和P1之间的重组会导致大量缺失和生精障碍。
Am J Hum Genet. 2002 Oct;71(4):906-22. doi: 10.1086/342928. Epub 2002 Sep 20.
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Cyclin A1 and gametogenesis in fertile and infertile patients: a potential new molecular diagnostic marker.
CDYL2 转录本变体在乳腺癌生长和转移中的离散功能和机制作用。
Theranostics. 2020 Apr 6;10(12):5242-5258. doi: 10.7150/thno.43744. eCollection 2020.
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Germline deletion of Cdyl causes teratozoospermia and progressive infertility in male mice.胚系缺失 Cdyl 导致雄性小鼠的畸形精子症和进行性不育。
Cell Death Dis. 2019 Mar 8;10(3):229. doi: 10.1038/s41419-019-1455-y.
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Azoospermia factor and male infertility.无精子症因子与男性不育
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Expression level of chromodomain Y (CDY): potential marker for prediction of sperm recovery in non-obstructive azoospermia.Y染色体染色体结构域(CDY)的表达水平:非梗阻性无精子症患者精子恢复预测的潜在标志物
Int J Reprod Biomed. 2016 Jun;14(6):383-8.
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Distinctive pattern of expression of spermatogenic molecular markers in testes of azoospermic men with non-mosaic Klinefelter syndrome.非嵌合型克兰费尔特综合征无精子症男性睾丸中生精分子标志物的独特表达模式。
J Assist Reprod Genet. 2016 Jun;33(6):807-14. doi: 10.1007/s10815-016-0698-0. Epub 2016 Mar 19.
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Copy-number variations in Y-chromosomal azoospermia factor regions identified by multiplex ligation-dependent probe amplification.通过多重连接依赖探针扩增鉴定的Y染色体无精子症因子区域的拷贝数变异。
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9
Organizational and functional status of the Y-linked genes and loci in the infertile patients having normal spermiogram.不育患者中 Y 连锁基因和位点的组织和功能状态,其精液常规检查正常。
PLoS One. 2012;7(7):e41488. doi: 10.1371/journal.pone.0041488. Epub 2012 Jul 23.
10
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Identification and characterization of the cynomolgus monkey chromodomain gene cynCDY, an orthologue of the human CDY gene family.食蟹猴染色体结构域基因cynCDY的鉴定与特征分析,该基因是人类CDY基因家族的一个直系同源基因。
Mol Hum Reprod. 2002 Aug;8(8):702-9. doi: 10.1093/molehr/8.8.702.
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Previously uncharacterized histone acetyltransferases implicated in mammalian spermatogenesis.先前未被鉴定的与哺乳动物精子发生有关的组蛋白乙酰转移酶。
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The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men.Y染色体的AZFc区域具有大量回文序列,且在不育男性中存在一致的复发性缺失。
Nat Genet. 2001 Nov;29(3):279-86. doi: 10.1038/ng757.
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A possible meiotic function of the peculiar patterns of gene expression in mammalian spermatogenic cells.哺乳动物生精细胞中基因表达独特模式的一种可能的减数分裂功能。
Mech Dev. 2001 Aug;106(1-2):3-23. doi: 10.1016/s0925-4773(01)00413-0.
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Expression of CDY1 may identify complete spermatogenesis.CDY1的表达可能有助于识别完全精子发生。
Fertil Steril. 2001 Jan;75(1):166-73. doi: 10.1016/s0015-0282(00)01639-3.
10
Regulated hyperacetylation of core histones during mouse spermatogenesis: involvement of histone deacetylases.小鼠精子发生过程中核心组蛋白的调控性超乙酰化:组蛋白去乙酰化酶的作用
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