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本文引用的文献

1
Epididymal protein Rnase10 is required for post-testicular sperm maturation and male fertility.附睾蛋白 Rnase10 对于睾丸后精子成熟和雄性生育力是必需的。
FASEB J. 2012 Oct;26(10):4198-209. doi: 10.1096/fj.12-205211. Epub 2012 Jun 29.
2
Classification of mouse sperm motility patterns using an automated multiclass support vector machines model.使用自动化多类支持向量机模型对小鼠精子运动模式进行分类。
Biol Reprod. 2011 Jun;84(6):1207-15. doi: 10.1095/biolreprod.110.088989. Epub 2011 Feb 23.
3
Inhibition of Ser/Thr phosphatases induces capacitation-associated signaling in the presence of Src kinase inhibitors.在 Src 激酶抑制剂存在的情况下,抑制丝氨酸/苏氨酸磷酸酶可诱导顶体反应相关信号转导。
J Biol Chem. 2010 Mar 12;285(11):7977-85. doi: 10.1074/jbc.M109.085845. Epub 2010 Jan 12.
4
Human ribonuclease 9, a member of ribonuclease A superfamily, specifically expressed in epididymis, is a novel sperm-binding protein.人核糖核酸酶9是核糖核酸酶A超家族的成员,在附睾中特异性表达,是一种新型的精子结合蛋白。
Asian J Androl. 2009 Mar;11(2):240-51. doi: 10.1038/aja.2008.30. Epub 2009 Jan 12.
5
New insights into epididymal biology and function.附睾生物学与功能的新见解。
Hum Reprod Update. 2009 Mar-Apr;15(2):213-27. doi: 10.1093/humupd/dmn055. Epub 2009 Jan 8.
6
Tyrosylprotein sulfotransferase-2 expression is required for sulfation of RNase 9 and Mfge8 in vivo.体内核糖核酸酶9(RNase 9)和乳脂肪球表皮生长因子8(Mfge8)的硫酸化需要酪氨酰蛋白硫酸转移酶-2的表达。
J Biol Chem. 2009 Jan 30;284(5):3096-3105. doi: 10.1074/jbc.M808434200. Epub 2008 Dec 1.
7
Cloning, expression and location of RNase9 in human epididymis.核糖核酸酶9在人附睾中的克隆、表达及定位
BMC Res Notes. 2008 Nov 10;1:111. doi: 10.1186/1756-0500-1-111.
8
Proteomic changes in mammalian spermatozoa during epididymal maturation.附睾成熟过程中哺乳动物精子的蛋白质组变化
Asian J Androl. 2007 Jul;9(4):554-64. doi: 10.1111/j.1745-7262.2007.00280.x.
9
The rat epididymal transcriptome: comparison of segmental gene expression in the rat and mouse epididymides.大鼠附睾转录组:大鼠和小鼠附睾节段性基因表达的比较。
Biol Reprod. 2007 Apr;76(4):561-70. doi: 10.1095/biolreprod.106.057323. Epub 2006 Dec 13.
10
Detection and purification of tyrosine-sulfated proteins using a novel anti-sulfotyrosine monoclonal antibody.使用新型抗硫酸化酪氨酸单克隆抗体检测和纯化硫酸化酪氨酸蛋白
J Biol Chem. 2006 Dec 8;281(49):37877-87. doi: 10.1074/jbc.M609398200. Epub 2006 Oct 17.

RNASE9基因敲除小鼠精子成熟受损。

Impaired sperm maturation in RNASE9 knockout mice.

作者信息

Westmuckett Andrew D, Nguyen Edward B, Herlea-Pana Oana M, Alvau Antonio, Salicioni Ana M, Moore Kevin L

机构信息

Cardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma.

Department of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.

出版信息

Biol Reprod. 2014 Jun;90(6):120. doi: 10.1095/biolreprod.113.116863. Epub 2014 Apr 9.

DOI:10.1095/biolreprod.113.116863
PMID:24719258
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4093998/
Abstract

Ribonuclease, RNase A family, 9 (RNASE9) is a ribonuclease A superfamily member that is expressed only in the epididymis. It is a small, secreted polypeptide, it lacks ribonuclease activity, and its function(s) is unknown. However, epididymis-specific expression suggests a role in sperm maturation. We generated Rnase9(-/-) mice to study RNASE9 function in vivo. We confirm that RNASE9 expression is restricted to the epididymis. Within the epididymis, RNASE9 is first detected in midcaput, persists through the distal caput and corpus, and wanes in the cauda. Rnase9(-/-) mice are born at the expected Mendelian ratio, have normal postnatal growth and development, and have no outwardly apparent phenotype. Spermatogenesis is normal, and Rnase9-null sperm are morphologically normal. Rnase9(-/-) males have normal fertility in unrestricted mating trials, and fertilization rates in in vitro fertilization assays are indistinguishable from wild-type mice. Visual observations coupled with analyses of sperm velocities shortly after swim out from the corpus shows that motility of Rnase9-null sperm is significantly impaired. However, no differences between wild-type and Rnase9-null sperm are detected by computer-assisted sperm analysis 10-90 min after sperm isolation from the corpus or cauda. Assessment of capacitation-dependent signaling pathways in Rnase9-null sperm showed that, while levels of tyrosine phosphorylation of sperm proteins were normal, there was decreased phosphorylation of protein kinase A substrates upon capacitation compared to wild-type mice. In conclusion, RNASE9 is dispensable for fertility, but the absence of RNASE9 during epididymal transit results in impaired sperm maturation.

摘要

核糖核酸酶,RNase A家族,9(RNASE9)是核糖核酸酶A超家族成员,仅在附睾中表达。它是一种小的分泌型多肽,缺乏核糖核酸酶活性,其功能尚不清楚。然而,附睾特异性表达表明其在精子成熟中起作用。我们生成了Rnase9(-/-)小鼠以研究RNASE9在体内的功能。我们证实RNASE9的表达仅限于附睾。在附睾内,RNASE9首先在附睾头中部被检测到,在附睾头远端和体部持续存在,并在附睾尾减弱。Rnase9(-/-)小鼠以预期的孟德尔比例出生,出生后生长发育正常,没有明显的外在表型。精子发生正常,Rnase9基因缺失的精子形态正常。在无限制交配试验中,Rnase9(-/-)雄性具有正常的生育能力,体外受精试验中的受精率与野生型小鼠无差异。从附睾体部游出后不久,通过视觉观察和精子速度分析表明,Rnase9基因缺失的精子活力明显受损。然而,在从附睾体部或尾部分离精子10 - 90分钟后,通过计算机辅助精子分析未检测到野生型和Rnase9基因缺失的精子之间存在差异。对Rnase9基因缺失的精子中获能依赖性信号通路的评估表明,虽然精子蛋白的酪氨酸磷酸化水平正常,但与野生型小鼠相比,获能时蛋白激酶A底物的磷酸化减少。总之,RNASE9对生育能力并非必需,但在附睾转运过程中缺乏RNASE9会导致精子成熟受损。