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2
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Mice expressing aberrant sperm-specific protein PMIS2 produce normal-looking but fertilization-incompetent spermatozoa.表达异常精子特异性蛋白 PMIS2 的小鼠产生外观正常但受精能力丧失的精子。
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本文引用的文献

1
Fertilization: a sperm's journey to and interaction with the oocyte.受精:精子的旅程及其与卵子的相互作用。
J Clin Invest. 2010 Apr;120(4):984-94. doi: 10.1172/JCI41585. Epub 2010 Apr 1.
2
N-glycan structures: recognition and processing in the ER.N-糖链结构:内质网中的识别与加工。
Trends Biochem Sci. 2010 Feb;35(2):74-82. doi: 10.1016/j.tibs.2009.10.001. Epub 2009 Oct 21.
3
Specific ER quality control components required for biogenesis of the plant innate immune receptor EFR.植物先天免疫受体EFR生物合成所需的特定内质网质量控制组件。
Proc Natl Acad Sci U S A. 2009 Sep 15;106(37):15973-8. doi: 10.1073/pnas.0905532106. Epub 2009 Aug 26.
4
Protein folding, misfolding and disease.蛋白质折叠、错误折叠与疾病。
FEBS Lett. 2009 Aug 20;583(16):2579-80. doi: 10.1016/j.febslet.2009.07.016. Epub 2009 Jul 16.
5
Disruption of ADAM3 impairs the migration of sperm into oviduct in mouse.ADAM3的破坏会损害小鼠精子向输卵管的迁移。
Biol Reprod. 2009 Jul;81(1):142-6. doi: 10.1095/biolreprod.108.074021. Epub 2009 Apr 1.
6
The ubiquitylation machinery of the endoplasmic reticulum.内质网的泛素化机制
Nature. 2009 Mar 26;458(7237):453-60. doi: 10.1038/nature07962.
7
Calreticulin, a multi-process calcium-buffering chaperone of the endoplasmic reticulum.钙网蛋白,一种内质网的多功能钙缓冲伴侣蛋白。
Biochem J. 2009 Feb 1;417(3):651-66. doi: 10.1042/BJ20081847.
8
Sperm-egg fusion assay in mammals.哺乳动物的精卵融合试验。
Methods Mol Biol. 2008;475:335-45. doi: 10.1007/978-1-59745-250-2_19.
9
Lectin-deficient calreticulin retains full functionality as a chaperone for class I histocompatibility molecules.凝集素缺陷型钙网蛋白作为I类组织相容性分子的伴侣分子保留了完整的功能。
Mol Biol Cell. 2008 Jun;19(6):2413-23. doi: 10.1091/mbc.e07-10-1055. Epub 2008 Mar 12.
10
N-glycan structure dictates extension of protein folding or onset of disposal.N-聚糖结构决定蛋白质折叠的延伸或降解的开始。
Nat Chem Biol. 2007 Jun;3(6):313-20. doi: 10.1038/nchembio880.

钙网蛋白是一种睾丸特异性伴侣蛋白,对于精子的生育能力是必需的。

Calsperin is a testis-specific chaperone required for sperm fertility.

机构信息

Research Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871, Japan.

出版信息

J Biol Chem. 2011 Feb 18;286(7):5639-46. doi: 10.1074/jbc.M110.140152. Epub 2010 Dec 3.

DOI:10.1074/jbc.M110.140152
PMID:21131354
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3037677/
Abstract

Calnexin (CANX) and calreticulin (CALR) are homologous lectin chaperones located in the endoplasmic reticulum and cooperate to mediate nascent glycoprotein folding. In the testis, calmegin (CLGN) and calsperin (CALR3) are expressed as germ cell-specific counterparts of CANX and CALR, respectively. Here, we show that Calr3(-/-) males produced apparently normal sperm but were infertile because of defective sperm migration from the uterus into the oviduct and defective binding to the zona pellucida. Whereas CLGN was required for ADAM1A/ADAM2 dimerization and subsequent maturation of ADAM3, a sperm membrane protein required for fertilization, we show that CALR3 is a lectin-deficient chaperone directly required for ADAM3 maturation. Our results establish the client specificity of CALR3 and demonstrate that the germ cell-specific CALR-like endoplasmic reticulum chaperones have contrasting functions in the development of male fertility. The identification and understanding of the maturation mechanisms of key sperm proteins will pave the way toward novel approaches for both contraception and treatment of unexplained male infertility.

摘要

钙连蛋白 (CANX) 和钙网蛋白 (CALR) 是位于内质网中的同源凝集素伴侣,协同介导新生糖蛋白折叠。在睾丸中,calmegin (CLGN) 和 calsperin (CALR3) 分别作为 CANX 和 CALR 的生殖细胞特异性对应物表达。在这里,我们表明 Calr3(-/-) 雄性产生的精子明显正常,但由于精子从子宫迁移到输卵管和与透明带结合的缺陷而不育。虽然 CLGN 是 ADAM1A/ADAM2 二聚体化和随后成熟所需的精子膜蛋白 ADAM3 所必需的,但我们表明 CALR3 是一种缺乏凝集素的伴侣,直接参与 ADAM3 的成熟。我们的结果确定了 CALR3 的客户特异性,并证明了生殖细胞特异性的类似 CALR 的内质网伴侣在男性生育力发育中具有相反的功能。关键精子蛋白成熟机制的鉴定和理解将为避孕和治疗不明原因男性不育症开辟新途径。