胶原修饰Leprecan蛋白在小鼠性腺组织和成熟精子中的表达、表征及功能意义。

AIMS Genetics Pub Date : 2018-01-01 Epub Date: 2018-02-07 DOI:10.3934/genet.2018.1.24
Sarah M Zimmerman, Roberta Besio, Melissa E Heard-Lipsmeyer, Milena Dimori, Patrizio Castagnola, Frances L Swain, Dana Gaddy, Alan B Diekman, Roy Morello
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引用次数: 5

摘要

Leprecan蛋白家族包括脯氨酸3-羟化酶(P3H1, P3H2和P3H3),密切相关的软骨相关蛋白(CRTAP)和SC65 (Synaptonemal complex 65,又名P3H4, LEPREL4),参与原纤维胶原的翻译后修饰。CRTAP、P3H1和P3H2突变导致人类遗传疾病。我们最近表明,SC65在内质网中与P3H3和赖基羟化酶1形成稳定的复合物,该复合物的缺失导致胶原赖基羟化缺陷,导致骨量降低和皮肤脆弱。有趣的是,SC65最初被描述为一种突触复合物相关蛋白,这表明它在种系细胞中有潜在的额外作用。在本研究中,我们描述了SC65, CRTAP和其他Leprecan蛋白在出生后小鼠生殖器官中的表达。我们检测到SC65在4周龄以内的睾丸小管周围细胞中表达,但在精管细胞中不表达,而其在卵泡中表达直到成年。与骨和皮肤类似,SC65和P3H3在睾丸和卵巢中也紧密共表达。此外,我们发现CRTAP,一种通常参与胶原脯氨酸3-羟基化的蛋白,在卵巢的卵泡和基质以及4周龄的睾丸间质细胞、种系细胞和成熟精子中高度表达。重要的是,CrtapKO小鼠在形态异常的成熟精子中有轻微但显著的增加(与WT相比增加了17%)。这些数据表明Leprecans在生殖器官基质中表达的胶原翻译后修饰中的作用。虽然我们无法证实SC65是突触复合体的一部分,但CRTAP在精管和成熟精子中的表达表明,它在睾丸生殖细胞谱系和精子形态发生中发挥了作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Expression characterization and functional implication of the collagen-modifying Leprecan proteins in mouse gonadal tissue and mature sperm.

Expression characterization and functional implication of the collagen-modifying Leprecan proteins in mouse gonadal tissue and mature sperm.

Expression characterization and functional implication of the collagen-modifying Leprecan proteins in mouse gonadal tissue and mature sperm.

Expression characterization and functional implication of the collagen-modifying Leprecan proteins in mouse gonadal tissue and mature sperm.

The Leprecan protein family which includes the prolyl 3-hydroxylase enzymes (P3H1, P3H2, and P3H3), the closely related cartilage-associated protein (CRTAP), and SC65 (Synaptonemal complex 65, aka P3H4, LEPREL4), is involved in the post-translational modification of fibrillar collagens. Mutations in CRTAP, P3H1 and P3H2 cause human genetic diseases. We recently showed that SC65 forms a stable complex in the endoplasmic reticulum with P3H3 and lysyl hydroxylase 1 and that loss of this complex leads to defective collagen lysyl hydroxylation and causes low bone mass and skin fragility. Interestingly, SC65 was initially described as a synaptonemal complex-associated protein, suggesting a potential additional role in germline cells. In the present study, we describe the expression of SC65, CRTAP and other Leprecan proteins in postnatal mouse reproductive organs. We detect SC65 expression in peritubular cells of testis up to 4 weeks of age but not in cells within seminiferous tubules, while its expression is maintained in ovarian follicles until adulthood. Similar to bone and skin, SC65 and P3H3 are also tightly co-expressed in testis and ovary. Moreover, we show that CRTAP, a protein normally involved in collagen prolyl 3-hydroxylation, is highly expressed in follicles and stroma of the ovary and in testes interstitial cells at 4 weeks of age, germline cells and mature sperm. Importantly, CrtapKO mice have a mild but significant increase in morphologically abnormal mature sperm (17% increase compared to WT). These data suggest a role for the Leprecans in the post-translational modification of collagens expressed in the stroma of the reproductive organs. While we could not confirm that SC65 is part of the synaptonemal complex, the expression of CRTAP in the seminiferous tubules and in mature sperm suggest a role in the testis germ cell lineage and sperm morphogenesis.

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AIMS Genetics
AIMS Genetics GENETICS & HEREDITY-
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