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哺乳动物雄性生殖系细胞中的端粒。

Telomeres in mammalian male germline cells.

作者信息

Zalenskaya Irina A, Zalensky Andrei O

机构信息

Department of Biological Chemistry, School of Medicine, University of California, Davis 95616, USA.

出版信息

Int Rev Cytol. 2002;218:37-67. doi: 10.1016/s0074-7696(02)18011-9.

DOI:10.1016/s0074-7696(02)18011-9
PMID:12199519
Abstract

Telomeres are terminal chromosomal domains that protect chromosome ends from degradation and fusion and promote complete replication of DNA. Telomeres are involved in the regulation of cellular replicative lifespan and tumorigenesis. These important functions of the telomeres have evoked high interest: numerous studies have resulted in a detailed description of telomere composition and structure in somatic cells. Much less is known about telomeres in germline cells. Emerging novel features and unique behavior of telomeres in the process of gamete differentiation suggest that they may have additional germline-specific function(s). This review describes recent studies revealing changes in the telomere organization in the course of differentiation from the germline stem cells to mature sperm in mammals. Similarities and differences between somatic and spermatogenic cells in telomere nuclear localization, protein composition, DNA length, telomerase activity, and chromatin structure are discussed. The exceptional features of the germline telomeres may be important for regulation of telomerase activity during spermatogenesis, homologous chromosome pairing during recombination, as well as for male pronucleus development and ordered chromosome withdrawal post-fertilization.

摘要

端粒是染色体末端结构域,可保护染色体末端免于降解和融合,并促进DNA的完全复制。端粒参与细胞复制寿命和肿瘤发生的调控。端粒的这些重要功能引起了人们的高度关注:大量研究详细描述了体细胞中端粒的组成和结构。而对于生殖细胞中的端粒,人们了解得较少。端粒在配子分化过程中出现的新特征和独特行为表明,它们可能具有额外的生殖细胞特异性功能。本综述描述了最近的研究,揭示了哺乳动物从生殖系干细胞到成熟精子分化过程中端粒组织的变化。讨论了体细胞和生精细胞在端粒核定位、蛋白质组成、DNA长度、端粒酶活性和染色质结构方面的异同。生殖系端粒的特殊特征可能对精子发生过程中端粒酶活性的调控、重组过程中同源染色体配对以及受精后雄原核发育和有序染色体撤离很重要。

相似文献

1
Telomeres in mammalian male germline cells.哺乳动物雄性生殖系细胞中的端粒。
Int Rev Cytol. 2002;218:37-67. doi: 10.1016/s0074-7696(02)18011-9.
2
Telomerase activity and telomere length in male germ cells.男性生殖细胞中的端粒酶活性与端粒长度
Biol Reprod. 2015 Feb;92(2):53. doi: 10.1095/biolreprod.114.124008. Epub 2015 Jan 7.
3
Telomere regulation and function during meiosis.减数分裂过程中的端粒调控与功能。
Chromosome Res. 2007;15(5):667-79. doi: 10.1007/s10577-007-1149-7.
4
Mammalian meiotic telomeres: composition and ultrastructure in telomerase-deficient mice.哺乳动物减数分裂端粒:端粒酶缺陷小鼠中的组成与超微结构
Eur J Cell Biol. 2002 Jun;81(6):335-40. doi: 10.1078/0171-9335-00259.
5
Centromere and telomere redistribution precedes homologue pairing and terminal synapsis initiation during prophase I of cattle spermatogenesis.在牛精子发生的减数分裂前期I,着丝粒和端粒重新分布先于同源染色体配对和末端联会起始。
Cytogenet Cell Genet. 2001;93(3-4):304-14. doi: 10.1159/000057002.
6
Telomere homeostasis in mammalian germ cells: a review.哺乳动物生殖细胞中的端粒稳态:综述
Chromosoma. 2016 Jun;125(2):337-51. doi: 10.1007/s00412-015-0555-4. Epub 2015 Nov 2.
7
Dynamic rearrangement of telomeres during spermatogenesis in mice.小鼠精子发生过程中端粒的动态重排。
Dev Biol. 2005 May 15;281(2):196-207. doi: 10.1016/j.ydbio.2005.02.025.
8
Telomeres and telomerase in human health and disease.端粒与端粒酶在人类健康和疾病中的作用
J Pediatr Endocrinol Metab. 2002 Mar;15(3):229-40. doi: 10.1515/jpem.2002.15.3.229.
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Telomeres, telomerase, and tumorigenesis--a review.端粒、端粒酶与肿瘤发生——综述
MedGenMed. 2004 Jul 26;6(3):19.
10
Telomere length in male germ cells is inversely correlated with telomerase activity.男性生殖细胞中的端粒长度与端粒酶活性呈负相关。
Biol Reprod. 2000 Aug;63(2):591-8. doi: 10.1095/biolreprod63.2.591.

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Male reproductive ageing: a radical road to ruin.男性生殖衰老:一条通向毁灭的激进之路。
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Impact of Advanced Paternal Age on Fertility and Risks of Genetic Disorders in Offspring.高龄父亲对生育能力和后代遗传疾病风险的影响。
Genes (Basel). 2023 Feb 14;14(2):486. doi: 10.3390/genes14020486.
3
Preferable location of chromosomes 1, 29, and X in bovine spermatozoa.牛精子中1号、29号和X染色体的优选定位。
AIMS Genet. 2018 Mar 21;5(2):113-123. doi: 10.3934/genet.2018.2.113. eCollection 2018.
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Cancer telomeres and white crows.癌症端粒与白乌鸦。
Am J Clin Exp Urol. 2018 Apr 1;6(2):93-100. eCollection 2018.
5
Sub-fertile sperm cells exemplify telomere dysfunction.亚生育力精子细胞是端粒功能障碍的例证。
J Assist Reprod Genet. 2018 Jan;35(1):143-148. doi: 10.1007/s10815-017-1029-9. Epub 2017 Sep 13.
6
Paternal and grandpaternal ages at conception and descendant telomere lengths in chimpanzees and humans.黑猩猩和人类受孕时的父系及祖父系年龄与后代端粒长度
Am J Phys Anthropol. 2017 Feb;162(2):201-207. doi: 10.1002/ajpa.23109. Epub 2016 Oct 12.
7
Altered Crossover Distribution and Frequency in Spermatocytes of Infertile Men with Azoospermia.无精子症不育男性精母细胞中交叉分布和频率的改变
PLoS One. 2016 Jun 6;11(6):e0156817. doi: 10.1371/journal.pone.0156817. eCollection 2016.
8
High telomerase is a hallmark of undifferentiated spermatogonia and is required for maintenance of male germline stem cells.高端粒酶是未分化精原细胞的一个标志,是维持雄性生殖系干细胞所必需的。
Genes Dev. 2015 Dec 1;29(23):2420-34. doi: 10.1101/gad.271783.115. Epub 2015 Nov 19.
9
Effects of increased paternal age on sperm quality, reproductive outcome and associated epigenetic risks to offspring.父亲年龄增加对精子质量、生殖结局及子代相关表观遗传风险的影响。
Reprod Biol Endocrinol. 2015 Apr 19;13:35. doi: 10.1186/s12958-015-0028-x.
10
Maternal and genetic factors determine early life telomere length.母亲和遗传因素决定生命早期的端粒长度。
Proc Biol Sci. 2015 Jan 22;282(1799):20142263. doi: 10.1098/rspb.2014.2263.