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Mouse CCDC79 (TERB1) is a meiosis-specific telomere associated protein

BACKGROUND: Telomeres have crucial meiosis-specific roles in the orderly reduction of chromosome numbers and in ensuring the integrity of the genome during meiosis. One such role is the attachment of telomeres to trans-nuclear envelope protein complexes that connect telomeres to motor proteins in th...

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Autores principales: Daniel, Katrin, Tränkner, Daniel, Wojtasz, Lukasz, Shibuya, Hiroki, Watanabe, Yoshinori, Alsheimer, Manfred, Tóth, Attila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4038382/
https://www.ncbi.nlm.nih.gov/pubmed/24885367
http://dx.doi.org/10.1186/1471-2121-15-17
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author Daniel, Katrin
Tränkner, Daniel
Wojtasz, Lukasz
Shibuya, Hiroki
Watanabe, Yoshinori
Alsheimer, Manfred
Tóth, Attila
author_facet Daniel, Katrin
Tränkner, Daniel
Wojtasz, Lukasz
Shibuya, Hiroki
Watanabe, Yoshinori
Alsheimer, Manfred
Tóth, Attila
author_sort Daniel, Katrin
collection PubMed
description BACKGROUND: Telomeres have crucial meiosis-specific roles in the orderly reduction of chromosome numbers and in ensuring the integrity of the genome during meiosis. One such role is the attachment of telomeres to trans-nuclear envelope protein complexes that connect telomeres to motor proteins in the cytoplasm. These trans-nuclear envelope connections between telomeres and cytoplasmic motor proteins permit the active movement of telomeres and chromosomes during the first meiotic prophase. Movements of chromosomes/telomeres facilitate the meiotic recombination process, and allow high fidelity pairing of homologous chromosomes. Pairing of homologous chromosomes is a prerequisite for their correct segregation during the first meiotic division. Although inner-nuclear envelope proteins, such as SUN1 and potentially SUN2, are known to bind and recruit meiotic telomeres, these proteins are not meiosis-specific, therefore cannot solely account for telomere-nuclear envelope attachment and/or for other meiosis-specific characteristics of telomeres in mammals. RESULTS: We identify CCDC79, alternatively named TERB1, as a meiosis-specific protein that localizes to telomeres from leptotene to diplotene stages of the first meiotic prophase. CCDC79 and SUN1 associate with telomeres almost concurrently at the onset of prophase, indicating a possible role for CCDC79 in telomere-nuclear envelope interactions and/or telomere movements. Consistent with this scenario, CCDC79 is missing from most telomeres that fail to connect to SUN1 protein in spermatocytes lacking the meiosis-specific cohesin SMC1B. SMC1B-deficient spermatocytes display both reduced efficiency in telomere-nuclear envelope attachment and reduced stability of telomeres specifically during meiotic prophase. Importantly, CCDC79 associates with telomeres in SUN1-deficient spermatocytes, which strongly indicates that localization of CCDC79 to telomeres does not require telomere-nuclear envelope attachment. CONCLUSION: CCDC79 is a meiosis-specific telomere associated protein. Based on our findings we propose that CCDC79 plays a role in meiosis-specific telomere functions. In particular, we favour the possibility that CCDC79 is involved in telomere-nuclear envelope attachment and/or the stabilization of meiotic telomeres. These conclusions are consistent with the findings of an independently initiated study that analysed CCDC79/TERB1 functions.
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spelling pubmed-40383822014-05-30 Mouse CCDC79 (TERB1) is a meiosis-specific telomere associated protein Daniel, Katrin Tränkner, Daniel Wojtasz, Lukasz Shibuya, Hiroki Watanabe, Yoshinori Alsheimer, Manfred Tóth, Attila BMC Cell Biol Research Article BACKGROUND: Telomeres have crucial meiosis-specific roles in the orderly reduction of chromosome numbers and in ensuring the integrity of the genome during meiosis. One such role is the attachment of telomeres to trans-nuclear envelope protein complexes that connect telomeres to motor proteins in the cytoplasm. These trans-nuclear envelope connections between telomeres and cytoplasmic motor proteins permit the active movement of telomeres and chromosomes during the first meiotic prophase. Movements of chromosomes/telomeres facilitate the meiotic recombination process, and allow high fidelity pairing of homologous chromosomes. Pairing of homologous chromosomes is a prerequisite for their correct segregation during the first meiotic division. Although inner-nuclear envelope proteins, such as SUN1 and potentially SUN2, are known to bind and recruit meiotic telomeres, these proteins are not meiosis-specific, therefore cannot solely account for telomere-nuclear envelope attachment and/or for other meiosis-specific characteristics of telomeres in mammals. RESULTS: We identify CCDC79, alternatively named TERB1, as a meiosis-specific protein that localizes to telomeres from leptotene to diplotene stages of the first meiotic prophase. CCDC79 and SUN1 associate with telomeres almost concurrently at the onset of prophase, indicating a possible role for CCDC79 in telomere-nuclear envelope interactions and/or telomere movements. Consistent with this scenario, CCDC79 is missing from most telomeres that fail to connect to SUN1 protein in spermatocytes lacking the meiosis-specific cohesin SMC1B. SMC1B-deficient spermatocytes display both reduced efficiency in telomere-nuclear envelope attachment and reduced stability of telomeres specifically during meiotic prophase. Importantly, CCDC79 associates with telomeres in SUN1-deficient spermatocytes, which strongly indicates that localization of CCDC79 to telomeres does not require telomere-nuclear envelope attachment. CONCLUSION: CCDC79 is a meiosis-specific telomere associated protein. Based on our findings we propose that CCDC79 plays a role in meiosis-specific telomere functions. In particular, we favour the possibility that CCDC79 is involved in telomere-nuclear envelope attachment and/or the stabilization of meiotic telomeres. These conclusions are consistent with the findings of an independently initiated study that analysed CCDC79/TERB1 functions. BioMed Central 2014-05-22 /pmc/articles/PMC4038382/ /pubmed/24885367 http://dx.doi.org/10.1186/1471-2121-15-17 Text en Copyright © 2014 Daniel et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Daniel, Katrin
Tränkner, Daniel
Wojtasz, Lukasz
Shibuya, Hiroki
Watanabe, Yoshinori
Alsheimer, Manfred
Tóth, Attila
Mouse CCDC79 (TERB1) is a meiosis-specific telomere associated protein
title Mouse CCDC79 (TERB1) is a meiosis-specific telomere associated protein
title_full Mouse CCDC79 (TERB1) is a meiosis-specific telomere associated protein
title_fullStr Mouse CCDC79 (TERB1) is a meiosis-specific telomere associated protein
title_full_unstemmed Mouse CCDC79 (TERB1) is a meiosis-specific telomere associated protein
title_short Mouse CCDC79 (TERB1) is a meiosis-specific telomere associated protein
title_sort mouse ccdc79 (terb1) is a meiosis-specific telomere associated protein
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4038382/
https://www.ncbi.nlm.nih.gov/pubmed/24885367
http://dx.doi.org/10.1186/1471-2121-15-17
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