The GIY-YIG Type Endonuclease Ankyrin Repeat and LEM Domain-Containing Protein 1 (ANKLE1) Is Dispensable for Mouse Hematopoiesis
Ankyrin repeat and LEM-domain containing protein 1 (ANKLE1) is a GIY-YIG endonuclease with unknown functions, mainly expressed in mouse hematopoietic tissues. To test its potential role in hematopoiesis we generated Ankle1-deficient mice. Ankle1Δ/Δ mice are viable without any detectable phenotype in...
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description | Ankyrin repeat and LEM-domain containing protein 1 (ANKLE1) is a GIY-YIG endonuclease with unknown functions, mainly expressed in mouse hematopoietic tissues. To test its potential role in hematopoiesis we generated Ankle1-deficient mice. Ankle1Δ/Δ mice are viable without any detectable phenotype in hematopoiesis. Neither hematopoietic progenitor cells, myeloid and lymphoid progenitors, nor B and T cell development in bone marrow, spleen and thymus, are affected in Ankle1Δ/Δ-mice. Similarly embryonic stress erythropoiesis in liver and adult erythropoiesis in bone marrow and spleen appear normal. To test whether ANKLE1, like the only other known GIY-YIG endonuclease in mammals, SLX1, may contribute to Holliday junction resolution during DNA repair, Ankle1-deficient cells were exposed to various DNA-damage inducing agents. However, lack of Ankle1 did not affect cell viability and, unlike depletion of Slx1, Ankle1-deficiency did not increase sister chromatid exchange in Bloom helicase-depleted cells. Altogether, we show that lack of Ankle1 does neither affect mouse hematopoiesis nor DNA damage repair in mouse embryonic fibroblasts, indicating a redundant or non-essential function of ANKLE1 in mouse. |
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To test its potential role in hematopoiesis we generated Ankle1-deficient mice. Ankle1Δ/Δ mice are viable without any detectable phenotype in hematopoiesis. Neither hematopoietic progenitor cells, myeloid and lymphoid progenitors, nor B and T cell development in bone marrow, spleen and thymus, are affected in Ankle1Δ/Δ-mice. Similarly embryonic stress erythropoiesis in liver and adult erythropoiesis in bone marrow and spleen appear normal. To test whether ANKLE1, like the only other known GIY-YIG endonuclease in mammals, SLX1, may contribute to Holliday junction resolution during DNA repair, Ankle1-deficient cells were exposed to various DNA-damage inducing agents. However, lack of Ankle1 did not affect cell viability and, unlike depletion of Slx1, Ankle1-deficiency did not increase sister chromatid exchange in Bloom helicase-depleted cells. Altogether, we show that lack of Ankle1 does neither affect mouse hematopoiesis nor DNA damage repair in mouse embryonic fibroblasts, indicating a redundant or non-essential function of ANKLE1 in mouse.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0152278</identifier><identifier>PMID: 27010503</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animal tissues ; Animals ; Ankyrins ; Biochemistry ; Biology and Life Sciences ; Bone marrow ; Breast cancer ; Cells (biology) ; Deoxyribonucleic acid ; DNA ; DNA damage ; DNA helicase ; DNA repair ; Embryo fibroblasts ; Embryos ; Endonuclease ; Endonucleases - genetics ; Endonucleases - physiology ; Erythropoiesis ; Fibroblasts ; Flow Cytometry ; Gene expression ; Gene Knockdown Techniques ; Genetic aspects ; Genomes ; Hematopoiesis ; Hematopoiesis - physiology ; Hematopoietic stem cells ; Laboratories ; Liver ; Lymphocytes B ; Lymphocytes T ; Mammals ; Medicine and Health Sciences ; Mice ; Mice, Inbred C57BL ; Nucleases ; Perutz, Max ; Physiological aspects ; Polymorphism, Single Nucleotide ; Progenitor cells ; Proteins ; Repair ; Research and Analysis Methods ; RNA, Messenger - genetics ; Rodents ; Sister chromatid exchange ; Spleen ; Stem cells ; Thymus</subject><ispartof>PloS one, 2016-03, Vol.11 (3), p.e0152278-e0152278</ispartof><rights>COPYRIGHT 2016 Public Library of Science</rights><rights>2016 Braun et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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Altogether, we show that lack of Ankle1 does neither affect mouse hematopoiesis nor DNA damage repair in mouse embryonic fibroblasts, indicating a redundant or non-essential function of ANKLE1 in mouse.</description><subject>Animal tissues</subject><subject>Animals</subject><subject>Ankyrins</subject><subject>Biochemistry</subject><subject>Biology and Life Sciences</subject><subject>Bone marrow</subject><subject>Breast cancer</subject><subject>Cells (biology)</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA damage</subject><subject>DNA helicase</subject><subject>DNA repair</subject><subject>Embryo fibroblasts</subject><subject>Embryos</subject><subject>Endonuclease</subject><subject>Endonucleases - genetics</subject><subject>Endonucleases - physiology</subject><subject>Erythropoiesis</subject><subject>Fibroblasts</subject><subject>Flow Cytometry</subject><subject>Gene expression</subject><subject>Gene Knockdown Techniques</subject><subject>Genetic aspects</subject><subject>Genomes</subject><subject>Hematopoiesis</subject><subject>Hematopoiesis - 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genetics</topic><topic>Endonucleases - physiology</topic><topic>Erythropoiesis</topic><topic>Fibroblasts</topic><topic>Flow Cytometry</topic><topic>Gene expression</topic><topic>Gene Knockdown Techniques</topic><topic>Genetic aspects</topic><topic>Genomes</topic><topic>Hematopoiesis</topic><topic>Hematopoiesis - physiology</topic><topic>Hematopoietic stem cells</topic><topic>Laboratories</topic><topic>Liver</topic><topic>Lymphocytes B</topic><topic>Lymphocytes T</topic><topic>Mammals</topic><topic>Medicine and Health Sciences</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Nucleases</topic><topic>Perutz, Max</topic><topic>Physiological aspects</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Progenitor cells</topic><topic>Proteins</topic><topic>Repair</topic><topic>Research and Analysis Methods</topic><topic>RNA, Messenger - genetics</topic><topic>Rodents</topic><topic>Sister chromatid exchange</topic><topic>Spleen</topic><topic>Stem cells</topic><topic>Thymus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Braun, Juliane</creatorcontrib><creatorcontrib>Meixner, Arabella</creatorcontrib><creatorcontrib>Brachner, Andreas</creatorcontrib><creatorcontrib>Foisner, Roland</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Braun, Juliane</au><au>Meixner, Arabella</au><au>Brachner, Andreas</au><au>Foisner, Roland</au><au>Zhou, Zhongjun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The GIY-YIG Type Endonuclease Ankyrin Repeat and LEM Domain-Containing Protein 1 (ANKLE1) Is Dispensable for Mouse Hematopoiesis</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2016-03-24</date><risdate>2016</risdate><volume>11</volume><issue>3</issue><spage>e0152278</spage><epage>e0152278</epage><pages>e0152278-e0152278</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Ankyrin repeat and LEM-domain containing protein 1 (ANKLE1) is a GIY-YIG endonuclease with unknown functions, mainly expressed in mouse hematopoietic tissues. To test its potential role in hematopoiesis we generated Ankle1-deficient mice. Ankle1Δ/Δ mice are viable without any detectable phenotype in hematopoiesis. Neither hematopoietic progenitor cells, myeloid and lymphoid progenitors, nor B and T cell development in bone marrow, spleen and thymus, are affected in Ankle1Δ/Δ-mice. Similarly embryonic stress erythropoiesis in liver and adult erythropoiesis in bone marrow and spleen appear normal. To test whether ANKLE1, like the only other known GIY-YIG endonuclease in mammals, SLX1, may contribute to Holliday junction resolution during DNA repair, Ankle1-deficient cells were exposed to various DNA-damage inducing agents. However, lack of Ankle1 did not affect cell viability and, unlike depletion of Slx1, Ankle1-deficiency did not increase sister chromatid exchange in Bloom helicase-depleted cells. Altogether, we show that lack of Ankle1 does neither affect mouse hematopoiesis nor DNA damage repair in mouse embryonic fibroblasts, indicating a redundant or non-essential function of ANKLE1 in mouse.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>27010503</pmid><doi>10.1371/journal.pone.0152278</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animal tissues Animals Ankyrins Biochemistry Biology and Life Sciences Bone marrow Breast cancer Cells (biology) Deoxyribonucleic acid DNA DNA damage DNA helicase DNA repair Embryo fibroblasts Embryos Endonuclease Endonucleases - genetics Endonucleases - physiology Erythropoiesis Fibroblasts Flow Cytometry Gene expression Gene Knockdown Techniques Genetic aspects Genomes Hematopoiesis Hematopoiesis - physiology Hematopoietic stem cells Laboratories Liver Lymphocytes B Lymphocytes T Mammals Medicine and Health Sciences Mice Mice, Inbred C57BL Nucleases Perutz, Max Physiological aspects Polymorphism, Single Nucleotide Progenitor cells Proteins Repair Research and Analysis Methods RNA, Messenger - genetics Rodents Sister chromatid exchange Spleen Stem cells Thymus |
title | The GIY-YIG Type Endonuclease Ankyrin Repeat and LEM Domain-Containing Protein 1 (ANKLE1) Is Dispensable for Mouse Hematopoiesis |
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