Cutting Edge: Check Your Mice-A Point Mutation in the Ncr1 Locus Identified in CD45.1 Congenic Mice with Consequences in Mouse Susceptibility to Infection
B6.SJL- /Boy (CD45.1) mice have been used in hundreds of congenic competitive transplants, with the presumption that they differ from C57BL/6 mice only at the CD45 locus. In this study, we describe a point mutation in the natural cytotoxicity receptor 1 ( ) locus fortuitously identified in the CD45....
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Veröffentlicht in: | The Journal of immunology (1950) 2018-03, Vol.200 (6), p.1982-1987 |
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container_end_page | 1987 |
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container_issue | 6 |
container_start_page | 1982 |
container_title | The Journal of immunology (1950) |
container_volume | 200 |
creator | Jang, Youngsoon Gerbec, Zachary J Won, Taejoon Choi, Bongkum Podsiad, Amy B Moore, Bethany Malarkannan, Subramaniam Laouar, Yasmina |
description | B6.SJL-
/Boy (CD45.1) mice have been used in hundreds of congenic competitive transplants, with the presumption that they differ from C57BL/6 mice only at the CD45 locus. In this study, we describe a point mutation in the natural cytotoxicity receptor 1 (
) locus fortuitously identified in the CD45.1 strain. This point mutation was mapped at the 40th nucleotide of the
locus causing a single amino acid mutation from cysteine to arginine at position 14 from the start codon, resulting in loss of NCR1 expression. We found that these mice were more resistant to CMV due to a hyper innate IFN-γ response in the absence of NCR1. In contrast, loss of NCR1 increased susceptibility to influenza virus, a result that is consistent with the role of NCR1 in the recognition of influenza Ag, hemagglutinin. This work sheds light on potential confounding experimental interpretation when this congenic strain is used as a tool for tracking lymphocyte development. |
doi_str_mv | 10.4049/jimmunol.1701676 |
format | Article |
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/Boy (CD45.1) mice have been used in hundreds of congenic competitive transplants, with the presumption that they differ from C57BL/6 mice only at the CD45 locus. In this study, we describe a point mutation in the natural cytotoxicity receptor 1 (
) locus fortuitously identified in the CD45.1 strain. This point mutation was mapped at the 40th nucleotide of the
locus causing a single amino acid mutation from cysteine to arginine at position 14 from the start codon, resulting in loss of NCR1 expression. We found that these mice were more resistant to CMV due to a hyper innate IFN-γ response in the absence of NCR1. In contrast, loss of NCR1 increased susceptibility to influenza virus, a result that is consistent with the role of NCR1 in the recognition of influenza Ag, hemagglutinin. This work sheds light on potential confounding experimental interpretation when this congenic strain is used as a tool for tracking lymphocyte development.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.1701676</identifier><identifier>PMID: 29440507</identifier><language>eng</language><publisher>United States: American Association of Immunologists</publisher><subject>Amino acids ; Animals ; Antigens, Ly - genetics ; Arginine ; CD45 antigen ; Cytotoxicity ; Hemagglutinins ; Hemagglutinins - immunology ; Immunity, Innate ; Influenza ; Interferon-gamma - immunology ; Leukocyte Common Antigens - genetics ; Mice ; Mice, Congenic ; Mice, Inbred C57BL ; Mutation ; Natural Cytotoxicity Triggering Receptor 1 - genetics ; Orthomyxoviridae - immunology ; Orthomyxoviridae Infections - genetics ; Orthomyxoviridae Infections - immunology ; Point mutation ; Point Mutation - genetics ; Viruses ; γ-Interferon</subject><ispartof>The Journal of immunology (1950), 2018-03, Vol.200 (6), p.1982-1987</ispartof><rights>Copyright © 2018 by The American Association of Immunologists, Inc.</rights><rights>Copyright American Association of Immunologists Mar 15, 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c369t-6b8e9334a3a702d778f201f6e64bfb586e08c182c52826382c7853b3e437ce2f3</citedby><cites>FETCH-LOGICAL-c369t-6b8e9334a3a702d778f201f6e64bfb586e08c182c52826382c7853b3e437ce2f3</cites><orcidid>0000-0001-5968-2016 ; 0000-0002-8865-4791 ; 0000-0003-3051-745X ; 0000-0002-6134-4291</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29440507$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jang, Youngsoon</creatorcontrib><creatorcontrib>Gerbec, Zachary J</creatorcontrib><creatorcontrib>Won, Taejoon</creatorcontrib><creatorcontrib>Choi, Bongkum</creatorcontrib><creatorcontrib>Podsiad, Amy</creatorcontrib><creatorcontrib>B Moore, Bethany</creatorcontrib><creatorcontrib>Malarkannan, Subramaniam</creatorcontrib><creatorcontrib>Laouar, Yasmina</creatorcontrib><title>Cutting Edge: Check Your Mice-A Point Mutation in the Ncr1 Locus Identified in CD45.1 Congenic Mice with Consequences in Mouse Susceptibility to Infection</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>B6.SJL-
/Boy (CD45.1) mice have been used in hundreds of congenic competitive transplants, with the presumption that they differ from C57BL/6 mice only at the CD45 locus. In this study, we describe a point mutation in the natural cytotoxicity receptor 1 (
) locus fortuitously identified in the CD45.1 strain. This point mutation was mapped at the 40th nucleotide of the
locus causing a single amino acid mutation from cysteine to arginine at position 14 from the start codon, resulting in loss of NCR1 expression. We found that these mice were more resistant to CMV due to a hyper innate IFN-γ response in the absence of NCR1. In contrast, loss of NCR1 increased susceptibility to influenza virus, a result that is consistent with the role of NCR1 in the recognition of influenza Ag, hemagglutinin. This work sheds light on potential confounding experimental interpretation when this congenic strain is used as a tool for tracking lymphocyte development.</description><subject>Amino acids</subject><subject>Animals</subject><subject>Antigens, Ly - genetics</subject><subject>Arginine</subject><subject>CD45 antigen</subject><subject>Cytotoxicity</subject><subject>Hemagglutinins</subject><subject>Hemagglutinins - immunology</subject><subject>Immunity, Innate</subject><subject>Influenza</subject><subject>Interferon-gamma - immunology</subject><subject>Leukocyte Common Antigens - genetics</subject><subject>Mice</subject><subject>Mice, Congenic</subject><subject>Mice, Inbred C57BL</subject><subject>Mutation</subject><subject>Natural Cytotoxicity Triggering Receptor 1 - genetics</subject><subject>Orthomyxoviridae - immunology</subject><subject>Orthomyxoviridae Infections - genetics</subject><subject>Orthomyxoviridae Infections - immunology</subject><subject>Point mutation</subject><subject>Point Mutation - genetics</subject><subject>Viruses</subject><subject>γ-Interferon</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU-P0zAQxS0EYkvhzglZ4rKXlPGf2Cm3VVigUrsgAQdOUeJMWpfELrGj1X6V_bQ4bJcDkqWxPG-en-ZHyGsGKwly_e5oh2Fyvl8xDUxp9YQsWJ5DphSop2QBwHnGtNIX5EUIRwBQwOVzcsHXUkIOekHuyylG6_b0ut3je1oe0PyiP_000p01mF3Rr966SHdTrKP1jlpH4wHpjRkZ3XozBbpp0UXbWWznZvlB5itGS-_26Kz560JvbTzMTwF_T-gMhlm581NA-m0KBk_RNra38Y5GTzeuQzP_9ZI86-o-4KtzXZIfH6-_l5-z7ZdPm_Jqmxmh1jFTTYFrIWQtag281broOLBOoZJN1-SFQigMK7jJecGVSBdd5KIRKIU2yDuxJJcPvqfRp3whVoNNofq-dpgyVnxeI1MinSV5-5_0mFblUrqkYkxCgsKSCh5UZvQhjNhVp9EO9XhXMahmbtUjt-rMLY28ORtPzYDtv4FHUOIPrWSUDg</recordid><startdate>20180315</startdate><enddate>20180315</enddate><creator>Jang, Youngsoon</creator><creator>Gerbec, Zachary J</creator><creator>Won, Taejoon</creator><creator>Choi, Bongkum</creator><creator>Podsiad, Amy</creator><creator>B Moore, Bethany</creator><creator>Malarkannan, Subramaniam</creator><creator>Laouar, Yasmina</creator><general>American Association of Immunologists</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5968-2016</orcidid><orcidid>https://orcid.org/0000-0002-8865-4791</orcidid><orcidid>https://orcid.org/0000-0003-3051-745X</orcidid><orcidid>https://orcid.org/0000-0002-6134-4291</orcidid></search><sort><creationdate>20180315</creationdate><title>Cutting Edge: Check Your Mice-A Point Mutation in the Ncr1 Locus Identified in CD45.1 Congenic Mice with Consequences in Mouse Susceptibility to Infection</title><author>Jang, Youngsoon ; Gerbec, Zachary J ; Won, Taejoon ; Choi, Bongkum ; Podsiad, Amy ; B Moore, Bethany ; Malarkannan, Subramaniam ; Laouar, Yasmina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c369t-6b8e9334a3a702d778f201f6e64bfb586e08c182c52826382c7853b3e437ce2f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Amino acids</topic><topic>Animals</topic><topic>Antigens, Ly - genetics</topic><topic>Arginine</topic><topic>CD45 antigen</topic><topic>Cytotoxicity</topic><topic>Hemagglutinins</topic><topic>Hemagglutinins - immunology</topic><topic>Immunity, Innate</topic><topic>Influenza</topic><topic>Interferon-gamma - immunology</topic><topic>Leukocyte Common Antigens - genetics</topic><topic>Mice</topic><topic>Mice, Congenic</topic><topic>Mice, Inbred C57BL</topic><topic>Mutation</topic><topic>Natural Cytotoxicity Triggering Receptor 1 - genetics</topic><topic>Orthomyxoviridae - immunology</topic><topic>Orthomyxoviridae Infections - genetics</topic><topic>Orthomyxoviridae Infections - immunology</topic><topic>Point mutation</topic><topic>Point Mutation - genetics</topic><topic>Viruses</topic><topic>γ-Interferon</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jang, Youngsoon</creatorcontrib><creatorcontrib>Gerbec, Zachary J</creatorcontrib><creatorcontrib>Won, Taejoon</creatorcontrib><creatorcontrib>Choi, Bongkum</creatorcontrib><creatorcontrib>Podsiad, Amy</creatorcontrib><creatorcontrib>B Moore, Bethany</creatorcontrib><creatorcontrib>Malarkannan, Subramaniam</creatorcontrib><creatorcontrib>Laouar, Yasmina</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jang, Youngsoon</au><au>Gerbec, Zachary J</au><au>Won, Taejoon</au><au>Choi, Bongkum</au><au>Podsiad, Amy</au><au>B Moore, Bethany</au><au>Malarkannan, Subramaniam</au><au>Laouar, Yasmina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cutting Edge: Check Your Mice-A Point Mutation in the Ncr1 Locus Identified in CD45.1 Congenic Mice with Consequences in Mouse Susceptibility to Infection</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>2018-03-15</date><risdate>2018</risdate><volume>200</volume><issue>6</issue><spage>1982</spage><epage>1987</epage><pages>1982-1987</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><abstract>B6.SJL-
/Boy (CD45.1) mice have been used in hundreds of congenic competitive transplants, with the presumption that they differ from C57BL/6 mice only at the CD45 locus. In this study, we describe a point mutation in the natural cytotoxicity receptor 1 (
) locus fortuitously identified in the CD45.1 strain. This point mutation was mapped at the 40th nucleotide of the
locus causing a single amino acid mutation from cysteine to arginine at position 14 from the start codon, resulting in loss of NCR1 expression. We found that these mice were more resistant to CMV due to a hyper innate IFN-γ response in the absence of NCR1. In contrast, loss of NCR1 increased susceptibility to influenza virus, a result that is consistent with the role of NCR1 in the recognition of influenza Ag, hemagglutinin. This work sheds light on potential confounding experimental interpretation when this congenic strain is used as a tool for tracking lymphocyte development.</abstract><cop>United States</cop><pub>American Association of Immunologists</pub><pmid>29440507</pmid><doi>10.4049/jimmunol.1701676</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0001-5968-2016</orcidid><orcidid>https://orcid.org/0000-0002-8865-4791</orcidid><orcidid>https://orcid.org/0000-0003-3051-745X</orcidid><orcidid>https://orcid.org/0000-0002-6134-4291</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Alma/SFX Local Collection; EZB Electronic Journals Library |
subjects | Amino acids Animals Antigens, Ly - genetics Arginine CD45 antigen Cytotoxicity Hemagglutinins Hemagglutinins - immunology Immunity, Innate Influenza Interferon-gamma - immunology Leukocyte Common Antigens - genetics Mice Mice, Congenic Mice, Inbred C57BL Mutation Natural Cytotoxicity Triggering Receptor 1 - genetics Orthomyxoviridae - immunology Orthomyxoviridae Infections - genetics Orthomyxoviridae Infections - immunology Point mutation Point Mutation - genetics Viruses γ-Interferon |
title | Cutting Edge: Check Your Mice-A Point Mutation in the Ncr1 Locus Identified in CD45.1 Congenic Mice with Consequences in Mouse Susceptibility to Infection |
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