Check your mice: a point mutation in the Ncr1 locus identified in CD45.1 congenic mice with consequences on mouse susceptibility to infection
B6.SJL-Ptprc a Pepc b /Boy (CD45.1) mice have been used in hundreds of congenic competitive transplants, with the presumption that they differ from B6 mice only at the CD45 locus. In this study, we describe a point mutation in the Ncr1 locus fortuitously identified in the CD45.1 strain. This point m...
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Veröffentlicht in: | The Journal of immunology (1950) 2018-02, 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 Moore, Bethany Malarkannan, Subramaniam Laouar, Yasmina |
description | B6.SJL-Ptprc
a
Pepc
b
/Boy (CD45.1) mice have been used in hundreds of congenic competitive transplants, with the presumption that they differ from B6 mice only at the CD45 locus. In this study, we describe a point mutation in the
Ncr1
locus fortuitously identified in the CD45.1 strain. This point mutation was mapped at the 40
th
nucleotide of the
Ncr1
locus causing a single amino acid mutation from cysteine to arginine at position 14 from start codon, resulting in loss of NCR1 expression. We found that these mice were more resistant to cytomegalovirus due to a hyper innate IFNγ response in the absence of NCR1. In contrast, loss of NCR1 increased susceptibility to Influenza virus, a result which is consistent with the role of NCR1 in the recognition of influenza antigen, hemagglutinin. This work shed light on potential confounding experimental interpretation if 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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a
Pepc
b
/Boy (CD45.1) mice have been used in hundreds of congenic competitive transplants, with the presumption that they differ from B6 mice only at the CD45 locus. In this study, we describe a point mutation in the
Ncr1
locus fortuitously identified in the CD45.1 strain. This point mutation was mapped at the 40
th
nucleotide of the
Ncr1
locus causing a single amino acid mutation from cysteine to arginine at position 14 from start codon, resulting in loss of NCR1 expression. We found that these mice were more resistant to cytomegalovirus due to a hyper innate IFNγ response in the absence of NCR1. In contrast, loss of NCR1 increased susceptibility to Influenza virus, a result which is consistent with the role of NCR1 in the recognition of influenza antigen, hemagglutinin. This work shed light on potential confounding experimental interpretation if 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><ispartof>The Journal of immunology (1950), 2018-02, Vol.200 (6), p.1982-1987</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids></links><search><creatorcontrib>Jang, Youngsoon</creatorcontrib><creatorcontrib>Gerbec, Zachary J.</creatorcontrib><creatorcontrib>Won, Taejoon</creatorcontrib><creatorcontrib>Choi, Bongkum</creatorcontrib><creatorcontrib>Podsiad, Amy</creatorcontrib><creatorcontrib>Moore, Bethany</creatorcontrib><creatorcontrib>Malarkannan, Subramaniam</creatorcontrib><creatorcontrib>Laouar, Yasmina</creatorcontrib><title>Check your mice: a point mutation in the Ncr1 locus identified in CD45.1 congenic mice with consequences on mouse susceptibility to infection</title><title>The Journal of immunology (1950)</title><description>B6.SJL-Ptprc
a
Pepc
b
/Boy (CD45.1) mice have been used in hundreds of congenic competitive transplants, with the presumption that they differ from B6 mice only at the CD45 locus. In this study, we describe a point mutation in the
Ncr1
locus fortuitously identified in the CD45.1 strain. This point mutation was mapped at the 40
th
nucleotide of the
Ncr1
locus causing a single amino acid mutation from cysteine to arginine at position 14 from start codon, resulting in loss of NCR1 expression. We found that these mice were more resistant to cytomegalovirus due to a hyper innate IFNγ response in the absence of NCR1. In contrast, loss of NCR1 increased susceptibility to Influenza virus, a result which is consistent with the role of NCR1 in the recognition of influenza antigen, hemagglutinin. This work shed light on potential confounding experimental interpretation if this congenic strain is used as a tool for tracking lymphocyte development.</description><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqljb1OwzAURi0EouFnZ7wvkHIdHIcysAQQExN7lLq3zS2xHWIblIfgnWkQCzPTJ31HOkeIK4lLhWp1vWdrk_P9UlYodaWPRCbLEnOtUR-LDLEoclnpaiHOQtgjosZCnYpFsVIKS6wy8VV3ZN5g8mkEy4buoIXBs4tgU2wjewfsIHYEL2aU0HuTAvCGXOQt02aG9YMqlxKMdztybH408Mmxm69A74mcoQAHk_UpEIQUDA2R19xznCD6g2RLZm5diJNt2we6_N1zcf_0-Fo_50NaW9qYQ3Zs-2YY2bbj1PiWm7_Ecdfs_EdT3ipEWd78W_AN9SZ1Xw</recordid><startdate>20180209</startdate><enddate>20180209</enddate><creator>Jang, Youngsoon</creator><creator>Gerbec, Zachary J.</creator><creator>Won, Taejoon</creator><creator>Choi, Bongkum</creator><creator>Podsiad, Amy</creator><creator>Moore, Bethany</creator><creator>Malarkannan, Subramaniam</creator><creator>Laouar, Yasmina</creator><scope>5PM</scope></search><sort><creationdate>20180209</creationdate><title>Check your mice: a point mutation in the Ncr1 locus identified in CD45.1 congenic mice with consequences on mouse susceptibility to infection</title><author>Jang, Youngsoon ; Gerbec, Zachary J. ; Won, Taejoon ; Choi, Bongkum ; Podsiad, Amy ; Moore, Bethany ; Malarkannan, Subramaniam ; Laouar, Yasmina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_58400153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><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>Moore, Bethany</creatorcontrib><creatorcontrib>Malarkannan, Subramaniam</creatorcontrib><creatorcontrib>Laouar, Yasmina</creatorcontrib><collection>PubMed Central (Full Participant titles)</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>Moore, Bethany</au><au>Malarkannan, Subramaniam</au><au>Laouar, Yasmina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Check your mice: a point mutation in the Ncr1 locus identified in CD45.1 congenic mice with consequences on mouse susceptibility to infection</atitle><jtitle>The Journal of immunology (1950)</jtitle><date>2018-02-09</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-Ptprc
a
Pepc
b
/Boy (CD45.1) mice have been used in hundreds of congenic competitive transplants, with the presumption that they differ from B6 mice only at the CD45 locus. In this study, we describe a point mutation in the
Ncr1
locus fortuitously identified in the CD45.1 strain. This point mutation was mapped at the 40
th
nucleotide of the
Ncr1
locus causing a single amino acid mutation from cysteine to arginine at position 14 from start codon, resulting in loss of NCR1 expression. We found that these mice were more resistant to cytomegalovirus due to a hyper innate IFNγ response in the absence of NCR1. In contrast, loss of NCR1 increased susceptibility to Influenza virus, a result which is consistent with the role of NCR1 in the recognition of influenza antigen, hemagglutinin. This work shed light on potential confounding experimental interpretation if this congenic strain is used as a tool for tracking lymphocyte development.</abstract><pmid>29440507</pmid><doi>10.4049/jimmunol.1701676</doi></addata></record> |
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title | Check your mice: a point mutation in the Ncr1 locus identified in CD45.1 congenic mice with consequences on mouse susceptibility to infection |
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