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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mir148atm2942.1Arte
targeted mutation 2942.1, TaconicArtemis
MGI:6720859
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Mir148atm2942.1Arte/Mir148atm2942.1Arte
Cd19tm1(cre)Cgn/Cd19+
involves: 129P2/OlaHsd * C57BL/6 MGI:6731079
cn2
Mir148atm2942.1Arte/Mir148atm2942.1Arte
Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+
involves: C57BL/6 * C57BL/6NTac MGI:6731094


Genotype
MGI:6731079
cn1
Allelic
Composition
Mir148atm2942.1Arte/Mir148atm2942.1Arte
Cd19tm1(cre)Cgn/Cd19+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cd19tm1(cre)Cgn mutation (11 available); any Cd19 mutation (60 available)
Mir148atm2942.1Arte mutation (0 available); any Mir148a mutation (5 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• a reduction between 30 and 50% in IgA-secreting cells in spleen and bone marrow
• a reduction between 30 and 50% in IgG-secreting cells in the bone marrow
• marker analysis shows a 50% reduction of splenic CD138/Taci+ plasmablast/plasma cell numbers; this decrease is attributed to the approximate 60% decrease in the late CD19-negative mature plasma cell subset
• the number of late CD19-negative P3-plasma cells is reduced in the bone marrow by approximately 50%, but only in the Taci+ plasma cell subset with a high abundance of surface CD138
• 42 days after NP-KLH immunization, mice show a trend of increased numbers of NP-specific memory B cells (CD38-sIgG+) cells in the spleen and bone marrow
• numbers of pro-B cells, pre-B cells, immature B cells, and recirculating mature B cells in the bone marrow are unaltered in non-immunized mice
• differentiation of germinal center B cells into plasmablasts is impaired resulting in a decrease in numbers of newly formed plasmablasts after immunization with NP-KLH
• however, the number of germinal center B cells is not altered
• serum IgA levels are reduced by roughly 50% in non-immunized mice
• serum IgG levels are reduced by roughly 50% in non-immunized mice
• mice immunized with the thymus-dependent model antigen TNP-KLH show reduced TNP-specific IgG titers
• serum IgM levels are reduced by roughly 50% in non-immunized mice
• mice show reduced antigen-specific antibody responses
• TNP-KLH-immunized mice show a 50% reduction in the number of TNP-specific IgG- or IgM-secreting cells in the spleen and bone marrow 70 days after primary immunization
• TNP-KLH-immunized mice show a reduction in the CD138/Taci+ plasmablast/plasma cell population in the spleen and bone marrow, indicating fewer mature P3-plasma cells
• however, the number of P1-plasmablasts and P2-plasma cells in the spleen and bone marrow are not reduced in TNP-KLH-immunized mice
• mice show lower numbers of P1-plasmablasts in the blood 14 days after primary immunization with TNP-KLH
• TNP-KLH immunized mice show a more pronounced shift to CD19+ cells in CD138/Taci+ populations under homeostatic conditions
• the number of CD138low early P2-plasma cells in the bone marrow is elevated in TNP-KLH immunized mice

hematopoietic system
• a reduction between 30 and 50% in IgA-secreting cells in spleen and bone marrow
• a reduction between 30 and 50% in IgG-secreting cells in the bone marrow
• marker analysis shows a 50% reduction of splenic CD138/Taci+ plasmablast/plasma cell numbers; this decrease is attributed to the approximate 60% decrease in the late CD19-negative mature plasma cell subset
• the number of late CD19-negative P3-plasma cells is reduced in the bone marrow by approximately 50%, but only in the Taci+ plasma cell subset with a high abundance of surface CD138
• 42 days after NP-KLH immunization, mice show a trend of increased numbers of NP-specific memory B cells (CD38-sIgG+) cells in the spleen and bone marrow
• numbers of pro-B cells, pre-B cells, immature B cells, and recirculating mature B cells in the bone marrow are unaltered in non-immunized mice
• differentiation of germinal center B cells into plasmablasts is impaired resulting in a decrease in numbers of newly formed plasmablasts after immunization with NP-KLH
• however, the number of germinal center B cells is not altered
• serum IgA levels are reduced by roughly 50% in non-immunized mice
• serum IgG levels are reduced by roughly 50% in non-immunized mice
• mice immunized with the thymus-dependent model antigen TNP-KLH show reduced TNP-specific IgG titers
• serum IgM levels are reduced by roughly 50% in non-immunized mice




Genotype
MGI:6731094
cn2
Allelic
Composition
Mir148atm2942.1Arte/Mir148atm2942.1Arte
Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+
Genetic
Background
involves: C57BL/6 * C57BL/6NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm9(cre/ESR1)Arte mutation (2 available); any Gt(ROSA)26Sor mutation (993 available)
Mir148atm2942.1Arte mutation (0 available); any Mir148a mutation (5 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• reduction in the number of mature resting plasma cells in the bone marrow following immunization with TNP-KLH and treatment with tamoxifen
• the number of P3-plasma cells in the blood in elevated in TNP-KLH immunized and boosted mice treated with tamoxifen
• the number of P1-plasmablasts is diminished in the spleen in TNP-KLH immunized and boosted mice treated with tamoxifen
• reduction in EdU+ mature P3-plasma cells in the bone marrow of TNP-KLH immunized and tamoxifen treated mice indicating reduced mature plasma turnover
• however, the EdU+ P2-plasma cell subset is unchanged

immune system
• reduction in the number of mature resting plasma cells in the bone marrow following immunization with TNP-KLH and treatment with tamoxifen
• the number of P3-plasma cells in the blood in elevated in TNP-KLH immunized and boosted mice treated with tamoxifen
• the number of P1-plasmablasts is diminished in the spleen in TNP-KLH immunized and boosted mice treated with tamoxifen
• reduction in EdU+ mature P3-plasma cells in the bone marrow of TNP-KLH immunized and tamoxifen treated mice indicating reduced mature plasma turnover
• however, the EdU+ P2-plasma cell subset is unchanged
• mice immunized and boosted with TNP-KLH and treated with tamoxifen exhibit a reduction in the CD138/Taci+ plasmablast/plasma cell population, notably the CD19-negative mature resting P3-plasma cells in the spleen and bone marrow
• mice immunized and boosted with TNP-KLH and treated with tamoxifen show a decrease in total number of antibody secreting cells in the bone marrow
• however, the numbers of NTP-specific antibody secreting in the spleen and bone marrow remain unchanged after tamoxifen treatment





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory