| First Author | Côrte-Real J | Year | 2009 |
| Journal | Genes Immun | Volume | 10 |
| Issue | 1 | Pages | 93-9 |
| PubMed ID | 18818690 | Mgi Jnum | J:153393 |
| Mgi Id | MGI:4365337 | Doi | 10.1038/gene.2008.73 |
| Citation | Corte-Real J, et al. (2009) Irf4 is a positional and functional candidate gene for the control of serum IgM levels in the mouse. Genes Immun 10(1):93-9 |
| abstractText | Natural IgM are involved in numerous immunological functions but the genetic factors that control the homeostasis of its secretion and upholding remain unknown. Prompted by the finding that C57BL/6 mice had significantly lower serum levels of IgM when compared with BALB/c mice, we performed a genome-wide screen and found that the level of serum IgM was controlled by a QTL on chromosome 13 reaching the highest level of association at marker D13Mit266 (LOD score=3.54). This locus was named IgMSC1 and covered a region encompassing the interferon-regulatory factor 4 gene (Irf4). The number of splenic mature B cells in C57BL/6 did not differ from BALB/c mice but we found that low serum levels of IgM in C57BL/6 mice correlated with lower frequency of IgM-secreting cells in the spleen and in the peritoneal cavity. These results suggested that C57BL/6 mice have lower efficiency in late B-cell maturation, a process that is highly impaired in Irf4 knockout mice. In fact, we also found reduced Irf4 gene expression in B cells of C57BL/6 mice. Thus, we propose Irf4 as a candidate for the IgMSC1 locus, which controls IgM homeostatic levels at the level of B-cell terminal differentiation. |
