| First Author | Martin OA | Year | 2023 |
| Journal | Front Immunol | Volume | 14 |
| Pages | 1030813 | PubMed ID | 36865553 |
| Mgi Jnum | J:342746 | Mgi Id | MGI:7440648 |
| Doi | 10.3389/fimmu.2023.1030813 | Citation | Martin OA, et al. (2023) The IgH Emicro-MAR regions promote UNG-dependent error-prone repair to optimize somatic hypermutation. Front Immunol 14:1030813 |
| abstractText | INTODUCTION: Two scaffold/matrix attachment regions (5'- and 3'-MARs(Emicro) ) flank the intronic core enhancer (cEmicro) within the immunoglobulin heavy chain locus (IgH). Besides their conservation in mice and humans, the physiological role of MARs(Emicro) is still unclear and their involvement in somatic hypermutation (SHM) has never been deeply evaluated. METHODS: Our study analyzed SHM and its transcriptional control in a mouse model devoid of MARs(Emicro) , further combined to relevant models deficient for base excision repair and mismatch repair. RESULTS: We observed an inverted substitution pattern in of MARs(Emicro) -deficient animals: SHM being decreased upstream from cEmicro and increased downstream of it. Strikingly, the SHM defect induced by MARs(Emicro) -deletion was accompanied by an increase of sense transcription of the IgH V region, excluding a direct transcription-coupled effect. Interestingly, by breeding to DNA repair-deficient backgrounds, we showed that the SHM defect, observed upstream from cEmicro in this model, was not due to a decrease in AID deamination but rather the consequence of a defect in base excision repair-associated unfaithful repair process. DISCUSSION: Our study pointed out an unexpected "fence" function of MARs(Emicro) regions in limiting the error-prone repair machinery to the variable region of Ig gene loci. |
