BACH2 immunodeficiency illustrates an association between super-enhancers and haploinsufficiency.
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Afzali Behdad, Grönholm Juha, Vandrovcova Jana, O'Brien Charlotte, Sun Hong-Wei, Vanderleyden Ine, Davis Fred P, Khoder Ahmad, Zhang Yu, Hegazy Ahmed N, Villarino Alejandro V, Palmer Ira W, Kaufman Joshua, Watts Norman R, Kazemian Majid, Kamenyeva Olena, Keith Julia, Sayed Anwar, Kasperaviciute Dalia, Mueller Michael, Hughes Jason D, Fuss Ivan J, Sadiyah Mohammed F, Montgomery-Recht Kim, McElwee Joshua, Restifo Nicholas P, Strober Warren, Linterman Michelle A, Wingfield Paul T, Uhlig Holm H, Roychoudhuri Rahul, Aitman Timothy J, Kelleher Peter, Lenardo Michael J, O'Shea John J, Cooper Nichola, Laurence Arian D J
Аннотация
The transcriptional programs that guide lymphocyte differentiation depend on the precise expression and timing of transcription factors (TFs). The TF BACH2 is essential for T and B lymphocytes and is associated with an archetypal super-enhancer (SE). Single-nucleotide variants in the BACH2 locus are associated with several autoimmune diseases, but BACH2 mutations that cause Mendelian monogenic primary immunodeficiency have not previously been identified. Here we describe a syndrome of BACH2-related immunodeficiency and autoimmunity (BRIDA) that results from BACH2 haploinsufficiency. Affected subjects had lymphocyte-maturation defects that caused immunoglobulin deficiency and intestinal inflammation. The mutations disrupted protein stability by interfering with homodimerization or by causing aggregation. We observed analogous lymphocyte defects in Bach2-heterozygous mice. More generally, we observed that genes that cause monogenic haploinsufficient diseases were substantially enriched for TFs and SE architecture. These findings reveal a previously unrecognized feature of SE architecture in Mendelian diseases of immunity: heterozygous mutations in SE-regulated genes identified by whole-exome/genome sequencing may have greater significance than previously recognized.