BACH2 immunodeficiency illustrates an association between super-enhancers and haploinsufficiency

Behdad Afzali, Juha Grönholm, Jana Vandrovcova, Charlotte O'Brien, Hong Wei Sun, Ine Vanderleyden, Fred P. Davis, Ahmad Khoder, Yu Zhang, Ahmed N. Hegazy, Alejandro V. Villarino, Ira W. Palmer, Joshua Kaufman, Norman R. Watts, Majid Kazemian, Olena Kamenyeva, Julia Keith, Anwar Sayed, Dalia Kasperaviciute, Michael MuellerJason D. Hughes, Ivan J. Fuss, Mohammed F. Sadiyah, Kim Montgomery-Recht, Joshua McElwee, Nicholas P. Restifo, Warren Strober, Michelle A. Linterman, Paul T. Wingfield, Holm H. Uhlig, Rahul Roychoudhuri, Timothy J. Aitman, Peter Kelleher, Michael J. Lenardo, John J. O'Shea, Nichola Cooper, Arian D.J. Laurence

Research output: Contribution to journalArticlepeer-review

70 Scopus citations

Abstract

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.

Original languageEnglish (US)
Pages (from-to)813-823
Number of pages11
JournalNature Immunology
Volume18
Issue number7
DOIs
StatePublished - Jun 20 2017
Externally publishedYes

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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