AI Article Synopsis

  • Class switch recombination (CSR) in B cells is crucial for generating diverse antibody isotypes during immune responses, involving specific DNA alterations.
  • Researchers have discovered two isoforms of NME (NME1 and NME2) that affect CSR differently, with NME2 knockdown reducing CSR and NME1 knockdown increasing it.
  • NME1 and NME2 also differ in how they associate with switch (S) regions, with NME1 present before stimulation and NME2 binding only afterwards, highlighting their unique roles in regulating CSR.

Article Abstract

Class switch recombination (CSR) in B cells involves deletion-recombination at switch (S) region DNA and is important for the diversification of antibody isotypes during an immune response. Here, we identify two NME [NM23/NDPK (nucleoside diphosphate kinase)] isoforms, NME1 and NME2, as novel players in this process. Knockdown of NME2 leads to decreased CSR, while knockdown of the highly homologous NME1 results in increased CSR. Interestingly, these NME proteins also display differential occupancy at S regions during CSR despite their homology; NME1 binds to S regions prior to stimulation, while NME2 binds to S regions only after stimulation. To the best of our knowledge, this represents the first report of a role for these proteins in the regulation of CSR.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333498PMC
http://dx.doi.org/10.1002/1873-3468.13290DOI Listing

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