In recent years, major developments have been made in
understanding various genetic and epigenetic regulatory processes
that are critical for the generation of B cell repertoires. These
include the role of chromatin regulation and nuclear organization
in understating the IgH gene regulation. A role and mechanism of
DNA repair proteins in somatic hypermutation has been elucidated.
Genetic mutation studies have been instrumental in providing
insight into some of the mechanisms involved in targeting CSR to
various switch DNA regions located upstream of C region genes,
especially a role of AID motifs, transcription, and R-loops. Recent
studies support a dominant role of receptor editing in central B
cell tolerance and signaling pathways that regulate receptor
editing in self-reactive and non-self-reactive immature B cells.
These were some of the topics of discussion at the 11th
International Conference on B cell Biology. These proceedings
highlight recent developments in lymphocyte development, Ig gene
rearrangements and somatic hypermutation, chromatin structure
modification, B lymphocyte signaling and fate, receptor editing,
and autoimmunity.
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