@article {3132733,
	title = {Clonally stable Vkappa allelic choice instructs Igkappa repertoire},
	journal = {Nat Commun},
	volume = {8},
	year = {2017},
	note = {Levin-Klein, RenaFraenkel, ShiraLichtenstein, MichalMatheson, Louise SBartok, OsnatNevo, YuvalKadener, SebastianCorcoran, Anne ECedar, HowardBergman, YehuditengResearch Support, Non-U.S. Gov{\textquoteright}tEnglandNat Commun. 2017 May 30;8:15575. doi: 10.1038/ncomms15575.},
	month = {May 30},
	pages = {15575},
	edition = {2017/05/31},
	abstract = {Although much has been done to understand how rearrangement of the Igkappa locus is regulated during B-cell development, little is known about the way the variable (V) segments themselves are selected. Here we show, using B6/Cast hybrid pre-B-cell clones, that a limited number of V segments on each allele is stochastically activated as characterized by the appearance of non-coding RNA and histone modifications. The activation states are clonally distinct, stable across cell division and developmentally important in directing the Ig repertoire upon differentiation. Using a new approach of allelic ATAC-seq, we demonstrate that the Igkappa V alleles have differential chromatin accessibility, which may serve as the underlying basis of clonal maintenance at this locus, as well as other instances of monoallelic expression throughout the genome. These findings highlight a new level of immune system regulation that optimizes gene diversity.},
	keywords = {*Alleles, Animals, Antibodies/immunology, Chromatin/*metabolism, Female, Genetic Variation, Histones/metabolism, immune system, Immunoglobulin kappa-Chains/*metabolism, Immunoglobulin Variable Region/*genetics, Mice, Mice, Inbred C57BL, Precursor Cells, B-Lymphoid/immunology, RNA, Untranslated/genetics, Transcription, Genetic},
	isbn = {2041-1723 (Electronic)2041-1723 (Linking)},
	author = {Levin-Klein, R. and Fraenkel, S. and Lichtenstein, M. and Matheson, L. S. and Bartok, O. and Nevo, Y. and Kadener, S. and Corcoran, A. E. and Cedar, H. and Bergman, Y.}
}
