Many levels of control of V gene rearrangement frequency

被引:26
作者
Feeney, AJ [1 ]
Goebel, P [1 ]
Espinoza, CR [1 ]
机构
[1] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
关键词
D O I
10.1111/j.0105-2896.2004.00163.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
V, D, and J gene segments rearrange at very different frequencies. As with most biological systems, there are multiple levels of control of V gene recombination frequency, and here we review some of the work from our laboratory that addresses these various control mechanisms. One of the important factors that affect non-random V gene rearrangement frequency is the natural heterogeneity in recombination signal sequences (RSSs). Not only does variation in the heptamer and nonamer affect rearrangement, but variation in the spacer can also dramatically affect recombination. However, there are clearly other factors which control V gene rearrangement, as revealed by the fact that genes with identical RSSs can rearrange at different frequencies in vivo. Some of these other influences most likely affect the earliest stages of control - the change from an inaccessible state to an accessible state. Transcription factors can play a role in inducing these changes. Rearrangement of many VkappaI genes can be induced in a non-lymphoid cell line after ectopic expression of E2A, while neighboring VkappaII and VkappaIII genes do not rearrange, demonstrating that at least one level of control of induction of accessibility occurs at the level of the individual gene. Also, changes in chromatin structure can affect accessibility and might influence individual V gene rearrangement frequency.
引用
收藏
页码:44 / 56
页数:13
相关论文
共 79 条
[11]   Regulation of E2A activities by histone acetyltransferases in B lymphocyte development [J].
Bradney, C ;
Hjelmeland, M ;
Komatsu, Y ;
Yoshida, M ;
Yao, TP ;
Zhuang, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (04) :2370-2376
[12]  
BREZINSCHEK HP, 1995, J IMMUNOL, V155, P190
[13]   ANTI-PHOSPHORYLCHOLINE ANTIBODIES OF THE T15 IDIOTYPE ARE OPTIMALLY PROTECTIVE AGAINST STREPTOCOCCUS-PNEUMONIAE [J].
BRILES, DE ;
FORMAN, C ;
HUDAK, S ;
CLAFLIN, JL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1982, 156 (04) :1177-1185
[15]   A three-megabase yeast artificial chromosome Contig spanning the C57BL mouse Igh locus [J].
Chevillard, C ;
Ozaki, J ;
Herring, CD ;
Riblet, R .
JOURNAL OF IMMUNOLOGY, 2002, 168 (11) :5659-5666
[16]   Transient IL-7/IL-7R signaling provides a mechanism for feedback inhibition of immunoglobulin heavy chain gene rearrangements [J].
Chowdhury, D ;
Sen, R .
IMMUNITY, 2003, 18 (02) :229-241
[17]   Stepwise activation of the immunoglobulin μ heavy chain gene locus [J].
Chowdhury, D ;
Sen, R .
EMBO JOURNAL, 2001, 20 (22) :6394-6403
[18]   UNIFORMITY IN CLONAL REPERTOIRE FOR IMMUNE-RESPONSE TO PHOSPHORYLCHOLINE IN MICE [J].
CLAFLIN, JL .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1976, 6 (10) :669-674
[19]  
CONNOR AM, 1995, J IMMUNOL, V155, P5268
[20]   Impaired immunoglobulin gene rearrangement in mice lacking the IL-7 receptor [J].
Corcoran, AE ;
Riddell, A ;
Krooshoop, D ;
Venkitaraman, AR .
NATURE, 1998, 391 (6670) :904-907