All known in vivo functions of the Oct-2 transcription factor require the C-terminal protein domain

被引:17
作者
Corcoran, LM
Koentgen, F
Dietrich, W
Veale, M
Humbert, PO
机构
[1] Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
[2] Ozgene, Nedlands, WA, Australia
[3] Peter MacCallum Canc Inst, Melbourne, Vic, Australia
关键词
D O I
10.4049/jimmunol.172.5.2962
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Oct-2, a transcription factor expressed in the B lymphocyte lineage and in the developing CNS, functions through of a number of discrete protein domains. These include a DNA-binding POU homeodomain flanked by two transcriptional activation domains. In vitro studies have shown that the C-terminal activation domain, a serine-, threonine- and proline-rich sequence, possesses unique qualities, including the ability to activate transcription from a distance in a B cell-specific manner. In this study, we describe mice in which the endogenous oct-2 gene has been modified through gene targeting to create a mutated allele, oct-2DeltaC, which encodes Oct-2 protein isoforms that lack all sequence C-terminal to the DNA-binding domain. Surprisingly, despite the retention of the DNA-binding domain and the glutamine-rich N-terminal activation domain, the truncated protein(s) encoded by the oct-2DeltaC allele are unable to rescue any of the previously described defects exhibited by oct-2 null mice. Homozygous oct-2DeltaC/DeltaC mice die shortly after birth, and B cell maturation, B-1 cell self renewal, serum Ig levels, and B lymphocyte responses to in vitro stimulation are all reduced or absent, to a degree equivalent to that seen in oct-2 null mice. We conclude that the C-terminal activation domain of Oct-2 is required to mediate the unique and indispensable functions of the Oct-2 transcription factor in vivo.
引用
收藏
页码:2962 / 2969
页数:8
相关论文
共 58 条
[1]   High mobility group I/Y protein functions as a specific cofactor for Oct-2A: mapping of interaction domains [J].
Abdulkadir, SA ;
Casolaro, V ;
Tai, AKF ;
Thanos, D ;
Ono, SJ .
JOURNAL OF LEUKOCYTE BIOLOGY, 1998, 64 (05) :681-691
[2]  
ALLMAN DM, 1992, J IMMUNOL, V149, P2533
[3]  
ALLMAN DM, 1993, J IMMUNOL, V151, P4431
[4]   FUNCTIONAL DIFFERENCES BETWEEN THE OCT2 TRANSACTIVATION DOMAINS DETERMINE THE TRANSACTIVATION POTENTIAL OF INDIVIDUAL OCT2 ISOFORMS [J].
ANNWEILER, A ;
ZWILLING, S ;
WIRTH, T .
NUCLEIC ACIDS RESEARCH, 1994, 22 (20) :4250-4258
[5]   OCT-2 FACILITATES FUNCTIONAL PREINITIATION COMPLEX ASSEMBLY AND IS CONTINUOUSLY REQUIRED AT THE PROMOTER FOR MULTIPLE ROUNDS OF TRANSCRIPTION [J].
ARNOSTI, DN ;
MERINO, A ;
REINBERG, D ;
SCHAFFNER, W .
EMBO JOURNAL, 1993, 12 (01) :157-166
[6]   Transcription factor NF-kappa B regulates inducible Oct-2 gene expression in precursor B lymphocytes [J].
Bendall, HH ;
Scherer, DC ;
Edson, CR ;
Ballard, DW ;
Oltz, EM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (46) :28826-28828
[7]   POU/TBP cooperativity: A mechanism for enhancer action from a distance [J].
Bertolino, E ;
Singh, H .
MOLECULAR CELL, 2002, 10 (02) :397-407
[8]   TRANSITIONAL B-CELLS ARE THE TARGET OF NEGATIVE SELECTION IN THE B-CELL COMPARTMENT [J].
CARSETTI, R ;
KOHLER, G ;
LAMERS, MC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (06) :2129-2140
[9]   THE B-CELL-SPECIFIC OCT-2 PROTEIN CONTAINS POU BOX-TYPE AND HOMEO BOX-TYPE DOMAINS [J].
CLERC, RG ;
CORCORAN, LM ;
LEBOWITZ, JH ;
BALTIMORE, D ;
SHARP, PA .
GENES & DEVELOPMENT, 1988, 2 (12A) :1570-1581
[10]   OCTAMER-BINDING PROTEINS IN DIVERSE HEMATOPOIETIC-CELLS [J].
COCKERILL, PN ;
KLINKEN, SP .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (03) :1293-1296