A NOVEL POU FAMILY TRANSCRIPTION FACTOR IS CLOSELY RELATED TO BRN-3 BUT HAS A DISTINCT EXPRESSION PATTERN IN NEURONAL CELLS

被引:117
作者
LILLYCROP, KA
BUDRAHAN, VS
LAKIN, ND
TERRENGHI, G
WOOD, JN
POLAK, JM
LATCHMAN, DS
机构
[1] UNIV COLL & MIDDLESEX SCH MED, DEPT BIOCHEM,MED MOLEC BIOL UNIT,WINDEYER BLDG, CLEVELAND ST, LONDON W1P 6DB, ENGLAND
[2] UNIV COLL & MIDDLESEX SCH MED, DEPT CHEM PATHOL, DIV MOLEC PATHOL, LONDON W1P 6DB, ENGLAND
[3] HAMMERSMITH HOSP, ROYAL POSTGRAD MED SCH, DEPT HISTOCHEM, LONDON W12 0HS, ENGLAND
[4] SANDOZ, INST MED RES, LONDON WC1E 6BW, ENGLAND
基金
英国医学研究理事会;
关键词
D O I
10.1093/nar/20.19.5093
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The use of the polymerase chain reaction in conjunction with degenerate oligonucleotides has allowed the isolation of cDNA clones derived from each of the POU family transcription factors expressed in the proliferating ND7 neuronal cell line. In addition to the previously characterized Oct-1, Oct-2 and Brn-3 factors, ND7 cells have been shown by this means to express a novel POU factor. This factor is closely related to Brn-3 but differs at seven amino acids in the POU domain, one of which is located in a region which is critical for protein-protein interactions between different POU proteins. Like Brn-3, the novel factor is expressed at high levels in embryonic brain and declines in abundance during neuronal development. In contrast to Brn-3 however, it is absent in mature sensory neurons and its expression declines during the in vitro differentiation of ND7 cells to a non-dividing phenotype whilst Brn-3 expression increases. The significance of these distinct but overlapping expression patterns is discussed in terms of the possible role of these two factors in regulating neuronal gene expression.
引用
收藏
页码:5093 / 5096
页数:4
相关论文
共 33 条
[1]   ESTABLISHMENT OF FUNCTIONAL CLONAL LINES OF NEURONS FROM MOUSE NEUROBLASTOMA [J].
AUGUSTIT.G ;
SATO, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1969, 64 (01) :311-&
[2]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[3]   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
[4]   A GENETIC PATHWAY FOR THE DEVELOPMENT OF THE CAENORHABDITIS-ELEGANS HSN MOTOR NEURONS [J].
DESAI, C ;
GARRIGA, G ;
MCINTIRE, SL ;
HORVITZ, HR .
NATURE, 1988, 336 (6200) :638-646
[5]   THE C-ELEGANS CELL LINEAGE AND DIFFERENTIATION GENE UNC-86 ENCODES A PROTEIN WITH A HOMEODOMAIN AND EXTENDED SIMILARITY TO TRANSCRIPTION FACTORS [J].
FINNEY, M ;
RUVKUN, G ;
HORVITZ, HR .
CELL, 1988, 55 (05) :757-769
[6]   PURIFICATION AND CHARACTERIZATION OF OTF-1, A TRANSCRIPTION FACTOR REGULATING CELL-CYCLE EXPRESSION OF A HUMAN HISTONE H2B GENE [J].
FLETCHER, C ;
HEINTZ, N ;
ROEDER, RG .
CELL, 1987, 51 (05) :773-781
[7]   HOMEO BOXES IN THE STUDY OF DEVELOPMENT [J].
GEHRING, WJ .
SCIENCE, 1987, 236 (4806) :1245-1252
[8]   CLONING AND SEQUENCING OF POU-BOXES EXPRESSED IN MOUSE TESTIS [J].
GOLDSBOROUGH, A ;
ASHWORTH, A ;
WILLISON, K .
NUCLEIC ACIDS RESEARCH, 1990, 18 (06) :1634-1634
[9]   HUMAN BETA-GLOBIN PRE-MRNA SYNTHESIZED INVITRO IS ACCURATELY SPLICED IN XENOPUS OOCYTE NUCLEI [J].
GREEN, MR ;
MANIATIS, T ;
MELTON, DA .
CELL, 1983, 32 (03) :681-694
[10]   ESTABLISHMENT OF A NORADRENERGIC CLONAL LINE OF RAT ADRENAL PHEOCHROMOCYTOMA CELLS WHICH RESPOND TO NERVE GROWTH-FACTOR [J].
GREENE, LA ;
TISCHLER, AS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (07) :2424-2428