A NOVEL BRN3-LIKE POU TRANSCRIPTION FACTOR EXPRESSED IN SUBSETS OF RAT SENSORY AND SPINAL-CORD NEURONS

被引:107
作者
NINKINA, NN
STEVENS, GEM
WOOD, JN
RICHARDSON, WD
机构
[1] SANDOZ INST MED RES, 5 GOWER PL, LONDON WC1E 6BN, ENGLAND
[2] UNIV LONDON UNIV COLL, DEPT BIOL, LONDON WC1E 6BT, ENGLAND
[3] ENGELHARDT INST MOLEC BIOL, MOSCOW, RUSSIA
关键词
D O I
10.1093/nar/21.14.3175
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
Brn3a and Brn3b are mammalian members of the POU class of transcription factors. They are closely related to each other and to Unc86, which determines the normal development of certain cells, including mechanoreceptive sensory neurons in Caenorhabditis elegans. We screened a rat dorsal root ganglion (DRG) cDNA library at moderate stringency with a Brn3a POU-domain probe and identified a novel transcript encoding a POU protein that we have named Brn3c. Brn3c closely resembles Brn3a and Brn3b in its POU-domain and thus helps define a family of Unc86-related mammalian POU factors. Both Brn3a and Brn3c are expressed only in the central and peripheral nervous systems. In the neonatal rat, northern blots revealed a 3.6 kb Brn3a transcript in DRG, spinal cord and hindbrain, and a 2.6 kb Brn3c transcript in DRG and spinal cord. In situ hybridization showed that most DRG neurons express Brn3a whereas only a small subset of neurons expresses Brn3c. In the spinal cord, Brn3a is expressed by many dorsal horn neurons. In contrast, Brn3c is expressed by a very small number of cells in laminae 4/5 of the dorsal horn. These data suggest that Brn3-related POU factors may be involved in the development or function of particular subclasses of sensory and spinal cord neurons.
引用
收藏
页码:3175 / 3182
页数:8
相关论文
共 28 条
[1]   GENERAL METHOD FOR ISOLATION OF HIGH MOLECULAR-WEIGHT DNA FROM EUKARYOTES [J].
BLIN, N ;
STAFFORD, DW .
NUCLEIC ACIDS RESEARCH, 1976, 3 (09) :2303-2308
[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]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[4]   A NOVEL POU HOMEODOMAIN GENE SPECIFICALLY EXPRESSED IN CELLS OF THE DEVELOPING MAMMALIAN NERVOUS-SYSTEM [J].
COLLUM, RG ;
FISHER, PE ;
DATTA, M ;
MELLIS, S ;
THIELE, C ;
HUEBNER, K ;
CROCE, CM ;
ISRAEL, MA ;
THEIL, T ;
MOROY, T ;
DEPINHO, R ;
ALT, FW .
NUCLEIC ACIDS RESEARCH, 1992, 20 (18) :4919-4925
[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]  
GERRERO MR, 1993, J CELL BIOCHEM, P158
[7]   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
[8]   MECHANISMS OF COMPLEX TRANSCRIPTIONAL REGULATION - IMPLICATIONS FOR BRAIN-DEVELOPMENT [J].
HE, X ;
ROSENFELD, MG .
NEURON, 1991, 7 (02) :183-196
[9]   THE POU DOMAIN - A LARGE CONSERVED REGION IN THE MAMMALIAN PIT-1, OCT-1, OCT-2, AND CAENORHABDITIS-ELEGANS UNC-86 GENE-PRODUCTS [J].
HERR, W ;
STURM, RA ;
CLERC, RG ;
CORCORAN, LM ;
BALTIMORE, D ;
SHARP, PA ;
INGRAHAM, HA ;
ROSENFELD, MG ;
FINNEY, M ;
RUVKUN, G ;
HORVITZ, HR .
GENES & DEVELOPMENT, 1988, 2 (12A) :1513-1516
[10]   A SINGLE AMINO-ACID EXCHANGE TRANSFERS VP16-INDUCED POSITIVE CONTROL FROM THE OCT-1 TO THE OCT-2 HOMEO DOMAIN [J].
LAI, JS ;
CLEARY, MA ;
HERR, W .
GENES & DEVELOPMENT, 1992, 6 (11) :2058-2065