DEVELOPMENTAL EXPRESSION OF THE TRANSCRIPTION FACTOR ZIF268 IN RAT-BRAIN

被引:37
作者
HERMS, J
ZURMOHLE, U
SCHLINGENSIEPEN, R
BRYSCH, W
SCHLINGENSIEPEN, KH
机构
[1] MAX PLANCK INST BIOPHYS CHEM,NEUROBIOL ABT,D-37077 GOTTINGEN,GERMANY
[2] UNIV HOSP GOTTINGEN,DEPT PAEDIAT & CHILD NEUROL,GOTTINGEN,GERMANY
关键词
ZIF268; MESSENGER-RNA EXPRESSION; DEVELOPMENT; IN SITU HYBRIDIZATION; RAT BRAIN;
D O I
10.1016/0304-3940(94)90737-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Changes in the distribution pattern of mRNA encoding the zif268 transcription factor (also referred to as NGFI-A, Krox-24 or EGR-1) were investigated by in situ hybridization histochemistry during postnatal rat brain development. Marked changes in zif268 expression patterns were seen in particular in the cerebral cortex and the hippocampal formation during the first 3 wk. In the Ist postnatal week, zif268 mRNA levels were highest in the corpus striatum and the piriform cortex. In the neocortex, expression rose sharply in the sensorymotor area between postnatal days (PNDs) 10 and 12. In the frontal and occipital cortex, in contrast, an increase in zif268 mRNA levels was first seen on PND 14. After PND 17, levels decreased in the sensorymotor and the frontal cortex but remained high in the occipital and the piriform cortex. In the hippocampus, an initially uniform increase in expression during the 2nd week was followed by a marked dissociation in expression levels between CA1, with continuously high expression levels on the one hand, and CA3, CA4 and the dentate gyrus, with a strong decline of expression during the 3rd week, on the other hand. Our results indicate that zif268 expression displays a highly dynamic expression pattern during plastic adaptations of different cerebral subregions during postnatal development, suggesting a possible involvement in gene regulatory processes during these phases.
引用
收藏
页码:171 / 174
页数:4
相关论文
共 26 条
[11]   LONG-TERM POTENTIATION OF GUINEA-PIG MOSSY FIBER RESPONSES IS NOT BLOCKED BY N-METHYL D-ASPARTATE ANTAGONISTS [J].
HARRIS, EW ;
COTMAN, CW .
NEUROSCIENCE LETTERS, 1986, 70 (01) :132-137
[12]   DEVELOPMENTAL ONSET OF LONG-TERM POTENTIATION IN AREA CA1 OF THE RAT HIPPOCAMPUS [J].
HARRIS, KM ;
TEYLER, TJ .
JOURNAL OF PHYSIOLOGY-LONDON, 1984, 346 (JAN) :27-&
[13]   THE KROX-24 PROTEIN, A NEW TRANSCRIPTION REGULATING FACTOR - EXPRESSION IN THE RAT CENTRAL-NERVOUS-SYSTEM FOLLOWING AFFERENT SOMATOSENSORY STIMULATION [J].
HERDEGEN, T ;
WALKER, T ;
LEAH, JD ;
BRAVO, R ;
ZIMMERMANN, M .
NEUROSCIENCE LETTERS, 1990, 120 (01) :21-24
[14]  
JACOBSON M, 1991, DEV NEUROBIOL, P95
[15]   2 MOUSE GENES ENCODING POTENTIAL TRANSCRIPTION FACTORS WITH IDENTICAL DNA-BINDING DOMAINS ARE ACTIVATED BY GROWTH-FACTORS IN CULTURED-CELLS [J].
LEMAIRE, P ;
REVELANT, O ;
BRAVO, R ;
CHARNAY, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (13) :4691-4695
[16]   INDUCTION OF TRANSCRIPTION FACTORS IN SOMATOSENSORY CORTEX AFTER TACTILE STIMULATION [J].
MACK, KJ ;
MACK, PA .
MOLECULAR BRAIN RESEARCH, 1992, 12 (1-3) :141-147
[17]   QUANTITATIVE ASSESSMENT OF NEUROPROTECTION AGAINST NMDA-INDUCED BRAIN INJURY [J].
MCDONALD, JW ;
ROESER, NF ;
SILVERSTEIN, FS ;
JOHNSTON, MV .
EXPERIMENTAL NEUROLOGY, 1989, 106 (03) :289-296
[18]   A NERVE GROWTH-FACTOR INDUCED GENE ENCODES A POSSIBLE TRANSCRIPTIONAL REGULATORY FACTOR [J].
MILBRANDT, J .
SCIENCE, 1987, 238 (4828) :797-799
[19]   THE CURRENT EXCITEMENT IN LONG-TERM POTENTIATION [J].
NICOLL, RA ;
KAUER, JA ;
MALENKA, RC .
NEURON, 1988, 1 (02) :97-103
[20]   POSTNATAL DEVELOPMENTAL PROFILES OF FILAMENTOUS ACTIN AND OF 200 KDA NEUROFILAMENT POLYPEPTIDE IN THE VISUAL-CORTEX OF LIGHT-REARED AND DARK-REARED RATS AND THEIR RELATIONSHIP TO CRITICAL PERIOD PLASTICITY [J].
NONA, SN ;
TROWELL, SC ;
CRONLYDILLON, JR .
FEBS LETTERS, 1985, 186 (01) :111-115