NEURAL-SPECIFIC EXPRESSION, GENOMIC STRUCTURE, AND CHROMOSOMAL LOCALIZATION OF THE GENE ENCODING THE ZINC-FINGER TRANSCRIPTION FACTOR NGFI-C

被引:65
作者
CROSBY, SD
VEILE, RA
DONISKELLER, H
BARABAN, JM
BHAT, RV
SIMBURGER, KS
MILBRANDT, J
机构
[1] WASHINGTON UNIV, SCH MED,DEPT PATHOL,DIV LAB MED,BOX 8118, 660 S EUCLID AVE, ST LOUIS, MO 63110 USA
[2] WASHINGTON UNIV, SCH MED, DEPT INTERNAL MED, ST LOUIS, MO 63110 USA
[3] WASHINGTON UNIV, SCH MED, DEPT GENET, ST LOUIS, MO 63110 USA
[4] JOHNS HOPKINS UNIV, SCH MED, DEPT NEUROSCI, BALTIMORE, MD 21205 USA
关键词
D O I
10.1073/pnas.89.10.4739
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The nerve growth factor-induced clone C (NGFI-C) gene encodes a zinc-finger transcription factor that is rapidly induced by nerve growth factor in rat pheochromocytoma PC12 cells and by seizure in brain. NGFI-C is closely related to the previously described early response genes, nerve growth factor-induced clone A (NGFI-A or EGR1), EGR2, and EGR3. These four early response (immediate early) proteins all contain very similar zinc-finger DNA binding domains; in addition, analysis of the non-zinc-ringer region revealed that they share an additional five highly homologous subdomains, four of which are within the amino terminus. The 5' flanking region of NGFI-C contains several cAMP response elements but does not contain any serum-response elements or CArG boxes [CC(A/T)6GG], cis-acting elements commonly involved in early response gene regulation. NGFI-C mRNA was detected in neural tissues of postnatal animals, but no expression was found in rat embryos. In situ hybridization demonstrated that NGFI-C is rapidly induced in the dentate gyrus of the hippocampus after seizure, but in contrast to NGFI-A, increases in NGFI-C mRNA were not detected in the overlying cortex. By using fluorescence in situ hybridization, NGFI-C was localized to human chromosome 2p13. This region contains a constitutive fragile site that is associated with chromosomal breakpoints and translocations characteristic of some chronic lymphocytic leukemias.
引用
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页码:4739 / 4743
页数:5
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