Abstract

To isolate new zinc finger genes expressed at early stages of peripheral nerve development, we have used PCR to amplify conserved zinc finger sequences. RNA from rat embryonic day 12 and 13 sciatic nerves, a stage when nerves contain Schwann cell precursors, was used to identify several genes not previously described in Schwann cells. One of them, zinc finger protein (ZFP)-57, proved to be the homologue of a mouse gene found in F9 teratocarcinoma cells. Its mRNA expression profile within embryonic and adult normal and transected peripheral nerves, and its distribution in the rest of the nervous system is described. High levels of expression are seen in embryonic nerves and spinal cord. These drop rapidly during the first few weeks after birth, a pattern mirrored in other parts of the nervous system. ZFP-57 localizes to the nucleus of Schwann and other cells. The sequence contains an N-terminal Krüppel-associated box (KRAB) domain and ZFP-57 constructs containing green fluorescent protein reveal that the protein colocalizes with heterochromatin protein 1alpha to centromeric heterochromatin in a characteristic speckled pattern in NIH3T3 cells. The KRAB domain is required for this localization, because constructs lacking it target the protein to the nucleus but not to the centromeric heterochromatin. When fused to a heterologous DNA binding domain, the KRAB domain of ZFP-57 represses transcription, and full-length ZFP-57 represses Schwann cell transcription from myelin basic protein and P(0) promoters in co-transfection assays. Zfp-57 mRNA is up-regulated in Schwann cells in response to leukemia inhibitory factor and fibroblast growth factor 2.

Highlights

  • To isolate new zinc finger genes expressed at early stages of peripheral nerve development, we have used PCR to amplify conserved zinc finger sequences

  • We have isolated the rat Zfp-57 gene using a fast and simple approach to search for novel zinc finger transcription factors expressed during embryonic development of the peripheral nervous system

  • The modular structure of the C2H2 zinc finger motif found in tandem orientation in many transcription factors enabled us to use a modification of a PCR-based genetic screen described previously by Pellegrino and Berg [65]

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Summary

The abbreviations used are

E, embryo day; Zfp, zinc finger protein; KRAB, Kruppel-associated box; DBD, DNA binding domain; HP1, heterochromatin protein 1; LIF, leukemia inhibitory factor; GFP, green fluorescent protein; CAT, chloramphenicol acetyltransferase; ER, estrogen receptor; MBP, myelin basic protein; PGK, phosphoglycerate kinase; DMEM, Dulbecco’s modified Eagle’s medium; FCS, fetal calf serum; FGF-2, fibroblast growth factor 2; P, postnatal day; JAK, Janusactivated kinase; STAT, stress-activated kinase; p75NTR, p75 neurotrophin receptor; DRG, dorsal root ganglia; EGFP, enhanced green fluorescent protein; DAPI, 4Ј,6-diamidino-2-phenylindole; RT, reverse transcriptase; tk, thymidine kinase; IPTG, isopropyl-1-thio-␤D-galactopyranoside; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; BrdUrd, bromodeoxyuridine. Five of which have been shown to be transcription factors, have previously been identified in Schwann cells [13, 19, 22,23,24,25]. The Egr family, comprises only a small proportion of the total number of known zinc finger transcription factors, more than 700 of which have been identified. The properties and distribution of one of these, Zfp-57, is described below This gene, which contains a KRAB domain, shows strong developmental regulation both in the peripheral and central nervous systems, localizes to heterochromatin in cell nuclei and represses activation of myelin promoter and reporter constructs in co-transfection assays

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