Localization of the human HF.10 finger gene on a chromosome region (3p21?22) frequently deleted in human cancers
- 1 April 1990
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 84 (5) , 391-395
- https://doi.org/10.1007/bf00195806
Abstract
The finger motif is a tandemly repeated DNA-binding domain recently identified in the primary structure of several eukaryotic transcriptional regulatory proteins. It has been proposed that some members of the finger-gene family are implicated in both normal cell proliferation and differentiation. We isolated several human finger genes by means of hybridization with a finger motif-containing DNA probe. One of these finger genes, HF.10, is expressed at low levels in a variety of human tissues and is down-regulated during the in vitro terminal differentiation of human leukemic myeloid cell lines. By in situ hybridization experiments and analysis of interspecific somatic cell hybrids we mapped the HF.10 gene to 3p21–22, a chromosome region frequently involved in karyotypic rearrangements associated with lung and renal cancer.Keywords
This publication has 48 references indexed in Scilit:
- Detection of specific sequences among DNA fragments separated by gel electrophoresisPublished by Elsevier ,2006
- Retroviral activation of a novel gene encoding a zinc finger protein in IL-3-dependent myeloid leukemia cell linesCell, 1988
- Molecular analysis of a t(7;14)(g35;g32) chromosome translocation in a T cell leukemia of a patient with ataxia telangiectasiaCell, 1988
- Molecular Analysis of the Short Arm of Chromosome 3 in Small-Cell and Non-Small-Cell Carcinoma of the LungNew England Journal of Medicine, 1987
- Deletion 3p in two lung adenocarcinomas metastatic to the brainCancer Genetics and Cytogenetics, 1987
- The primary structure of transcription factor TFIIIA has 12 consecutive repeatsFEBS Letters, 1985
- A 3p deletion in small cell lung carcinomaCancer Genetics and Cytogenetics, 1985
- Production of phenocopies by Krüppel antisense RNA injection into Drosophila embryosNature, 1985
- Recurrent chromosomal defects are found in most patients with non-Hodgkin's-lymphomaCancer Genetics and Cytogenetics, 1984
- New chromosomal translocations correlate with specific immunophenotypes of childhood acute lymphoblastic leukemiaCell, 1984