TY - JOUR

T1 - Amplification of the E2F1 transcription factor gene in the HEL erythroleukemia cell line.

AU - Saito, M

AU - Helin, K

AU - Valentine, M B

AU - Griffith, B B

AU - Willman, C L

AU - Harlow, E

AU - Look, A T

N1 - Keywords: Animals; Base Sequence; Blotting, Northern; Blotting, Southern; Carrier Proteins; Cell Cycle Proteins; Cell Division; Cell Line; Chromosome Mapping; Chromosomes, Human, Pair 20; Cloning, Molecular; Cricetinae; DNA-Binding Proteins; E2F Transcription Factors; E2F1 Transcription Factor; E2F2 Transcription Factor; E2F3 Transcription Factor; Gene Amplification; Gene Expression; Genes, Tumor Suppressor; Hematopoietic Stem Cells; Humans; Hybrid Cells; In Situ Hybridization, Fluorescence; Leukemia, Erythroblastic, Acute; Molecular Sequence Data; Multigene Family; Myelodysplastic Syndromes; RNA, Messenger; Telomere; Transcription Factor DP1; Transcription Factors; Tumor Cells, Cultured

PY - 1995

Y1 - 1995

N2 - The E2F transcription factor plays an important regulatory role in cell proliferation, mediating the expression of genes whose products are essential for inducing resting cells to enter the cell cycle and synthesize DNA. To investigate the possible involvement of E2F in hematopoietic malignancies, we isolated genomic clones encompassing the human E2F1 gene. We then used fluorescence in situ hybridization to localize E2F1 to human chromosome 20q11, telomeric to the p107 locus, a gene whose product is related to the retinoblastoma gene product (pRb). This finding contrasts with the 1p36 and 6q22 chromosomal locations previously assigned E2F2 and E2F3, two additional members of the E2F family. Although deletions or structural rearrangements of E2F1 were not detected in 14 primary acute leukemia or myelodysplasia samples with structural abnormalities of chromosome 20q11, the gene was amplified and overexpressed in HEL erythroleukemia cells and translocated to other chromosomes in several established human leukemia cell lines. This study provides the first evidence of gene amplification involving a member of the E2F family of transcription factors. We propose that E2F1 overexpression in erythroid progenitors may stimulate abnormal cell proliferation by overriding negative regulatory signals mediated by tumor suppressor proteins such as pRb.

AB - The E2F transcription factor plays an important regulatory role in cell proliferation, mediating the expression of genes whose products are essential for inducing resting cells to enter the cell cycle and synthesize DNA. To investigate the possible involvement of E2F in hematopoietic malignancies, we isolated genomic clones encompassing the human E2F1 gene. We then used fluorescence in situ hybridization to localize E2F1 to human chromosome 20q11, telomeric to the p107 locus, a gene whose product is related to the retinoblastoma gene product (pRb). This finding contrasts with the 1p36 and 6q22 chromosomal locations previously assigned E2F2 and E2F3, two additional members of the E2F family. Although deletions or structural rearrangements of E2F1 were not detected in 14 primary acute leukemia or myelodysplasia samples with structural abnormalities of chromosome 20q11, the gene was amplified and overexpressed in HEL erythroleukemia cells and translocated to other chromosomes in several established human leukemia cell lines. This study provides the first evidence of gene amplification involving a member of the E2F family of transcription factors. We propose that E2F1 overexpression in erythroid progenitors may stimulate abnormal cell proliferation by overriding negative regulatory signals mediated by tumor suppressor proteins such as pRb.

M3 - Journal article

C2 - 7774910

VL - 25

SP - 130

EP - 138

JO - Genomics

JF - Genomics

SN - 0888-7543

IS - 1

ER -