Molecular characterization and chromosomal localization of DRT (EPHT3): A developmentally regulated human protein - tyrosine kinase gene of the EPH family

Naohiko Ikegaki, Xao X. Tang, Xing Ge Liu, Jaclyn A. Biegel, Cindy Allen, Akira Yoshioka, Erik P. Sulman, Garrett M. Brodeur, David E Pleasure

Research output: Contribution to journalArticle

29 Citations (Scopus)

Abstract

By screening a human fetal brain cDNA expression library using a monocional antiphosphotyrosine antibody and by 5' RACE procedures, we have isolated overlapping cDNAs encoding a receptor-type tyrosine kinase belonging to the EPH family, DRT (Developmentally Regulated EPH-related Tyrosine kinase gene). The DRT gene is expressed in three different size transcripts (i.e. 4, 5 and 11 kb). DRT transcripts are expressed in human brain and several other tissues, including heart, lung, kidney, placenta, pancreas, liver and skeletal muscle, but the 11 kb DRT transcript is preferentially expressed in fetal brain. Steady-state levels of DRT mRNA in several tissues, including brain, heart, lung and kidney, are greater in the midterm fetus than those in the adult. DRT transcripts are detectable at low levels in a human teratocarcinoma cell line (NTera-2), but its expression is greatly increased after the NTera-2 cells are induced to become postmitotic neurons (NTera-2N) by retinoic acid treatment. These data suggest that DRT plays a part in human neurogenesis. A large number of tumor cell lines derived from neuroectoderm express DRT transcripts, including 12 neuroblastomas, two medulloblastomas, one primitive neuroectodermal tumor and six small cell lung carcinomas (SCLC). Interestingly, several neuroblastoma cell lines with 1p deletion and one SCLC cell line express DRT transcripts of aberrant size (i.e. 3, 6 and 8 kb) in addition to those found in normal tissues. We mapped the DRT gene to human chromosome 1p35-1p36.1 by PCR screening of human-rodent somatic cell hybrid panels and by fluorescence in situ hybridization. As the distal end of chromosome 1p is often deleted in neuroblastomas and altered in some cases in SCLCs, these chromosomal abnormalities may have resulted in the generation of aberrant size transcripts. Thus, the DRT gene may play a part in neuroblastoma and SCLC tumorigenesis.

Original languageEnglish (US)
Pages (from-to)2033-2045
Number of pages13
JournalHuman Molecular Genetics
Volume4
Issue number11
DOIs
StatePublished - Nov 1995
Externally publishedYes

Fingerprint

Protein Kinase
Protein-Tyrosine Kinases
Neuroblastoma
Genes
Cells
Gene
Brain
Proteins
Small Cell Lung Carcinoma
Lung
Cell
Tissue
Chromosomes
Cell Line
EphB2 Receptors
Tumors
Screening
Teratocarcinoma
Neural Plate
Kidney

ASJC Scopus subject areas

  • Statistics, Probability and Uncertainty
  • Applied Mathematics
  • Public Health, Environmental and Occupational Health
  • Molecular Biology
  • Genetics(clinical)
  • Genetics

Cite this

Molecular characterization and chromosomal localization of DRT (EPHT3) : A developmentally regulated human protein - tyrosine kinase gene of the EPH family. / Ikegaki, Naohiko; Tang, Xao X.; Liu, Xing Ge; Biegel, Jaclyn A.; Allen, Cindy; Yoshioka, Akira; Sulman, Erik P.; Brodeur, Garrett M.; Pleasure, David E.

In: Human Molecular Genetics, Vol. 4, No. 11, 11.1995, p. 2033-2045.

Research output: Contribution to journalArticle

Ikegaki, Naohiko ; Tang, Xao X. ; Liu, Xing Ge ; Biegel, Jaclyn A. ; Allen, Cindy ; Yoshioka, Akira ; Sulman, Erik P. ; Brodeur, Garrett M. ; Pleasure, David E. / Molecular characterization and chromosomal localization of DRT (EPHT3) : A developmentally regulated human protein - tyrosine kinase gene of the EPH family. In: Human Molecular Genetics. 1995 ; Vol. 4, No. 11. pp. 2033-2045.
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abstract = "By screening a human fetal brain cDNA expression library using a monocional antiphosphotyrosine antibody and by 5' RACE procedures, we have isolated overlapping cDNAs encoding a receptor-type tyrosine kinase belonging to the EPH family, DRT (Developmentally Regulated EPH-related Tyrosine kinase gene). The DRT gene is expressed in three different size transcripts (i.e. 4, 5 and 11 kb). DRT transcripts are expressed in human brain and several other tissues, including heart, lung, kidney, placenta, pancreas, liver and skeletal muscle, but the 11 kb DRT transcript is preferentially expressed in fetal brain. Steady-state levels of DRT mRNA in several tissues, including brain, heart, lung and kidney, are greater in the midterm fetus than those in the adult. DRT transcripts are detectable at low levels in a human teratocarcinoma cell line (NTera-2), but its expression is greatly increased after the NTera-2 cells are induced to become postmitotic neurons (NTera-2N) by retinoic acid treatment. These data suggest that DRT plays a part in human neurogenesis. A large number of tumor cell lines derived from neuroectoderm express DRT transcripts, including 12 neuroblastomas, two medulloblastomas, one primitive neuroectodermal tumor and six small cell lung carcinomas (SCLC). Interestingly, several neuroblastoma cell lines with 1p deletion and one SCLC cell line express DRT transcripts of aberrant size (i.e. 3, 6 and 8 kb) in addition to those found in normal tissues. We mapped the DRT gene to human chromosome 1p35-1p36.1 by PCR screening of human-rodent somatic cell hybrid panels and by fluorescence in situ hybridization. As the distal end of chromosome 1p is often deleted in neuroblastomas and altered in some cases in SCLCs, these chromosomal abnormalities may have resulted in the generation of aberrant size transcripts. Thus, the DRT gene may play a part in neuroblastoma and SCLC tumorigenesis.",
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AU - Liu, Xing Ge

AU - Biegel, Jaclyn A.

AU - Allen, Cindy

AU - Yoshioka, Akira

AU - Sulman, Erik P.

AU - Brodeur, Garrett M.

AU - Pleasure, David E

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