Molecular cloning and characterization of OSR1 on human chromosome 2p24

Int J Mol Med. 2002 Aug;10(2):221-5.

Abstract

During Drosophila hindgut development, bowl, caudal/CDX, brachyenteron/Brachyury/TBX, fork head/FOX, drumstick, lines, and wingless/WNT play important roles. Drosophila bowl gene is homologous to Drosophila odd-skipped (odd) gene and odd-skipped related gene (sob). Here, human OSR1, related to Drosophila odd, was isolated using bioinformatics and cDNA-PCR. OSR1 was found to encode 266 amino-acid protein with three C2H2-type zinc fingers, a tyrosine phosphorylation site (Tyr 203), and several putative PXXP SH3 binding motifs. Three zinc fingers and a tyrosine phosphorylation site were conserved among human OSR1, OSR2, Drosophila odd, sob, and bowl. OSR1 showed 63.6% total amino-acid identity with OSR2. OSR1 gene consisting of three exons was located on human chromosome 2p24. OSR1 mRNA of 2.3-kb in size was detected in adult colon, small intestine, prostate, testis, and fetal lung. OSR1 mRNA was significantly up-regulated in a pancreatic cancer cell line MIA PaCa-2, and was weakly expressed in gastric cancer cell lines OKAJIMA, MKN45, pancreatic cancer cell lines PANC-1, BxPC-3, AsPC-1, PSN-1, Hs766T, and esophageal cancer cell line TE10. Among 10 cases of primary gastric cancer, OSR1 mRNA was up-regulated in 5 cases, and was down-regulated in 2 cases. This is the first report on molecular cloning and characterization of human OSR1.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Motifs
  • Animals
  • Chromosome Mapping
  • Chromosomes, Human, Pair 2 / genetics*
  • Cloning, Molecular
  • DNA-Binding Proteins / genetics
  • Digestive System / metabolism
  • Digestive System Neoplasms / metabolism
  • Digestive System Neoplasms / pathology
  • Drosophila Proteins / genetics
  • Drosophila melanogaster / genetics
  • Exons / genetics
  • Genes*
  • Humans
  • Lung / embryology
  • Lung / metabolism
  • Male
  • Neoplasm Proteins / biosynthesis
  • Neoplasm Proteins / genetics
  • Organ Specificity
  • Phosphorylation
  • Prostate / metabolism
  • Protein Processing, Post-Translational
  • Protein Serine-Threonine Kinases / biosynthesis
  • Protein Serine-Threonine Kinases / genetics*
  • RNA, Messenger / biosynthesis
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Species Specificity
  • Testis / metabolism
  • Transcription Factors / genetics
  • Tumor Cells, Cultured / metabolism
  • Zinc Fingers / genetics
  • src Homology Domains

Substances

  • DNA-Binding Proteins
  • Drosophila Proteins
  • Neoplasm Proteins
  • RNA, Messenger
  • Sob protein, Drosophila
  • Transcription Factors
  • bowl protein, Drosophila
  • odd protein, Drosophila
  • OXSR1 protein, human
  • Protein Serine-Threonine Kinases