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International Journal of Molecular Medicine
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Print ISSN: 1107-3756 Online ISSN: 1791-244X
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October 2003 Volume 12 Issue 4

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International Journal of Molecular Medicine

International Journal of Molecular Medicine

International Journal of Molecular Medicine is an international journal devoted to molecular mechanisms of human disease.

International Journal of Oncology

International Journal of Oncology

International Journal of Oncology is an international journal devoted to oncology research and cancer treatment.

Molecular Medicine Reports

Molecular Medicine Reports

Covers molecular medicine topics such as pharmacology, pathology, genetics, neuroscience, infectious diseases, molecular cardiology, and molecular surgery.

Oncology Reports

Oncology Reports

Oncology Reports is an international journal devoted to fundamental and applied research in Oncology.

Experimental and Therapeutic Medicine

Experimental and Therapeutic Medicine

Experimental and Therapeutic Medicine is an international journal devoted to laboratory and clinical medicine.

Oncology Letters

Oncology Letters

Oncology Letters is an international journal devoted to Experimental and Clinical Oncology.

Biomedical Reports

Biomedical Reports

Explores a wide range of biological and medical fields, including pharmacology, genetics, microbiology, neuroscience, and molecular cardiology.

Molecular and Clinical Oncology

Molecular and Clinical Oncology

International journal addressing all aspects of oncology research, from tumorigenesis and oncogenes to chemotherapy and metastasis.

World Academy of Sciences Journal

World Academy of Sciences Journal

Multidisciplinary open-access journal spanning biochemistry, genetics, neuroscience, environmental health, and synthetic biology.

International Journal of Functional Nutrition

International Journal of Functional Nutrition

Open-access journal combining biochemistry, pharmacology, immunology, and genetics to advance health through functional nutrition.

International Journal of Epigenetics

International Journal of Epigenetics

Publishes open-access research on using epigenetics to advance understanding and treatment of human disease.

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Article

Identification and characterization of human FNBP3 gene in silico

  • Authors:
    • Masuko Katoh
    • Masaru Katoh
  • View Affiliations / Copyright

    Affiliations: M&M Medical BioInformatics, Narashino 275-0022, Japan
  • Pages: 651-656
    |
    Published online on: October 1, 2003
       https://doi.org/10.3892/ijmm.12.4.651
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Abstract

FMNL1, FMNL2, FMNL3, DAAM1, DAAM2, DIAPH1 and DIAPH2 constitute the Formin-homology subfamily with FDD, FH1 and FH2 domains. FMNL2 gene is linked to FNBP3 (also known as HYPA) gene on human chromosome 2q23.3, while FMNL3 gene to FNBP3L (also known as HYPC) gene on 12q13. Because human FNBP3 cDNA (NM_017892.2) was a 5'-truncated partial clone, we identified and characterized human FNBP3 gene by using bioinformatics. Human FNBP3 gene, consisting of 26 exons, was located within human genome sequences AC079344.5, AC012443.8, and human chromosome 2 genomic contig NT_005403.13. Nucleotide sequence of human FNBP3 cDNA was determined in silico by assembling nucleotide sequences of 26 exons of FNBP3 gene. HYPA cDNA and IMAGE cDNA clones 3356968, 4026200, 4733897 were 3'-truncated partial FNBP3 cDNAs, while FNBP3 (NM_017892.2), FLJ11559, NY-REN-6, and FLJ20585 were 5'-truncated partial FNBP3 cDNAs. Two FNBP3 isoforms with or without 126-bp region in the 3'-part of exon 1 were transcribed due to alternative splicing. FNBP3 isoform 2 without the 126-bp region was the major FNBP3 transcript. Two WW domains, two FF domains, two bipartite nuclear localization signals, FB3HM and FB3HC domains were conserved among vertebrate FNBP3 homologs, including human FNBP3, FNBP3L, mouse Fnbp3, Fnbp3l, chicken fnbp3 and zebrafish fnbp3. FNBP3, binding to TNFSF6 (Fas ligand), Huntingtin and Formin proteins, might transduce extracellular signals to the Rho-related signaling pathway. On the other hand, FNBP3 with nuclear localization signals and two tyrosine phosphorylation sites might transduce extracellular signals to the nucleus. This is the first report on comprehensive characterization of human FNBP3 gene.

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Copy and paste a formatted citation
Spandidos Publications style
Katoh M and Katoh M: Identification and characterization of human FNBP3 gene in silico. Int J Mol Med 12: 651-656, 2003.
APA
Katoh, M., & Katoh, M. (2003). Identification and characterization of human FNBP3 gene in silico. International Journal of Molecular Medicine, 12, 651-656. https://doi.org/10.3892/ijmm.12.4.651
MLA
Katoh, M., Katoh, M."Identification and characterization of human FNBP3 gene in silico". International Journal of Molecular Medicine 12.4 (2003): 651-656.
Chicago
Katoh, M., Katoh, M."Identification and characterization of human FNBP3 gene in silico". International Journal of Molecular Medicine 12, no. 4 (2003): 651-656. https://doi.org/10.3892/ijmm.12.4.651
Copy and paste a formatted citation
x
Spandidos Publications style
Katoh M and Katoh M: Identification and characterization of human FNBP3 gene in silico. Int J Mol Med 12: 651-656, 2003.
APA
Katoh, M., & Katoh, M. (2003). Identification and characterization of human FNBP3 gene in silico. International Journal of Molecular Medicine, 12, 651-656. https://doi.org/10.3892/ijmm.12.4.651
MLA
Katoh, M., Katoh, M."Identification and characterization of human FNBP3 gene in silico". International Journal of Molecular Medicine 12.4 (2003): 651-656.
Chicago
Katoh, M., Katoh, M."Identification and characterization of human FNBP3 gene in silico". International Journal of Molecular Medicine 12, no. 4 (2003): 651-656. https://doi.org/10.3892/ijmm.12.4.651
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