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International Journal of Oncology
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Print ISSN: 1019-6439 Online ISSN: 1791-2423
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March 2005 Volume 26 Issue 3

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Journals

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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Medicine International

An International Open Access Journal Devoted to General Medicine.

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March 2005 Volume 26 Issue 3

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Article

Identification and characterization of rat Wnt1 and Wnt10b genes in silico

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

    Affiliations: M&M Medical BioInformatics, Hongo 113-0033, Japan
  • Pages: 841-845
    |
    Published online on: March 1, 2005
       https://doi.org/10.3892/ijo.26.3.841
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Abstract

WNT family genes encode WNT family glycoproteins, while Frizzled (FZD) family genes encode seven-transmembrane-type receptors with extracellular WNT-binding domain and cytoplasmic Dishevelled-binding domain. WNT signaling pathway is implicated in carcinogenesis and embryogenesis. WNT1-WNT10B, WNT6-WNT10A, WNT3-WNT9B (WNT14B), WNT3A-WNT9A (WNT14) gene clusters exist within the human genome. Here, we identified and characterized rat Wnt1 and Wnt10b genes by using bioinformatics. Rat Wnt1 gene, consisting of four exons, encoded a 370-aa protein with signal peptide, 22 conserved Cys residues and four Asn-linked glycosylation sites. Rat Wnt10b gene, consisting of five exons, encoded a 389-aa protein with signal peptide, 24 conserved Cys residues and two Asn-linked glycosylation sites. Wnt1 and Wnt10b genes at rat chromosome 7q36 were clustered in head-to-head manner with an interval of about 10 kb within AC096835.4 or AC118760.4 genome sequences. Promoter region, exon 1 and 5'-part of intron 1 were conserved between rat and human Wnt1 orthologs. Intergenic conserved region (IGCR) was identified within the Wnt1-Wnt10b gene cluster. GC content of rat Wnt1-Wnt10b IGCR (nucleotide position 14962-15875 of AC096835.4 genome sequence) was 59.4%. Rat Wnt1-Wnt10b IGCR showed 92.5 and 74.4% nucleotide identity with mouse Wnt1-Wnt10b IGCR and human WNT1-WNT10B IGCR, respectively. Wnt1-Wnt10b IGCR was predicted as regulatory element rather than gene because cDNA or EST derived from Wnt1-Wnt10b IGCR was not identified. This is the first report on rat Wnt1 and Wnt10b genes as well as on Wnt1-Wnt10b IGCR.

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Copy and paste a formatted citation
Spandidos Publications style
Katoh Y and Katoh M: Identification and characterization of rat Wnt1 and Wnt10b genes in silico. Int J Oncol 26: 841-845, 2005.
APA
Katoh, Y., & Katoh, M. (2005). Identification and characterization of rat Wnt1 and Wnt10b genes in silico. International Journal of Oncology, 26, 841-845. https://doi.org/10.3892/ijo.26.3.841
MLA
Katoh, Y., Katoh, M."Identification and characterization of rat Wnt1 and Wnt10b genes in silico". International Journal of Oncology 26.3 (2005): 841-845.
Chicago
Katoh, Y., Katoh, M."Identification and characterization of rat Wnt1 and Wnt10b genes in silico". International Journal of Oncology 26, no. 3 (2005): 841-845. https://doi.org/10.3892/ijo.26.3.841
Copy and paste a formatted citation
x
Spandidos Publications style
Katoh Y and Katoh M: Identification and characterization of rat Wnt1 and Wnt10b genes in silico. Int J Oncol 26: 841-845, 2005.
APA
Katoh, Y., & Katoh, M. (2005). Identification and characterization of rat Wnt1 and Wnt10b genes in silico. International Journal of Oncology, 26, 841-845. https://doi.org/10.3892/ijo.26.3.841
MLA
Katoh, Y., Katoh, M."Identification and characterization of rat Wnt1 and Wnt10b genes in silico". International Journal of Oncology 26.3 (2005): 841-845.
Chicago
Katoh, Y., Katoh, M."Identification and characterization of rat Wnt1 and Wnt10b genes in silico". International Journal of Oncology 26, no. 3 (2005): 841-845. https://doi.org/10.3892/ijo.26.3.841
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