Molecular cloning and characterization of a novel human gene (HERNA) which encodes a putative RNA-helicase

Biochimica et Biophysica Acta - Gene Structure and Expression

Volumn 1490, Issue 1-2, 2000, Pages 163-169

  Matsuda, Satoru ^a   Ichigotani, Yasukatu ^a   Okuda, Takahito ^a   Irimura, Tatsuro ^b   Nakatsugawa, Shigekazu ^c   Hamaguchi, Michinari ^a  

^a NAGOYA UNIVERSITY   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

^c NAGOYA UNIVERSITY HOSPITAL   (Japan)

Author keywords

Chromosome 14q31; RH mapping; RNA helicase; RNase

Indexed keywords

RIBONUCLEASE; RNA HELICASE;

AMINO TERMINAL SEQUENCE; ARTICLE; CAENORHABDITIS ELEGANS; CARBOXY TERMINAL SEQUENCE; CHROMOSOME 14Q; CHROMOSOME MAP; CONTROLLED STUDY; DNA SEQUENCE; ENZYME ANALYSIS; ENZYME LOCALIZATION; GENE ISOLATION; HUMAN; HUMAN CELL; HUMAN TISSUE; MOLECULAR CLONING; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; TISSUE DISTRIBUTION;

AMINO ACID SEQUENCE; BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 14; CLONING, MOLECULAR; DEAD-BOX RNA HELICASES; ENDORIBONUCLEASES; HUMANS; MOLECULAR SEQUENCE DATA; RNA HELICASES; SEQUENCE ALIGNMENT;

EID: 0033979493     PISSN: 01674781     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0167-4781(99)00221-3     Document Type: Article

References (20)

1. delaCruz J., Kressler D., Linder P. Unwinding RNA in Saccharomyces cerevisiae: DEAD-box proteins and related families. Trends Biochem. Sci. 24:1999;192-198.
2. Lohman T.M., Bjornson K.P. Mechanisms of helicase catalyzed DNA unwinding. Annu. Rev. Biochem. 65:1996;169-214.
3. Chang T.H., Arenas J., Abelson J. Identification of five putative yeast RNA helicase genes. Proc. Natl. Acad. Sci. USA. 87:1990;1571-1575.
4. Wassarman D.A., Steitz J.A. RNA splicing. Alive with DEAD proteins. Nature. 349:1991;463-464.
5. Eisen A., Sattah M., Gazitt T., Neal K., Szauter P., Lucchesi J. A novel DEAD-box RNA helicase exhibits high sequence conservation from yeast to humans. Biochim. Biophys. Acta. 1397:1998;131-136.
6. Kaghad M., Bonnet H., Yang A., Creancier L., Biscan J.-C., Valent A., Minty A., Chalon P., Lelias J.-M., Dumont X., Ferrara P., Mckeon F., Caput D. Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers. Cell. 90:1997;809-819.
7. Kuramochi S., Matsuda S., Matsuda Y., Saitoh T., Ohsugi M., Yamamoto T. Molecular cloning and characterization of Byp, a murine receptor-type tyrosine phosphatase similar to human DEP-1. FEBS Lett. 378:1996;7-14.
8. Matsuda S., Tsuzuku J.K., Ohsugi M., Yoshida M., Emi M., Nakamura Y., Onda M., Yoshida Y., Nishiyama A., Yamamoto T. Tob, a novel protein that interacts with p185erbB2, is associated with anti-proliferative activity. Oncogene. 12:1996;705-713.
9. Kozak M. The scanning model for translation: an update. J. Cell. Biol. 108:1989;229-241.
10. Provost P., Samuelsson B., Radmark O. Interaction of 5-lipoxygenase with cellular proteins. Proc. Natl. Acad. Sci. USA. 96:1999;1881-1885.
11. Ueki N., Seki N., Yano K., Masuho Y., Saito T., Muramatsu M. Isolation and characterization of a novel human gene (HFB30) which encodes a protein with a RING finger motif. Biochim. Biophys. Acta. 1445:1999;232-236.
12. Seki N., Hattori A., Hayashi A., Kozuma S., Ohira M., Hori T., Saito T. Structure, expression profile and chromosomal location of an isolog of DNA-PKcs interacting protein (KIP) gene. Biochim. Biophys. Acta. 1444:1999;143-147.
13. Jesionek-Kupnicka D., Majchrowska A., Krawczyk J., Wendorff J., Barcikowska M., Lukaszek S., Liberski P.P. Krabbe disease: an ultrastructural study of globoid cells and reactive astrocytes at the brain and optic nerves. Folia Neuropathol. 35:1997;155-162.
14. Cannizzaro L.A., Chen Y.Q., Rafi M.A., Wenger D.A. Regional mapping of the human galactocerebrosidase gene (GALC) to 14q31 by in situ hybridization. Cytogenet. Cell. Genet. 66:1994;244-245.
15. Xu Y., Casey G. Identification of human OGR1, a novel G protein-coupled receptor that maps to chromosome 14. Genomics. 35:1996;397-402.
16. Rousseau-Merck M.F., Misrahi M., Loosfelt H., Atger M., Milgrom E., Berger R. Assignment of the human thyroid stimulating hormone receptor (TSHR) gene to chromosome 14q31. Genomics. 8:1990;233-236.
17. Tomer Y., Barbesino G., Greenberg D.A., Concepcion E., Davies T.F. Linkage analysis of candidate genes in autoimmune thyroid disease. III. Detailed analysis of chromosome 14 localizes Graves' disease-1 GD-1) close to multinodular goiter-1 (MNG-1). International Consortium for the Genetics of Autoimmune Thyroid Disease. J. Clin. Endocrinol. Metab. 83:1998;4321-4327.
18. Tomer Y., Barbesino G., Keddache M., Greenberg D.A., Davies T.F. Mapping of a major susceptibility locus for Graves' disease (GD-1) to chromosome 14q31. J. Clin. Endocrinol. Metab. 82:1997;1645-1648.
19. deRoux N., Misrahi M., Chatelain N., Gross B., Milgrom E. Microsatellites and PCR primers for genetic studies and genomic sequencing of the human TSH receptor gene. Mol. Cell. Endocrinol. 117:1996;253-256.
20. O'Connell P., Fischbach K., Hilsenbeck S., Mohsin S.K., Fuqua S.A., Clark G.M., Osborne C.K., Allred D.C. Loss of heterozygosity at D14S62 and metastatic potential of breast cancer. J. Natl. Cancer Inst. 91:1999;1391-1397.