Home LiteratureArticle Details
PMID: 11856480 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Expression of Hqk encoding a KH RNA binding protein is altered in human glioma.

Japanese journal of cancer research : Gann ·Vol. 93 ·No. 2 ·2002-02-00 ·Pages 167-77

Li ZZ, Kondo T, Murata T, Ebersole TA, Nishi T, Tada K, Ushio Y, Yamamura K, Abe K

Abstract

The quaking gene family encodes single KH domain RNA-binding proteins that play vital roles in cell differentiation, proliferation, and apoptotic processes. The human quaking gene, Hqk, maps to 6q25-q26, where cytogenetic alterations associated with a variety of human malignancies, including gliomas have been reported. To assess possible relationships of Hqk with human diseases such as glial tumors, we first isolated the Hqk gene, characterized its structure and expression pattern, and carried out mutational analysis of Hqk in primary tumor samples. The Hqk gene contains 8 exons spanning a approximately 200 kb genomic region, and generating at least four alternatively spliced transcripts, Hqk-5, Hqk-6, Hqk-7 and Hqk-7B, of which Hqk-7 is abundantly expressed in brain. Analysis of primary tumors demonstrated a high incidence of expression alterations of Hqk in gliomas (30%; 6/20), but not in other tumors such as schwannomas (0/3), or meningiomas (0/8). Among the tumor samples showing expression alterations, two were devoid of all three major transcripts, one was missing only the Hqk-5 message, and only the Hqk-7 message was absent in two cases. Our results thus imply the involvement of Hqk in human glial tumor progression.

MeSH Terms
Chromosome Mapping Cloning, Molecular Exons Gene Expression Regulation, Neoplastic Glioma/genetics Humans Introns RNA, Messenger/analysis RNA-Binding Proteins/genetics Reverse Transcriptase Polymerase Chain Reaction
Chemicals
QKI protein, human Qk protein, mouse RNA, Messenger RNA-Binding Proteins
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Li Zheng Zhe
Department of Developmental Genetics, Institute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto 862-0976, Japan.
Kondo Tatsuya
Murata Tomoaki
Ebersole Thomas A
Nishi Toru
Tada Kenji
Ushio Yukitaka
Yamamura Ken-ichi
Abe Kuniya
References (39)
39 references, click to expand
  1. Molecular defects in the dysmyelinating mutant quaking.
    J Neurosci Res. 1998 Feb 15;51(4):417-22 PMID: 9514195
  2. Cloning of a full-length complementary DNA for an Artemia salina glycine-rich protein. Structural relationship with RNA binding proteins.
    J Biol Chem. 1987 Oct 5;262(28):13377-80 PMID: 2443491
  3. FMR1 protein: conserved RNP family domains and selective RNA binding.
    Science. 1993 Oct 22;262(5133):563-6 PMID: 7692601
  4. The pre-mRNA binding K protein contains a novel evolutionarily conserved motif.
    Nucleic Acids Res. 1993 Mar 11;21(5):1193-8 PMID: 8464704
  5. Genomic organization and expression analysis of the mouse qkI locus.
    Mamm Genome. 1999 Jul;10(7):662-9 PMID: 10384037
  6. Expression of the neural RNA-binding protein Musashi1 in human gliomas.
    Glia. 2001 Apr 1;34(1):1-7 PMID: 11284014
  7. Tumorigenicity in human melanoma cell lines controlled by introduction of human chromosome 6.
    Science. 1990 Feb 2;247(4942):568-71 PMID: 2300817
  8. The held out wings (how) Drosophila gene encodes a putative RNA-binding protein involved in the control of muscular and cardiac activity.
    Development. 1997 May;124(10 ):2087-98 PMID: 9169854
  9. The quaking gene product necessary in embryogenesis and myelination combines features of RNA binding and signal transduction proteins.
    Nat Genet. 1996 Mar;12(3):260-5 PMID: 8589716
  10. Multiple deleted regions on the long arm of chromosome 6 in astrocytic tumours.
    Br J Cancer. 2000 Feb;82(3):543-9 PMID: 10682663
  11. Cloning of a gene highly overexpressed in cancer coding for a novel KH-domain containing protein.
    Oncogene. 1997 Jun 5;14(22):2729-33 PMID: 9178771
  12. Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines.
    Cancer Res. 1997 Mar 1;57(5):808-11 PMID: 9041175
  13. gld-1, a tumor suppressor gene required for oocyte development in Caenorhabditis elegans.
    Genetics. 1995 Feb;139(2):579-606 PMID: 7713419
  14. Neural cell type-specific expression of QKI proteins is altered in quakingviable mutant mice.
    J Neurosci. 1996 Dec 15;16(24):7941-9 PMID: 8987822
  15. Molecular cloning and nucleic acid binding properties of the GAP-associated tyrosine phosphoprotein p62.
    Cell. 1992 May 1;69(3):551-8 PMID: 1374686
  16. Mutations in gld-1, a female germ cell-specific tumor suppressor gene in Caenorhabditis elegans, affect a conserved domain also found in Src-associated protein Sam68.
    Genes Dev. 1995 Jun 15;9(12):1491-504 PMID: 7601353
  17. A point mutation in the FMR-1 gene associated with fragile X mental retardation.
    Nat Genet. 1993 Jan;3(1):31-5 PMID: 8490650
  18. GLD-1, a cytoplasmic protein essential for oocyte differentiation, shows stage- and sex-specific expression during Caenorhabditis elegans germline development.
    Dev Biol. 1996 Nov 25;180(1):165-83 PMID: 8948583
  19. who encodes a KH RNA binding protein that functions in muscle development.
    Development. 1997 Apr;124(7):1323-32 PMID: 9118803
  20. MCG10, a novel p53 target gene that encodes a KH domain RNA-binding protein, is capable of inducing apoptosis and cell cycle arrest in G(2)-M.
    Mol Cell Biol. 2000 Aug;20(15):5602-18 PMID: 10891498
  21. PipMaker--a web server for aligning two genomic DNA sequences.
    Genome Res. 2000 Apr;10(4):577-86 PMID: 10779500
  22. A mitotic function for Src?
    Trends Cell Biol. 1994 Oct;4(10):345-7 PMID: 14731619
  23. Three ENU-induced alleles of the murine quaking locus are recessive embryonic lethal mutations.
    Genet Res. 1988 Apr;51(2):95-102 PMID: 3410318
  24. Evidence of allelic imbalance of chromosome 6 in human astrocytomas.
    Neurology. 1994 Mar;44(3 Pt 1):533-6 PMID: 7908424
  25. The KH domain occurs in a diverse set of RNA-binding proteins that include the antiterminator NusA and is probably involved in binding to nucleic acid.
    FEBS Lett. 1993 Jun 21;324(3):361-6 PMID: 8405383
  26. Analysis of the multiple roles of gld-1 in germline development: interactions with the sex determination cascade and the glp-1 signaling pathway.
    Genetics. 1995 Feb;139(2):607-30 PMID: 7713420
  27. Three-dimensional structure and stability of the KH domain: molecular insights into the fragile X syndrome.
    Cell. 1996 Apr 19;85(2):237-45 PMID: 8612276
  28. The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein.
    Cell. 1993 Jul 30;74(2):291-8 PMID: 7688265
  29. Nuclear translocation controlled by alternatively spliced isoforms inactivates the QUAKING apoptotic inducer.
    Genes Dev. 2001 Apr 1;15(7):845-58 PMID: 11297509
  30. STAR, a gene family involved in signal transduction and activation of RNA.
    Trends Genet. 1997 Dec;13(12 ):479-84 PMID: 9433137
  31. An RNA-binding protein associated with Src through its SH2 and SH3 domains in mitosis.
    Nature. 1994 Apr 28;368(6474):867-71 PMID: 7512694
  32. MUTANT MICE (QUAKING AND JIMPY) WITH DEFICIENT MYELINATION IN THE CENTRAL NERVOUS SYSTEM.
    Science. 1964 Apr 17;144(3616):309-11 PMID: 14169723
  33. Remarkable sequence conservation of transcripts encoding amphibian and mammalian homologues of quaking, a KH domain RNA-binding protein.
    Gene. 1997 Apr 1;188(2):199-206 PMID: 9133592
  34. Hypomyelination in the quaking mouse. A model for the analysis of disturbed myelin formation.
    J Neuropathol Exp Neurol. 1970 Oct;29(4):507-23 PMID: 5471919
  35. Essential role for KH domains in RNA binding: impaired RNA binding by a mutation in the KH domain of FMR1 that causes fragile X syndrome.
    Cell. 1994 Apr 8;77(1):33-9 PMID: 8156595
  36. The KH domain protein encoded by quaking functions as a dimer and is essential for notochord development in Xenopus embryos.
    Genes Dev. 1997 Sep 1;11(17):2176-90 PMID: 9303534
  37. A breakpoint map of recurrent chromosomal rearrangements in human neoplasia.
    Nat Genet. 1997 Apr;15 Spec No:417-74 PMID: 9140409
  38. KH domains within the FMR1 sequence suggest that fragile X syndrome stems from a defect in RNA metabolism.
    Trends Biochem Sci. 1993 Sep;18(9):331-3 PMID: 7694397
  39. A novel cytoplasmic protein with RNA-binding motifs is an autoantigen in human hepatocellular carcinoma.
    J Exp Med. 1999 Apr 5;189(7):1101-10 PMID: 10190901
Article Info
Journal
Japanese journal of cancer research : Gann
Abbr.
Jpn J Cancer Res
ISSN
0910-5050
Published
2002-02-00
Pages
167-77
Language
English
Region
Japan
NLM ID
8509412
PMCID
PMC5926958
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com