Cloning and characterization of a novel human gene RNF38 encoding a conserved putative protein with a RING finger domain

Biochemical and Biophysical Research Communications

Volumn 294, Issue 5, 2002, Pages 1169-1176

  Eisenberg, Iris ^a   Hochner, Hagit ^a   Levi, Tatjana ^b   Yelin, Rodrigo ^c   Kahan, Tamar ^d   Mitrani Rosenbaum, Stella ^a  

^a HEBREW UNIVERSITY   (Israel)

^b HARVARD MEDICAL SCHOOL   (United States)

^c Compugen Ltd ^*  (Israel)

^d HEBREW UNIVERSITY OF JERUSALEM   (Israel)

Author keywords

Chromosome 9; Genomic structure; RING finger motif; RING H2; RNF38

Indexed keywords

BINDING PROTEIN; MESSENGER RNA; PROLINE; REALLY INTERESTING NEW GENE FINGER PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; CARBOXY TERMINAL SEQUENCE; CARCINOMA; CHROMOSOME 9P; CONTROLLED STUDY; EXON; GENE EXPRESSION; GENE FUNCTION; GENE STRUCTURE; GENETIC CONSERVATION; GENOME ANALYSIS; HUMAN; HUMAN TISSUE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN MOTIF; RNA ANALYSIS; SEQUENCE HOMOLOGY; SPECIES COMPARISON; TESTIS; TISSUE DISTRIBUTION;

AMINO ACID SEQUENCE; CARRIER PROTEINS; CHROMOSOME MAPPING; CLONING, MOLECULAR; CONSERVED SEQUENCE; DNA MUTATIONAL ANALYSIS; HUMANS; MOLECULAR SEQUENCE DATA; PROTEIN STRUCTURE, TERTIARY; PROTEINS; RATS; RNA, MESSENGER; SEQUENCE ALIGNMENT; TISSUE DISTRIBUTION;

DROSOPHILA MELANOGASTER; MELANOGASTER; MUS; MUS MUSCULUS; MUSCULUS; RATTUS; RATTUS NORVEGICUS;

EID: 0036292537     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-291X(02)00584-3     Document Type: Article

References (40)

1. RING domains: Master builders of molecular scaffolds?
2. Does this have a familiar RING?
3. Novel cysteine-rich sequence motif
4. Structure of the C3HC4 domain by 1H-nuclear magnetic resonance spectroscopy. A new structural class of zinc-finger
5. The RING finger. A novel protein sequence motif related to the zinc finger
6. RING fingers mediate ubiquitin-conjugating enzyme (E2)-dependent ubiquitination
7. RING for destruction?
8. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
9. The truncation that generated the v-Cbl oncogene reveals an ability for nuclear transport, DNA binding and acute transformation
10. Physical association between Src homology 3 elements and the protein product of the c-Cbl proto-oncogene
11. The solution structure of the RING finger domain from the acute promyelocytic leukaemia proto-oncoprotein PML
12. The N-terminal part of TIF1, a putative mediator of the ligand-dependent activation function (AF-2) of nuclear receptors, is fused to B-raf in the oncogenic protein T18
13. Identification of three distinct tumor suppressor loci on the short arm of chromosome 9 in small cell lung cancer
14. Frequent allelic loss on chromosome 9 in hepatocellular carcinoma
15. Allelic loss at the D9S171 locus on chromosome 9p13 is associated with progression of papillary renal cell carcinoma
16. MPT Collaborators, No germline mutations in CDKN2A (p16) in patients with squamous cell cancer of the head and neck and second primary tumours
17. Karyotypic characterization of urinary bladder transitional cell carcinomas
18. Evidence for three tumor suppressor loci on chromosome 9p involved in melanoma development
19. The paired box domain gene PAX5 is fused to ETV6/TEL in an acute lymphoblastic leukemia case
20. High frequency of deletion on chromosome 9p21 may harbor several tumor-suppressor genes in human prostate cancer
21. Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13
22. The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy
23. Increased exon-trapping efficiency through modifications to the pSPL3 splicing vector
24. Isolation of genes from complex sources of mammalian genomic DNA using exon amplification
25. Gapped BLAST and PSI-BLAST: A new generation of protein database search programs
26. Hereditary inclusion body myopathy maps to chromosome 9p1-q1
27. The InterPro database, an integrated documentation resource for protein families domains and functional sites
28. Inverse single-strand RACE: An adapter-independent method of 5′ RACE
29. The scanning model for translation: An update
30. High altitude termination. Regulation of transcription elongation and termination: A Keystone Symposium, Keystone, CO, April 19-25, 1991
31. Analysis of canonical and non-canonical splice sites in mammalian genomes
32. Chromosomal location and some structural features of human clathrin light-chain genes (CLTA and CLTB)
33. Prediction of the coding sequences of unidentified human genes. V. The coding sequences of 40 new genes (KIAA0161-KIAA0200) deduced by analysis of cDNA clones from human cell line KG-1
34. Cloning and characterization of RNF6, a novel RING finger gene mapping to 13q12
35. Predicting coiled coils from protein sequences
36. A gene for distal arthrogryposis type I maps to the pericentromeric region of chromosome 9
37. Acromesomelic dysplasia Maroteaux type maps to human chromosome
38. A gene for ataxic cerebral palsy maps to chromosome 9p12-q12
39. Distal hereditary motor neuropathy of the Jerash type