Significant correlation between the breakpoints of rare clonal aberrations in benign solid tumors and the assignment of HMGIY retropseudogenes

Cancer Genetics and Cytogenetics

Volumn 130, Issue 1, 2001, Pages 51-56

  Rogalla, Piere ^a   Blank, Cornelia ^a   Helbig, Roger ^a   Wosniok, Werner ^a   Bullerdiek, Jörn ^a  

^a UNIVERSITY OF BREMEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

HIGH MOBILITY GROUP PROTEIN;

ARTICLE; BENIGN TUMOR; CHROMOSOME 12Q; CHROMOSOME 4Q; CHROMOSOME ABERRATION; CHROMOSOME BREAKAGE; CHROMOSOME XP; DATA BASE; EXON; FLUORESCENCE IN SITU HYBRIDIZATION; GENE ACTIVATION; GENE MAPPING; HUMAN; HUMAN CELL; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PSEUDOGENE; RETROPSEUDOGENE; SEQUENCE ANALYSIS; SOLID TUMOR;

BASE SEQUENCE; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, ARTIFICIAL; HIGH MOBILITY GROUP PROTEINS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MOLECULAR SEQUENCE DATA; NEOPLASMS; PSEUDOGENES; SEQUENCE HOMOLOGY, NUCLEIC ACID; X CHROMOSOME;

EID: 0035475581     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(01)00452-6     Document Type: Article

References (26)

1. Back to the roots of a new exon-the molecular archaeology of a SP100 splice variant
2. High-mobility-group chromosomal proteins; architectural components that facilitate chromatin function
3. Disruption of the architectural factor HMGI-C; DNA-binding AT hook motifs fused in lipomas to distinct transcriptional regulatory domains
4. Recurrent rearrangements in the high mobility group protein gene, HMGI-C, in benign mesenchymal tumours
5. HMGI-C rearrangements as the molecular basis for the majority of pulmonary chondroid hamartomas; a survey of 30 tumors
6. Ten pulmonary chondroid hamartomas with chromosome 6p21 breakpoints within the HMGI-I(Y) or its immediate surroundings
7. HMGI(Y) expression in human uterine leiomyomata
8. A novel high mobility group protein gene is a candidate for Xp22 abnormalities in uterine leiomyomas and other benign tumors
9. Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization
10. Cloning of cDNA coding human HMGI and HMGY proteins; both are capable of binding to the octamer sequence motif
11. Gapped BLAST and PSI-BLAST; a new generation of protein database search programs
12. Results of cytogenetic analyses on 317 pulmonary chondroid hamartomas point to their pathogenesis
13. Promoter swapping between the genes for a novel zinc finger protein and beta-catenin in pleiomorphic adenomas with t(3;8)(p21;q12) translocations
14. Refined mapping of the region of loss of heterozygosity on the long arm of chromosome 7 in human breast cancer defines the location of a second tumor suppressor gene at 7q22 in the region of the CUTL1 gene
15. A uterine leiomyoma showing both t(12;14) and del(7) abnormalities
16. Testing the nonrandomness of chromosomal breakpoints using highest observed breakages
17. Organization, inducible-expression and chromosome localization of the human HMG-1(Y) nonhistone protein
18. A breakpoint map of recurrent chromosomal rearrangements in human neoplasia
19. Splice variants of the nuclear dot-associated Sp100 protein contain homologies to HMG-1 and a human nuclear phosphoprotein-box motif
20. Increased expression of high mobility group protein I(Y) in high grade prostatic cancer determined by in situ hybridization
21. The expression of the high mobility group HMGI(Y) proteins correlates with the malignant phenotype of human thyroid neoplasias
22. Human colorectal carcinomas express high levels of high mobility group HMGI(Y) proteins
23. A retrospective study of high mobility group protein I(Y) as progression marker for prostate cancer determined by in situ hybridization
24. Expression of HMGI(Y) proteins in squamous intraepithelial and invasive lesions of the uterine cervix