HMG20A and HMG20B map to human chromosomes 15q24 and 19p13.3 and constitute a distinct class of HMG-box genes with ubiquitous expression

Cytogenetics and Cell Genetics

Volumn 88, Issue 1-2, 2000, Pages 62-67

  Sumoy, Lauro ^a   Carim, L ^a   Escarceller, M ^a   Nadal, M ^a   Gratacos M ^a   Pujana, M A ^a   Estivill, X ^a   Peral, B ^a  

^a HOSPITAL DURAN I REYNALS   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; HIGH MOBILITY GROUP PROTEIN;

ARTICLE; CHROMATIN; CHROMOSOME 15Q; CHROMOSOME 19P; DNA BINDING; GENE EXPRESSION; GENE MAPPING; GENE STRUCTURE; HUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; TRANSCRIPTION REGULATION; YEAST;

MAMMALIA;

EID: 0034067297     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: 10.1159/000015486     Document Type: Article

References (22)

1. Auffray C, Behar G, Bois F, Bouchier C, Da Silva C, Devignes MD, Duprat S, Houlgatte R, Jumeau MN, Lamy B, et al.: IMAGE: molecular integration of the analysis of the human genome and its expression. CR Acad Sci III 318:263-272 (1995).
2. Baxevanis AD, Landsman D: The HMG-1 box protein family: classification and functional relationships. Nucl Acids Res 23:1604-1613 (1995).
3. Blake JA, Richardson JE, Davisson MT, Eppig JT: The Mouse Genome Database (MGD): genetic and genomic information about the laboratory mouse. The Mouse Genome Database Group. Nucl Acids Res 27:95-98 (1999).
4. Bloom JL, Falconer DS: "Grizzled", a mutant in linkage group X of the mouse. Genet Res 7:159-167 (1966).
5. Collins FS, Patrinos A, Jordan E, Chakravarti A, Gesteland R, Walters L: New goals for the U.S. Human Genome Project: 1998-2003. Science 282:682-689 (1998).
6. Deloukas P, Schuler GD, Gyapay G, Beasley EM, Soderlund C, Rodriguez-Tome P, Hui L, Matise TC, McKusick KB, Beckmann JS, Bentolila S, Bihoreau M, Birren BB, Browne J, Butler A, Castle AB, Chiannilkulchai N, Clee C, Day PJ, Dehejia A, Dibling T, Drouot N, Duprat S, Fizames C, Bentley DR, et al: A physical map of 30,000 human genes. Science 282:744-746 (1998).
7. Grosschedl R, Giese K, Pagel J: HMG domain proteins: architectural elements in the assembly of nucleoprotein structures. Trends Genet 10:94-100 (1994).
8. Jantzen HM Admon A, Bell SP, Tjian R: Nucleolar transcription factor hUBF contains a DNA-binding motif with homology to HMG proteins. Nature 344:830-836 (1990).
9. Kapfhamer D, Sweet HO, Sufalko D, Warren S, Johnson KR, Burmeister M: The neurological mouse mutations jittery and hesitant are allelic and map to the region of mouse chromosome 10 homologous to 19p13.3. Genomics 35:533-538 (1996).
10. Kolodrubetz D, Burgum A: Duplicated NHP6 genes of Saccharomyces cerevisiae encode proteins homologous to bovine high mobility group protein I. J Biol Chem 265:3234-3239 (1990).
11. Landsman D, Bustin M: A signature for the HMG-1 box DNA-binding proteins. Bioessays 15:539-546 (1993).
12. Laudet V, Stehelin D, Clevers H: Ancestry and diversity of the HMG box superfamily. Nucl Acids Res 21:2493-2501 (1993).
13. Lennon G, Auffray C, Polymeropoulos M, Soares MB; The I.M.A.G.E. Consortium: an integrated molecular analysis of genomes and their expression. Genomics 33:151-152 (1996).
14. McKusick VA: Mendelian Inheritance in Man: Catalogs of Human Genes and Genetic Disorders. (Johns Hopkins University Press, Baltimore 1998).
15. Mitchell SJ, McHale DP, Campbell DA, Lench NJ, Mueller RF, Bundey SE, Markham AF: A syndrome of severe mental retardation, spasticity, and tapetoretinal degeneration linked to chromosome 15q24. Am J hum Genet 62:1070-1076 (1998).
16. Nadal M, Moreno S, Pritchard M, Preciado MA, Estivill X, Ramos-Arroyo MA: Down syndrome: characterisation of a case with partial trisomy of chromosome 21 owing to a paternal balanced translocation (15;21)(q26;q22.1) by FISH. J med Genet 34:50-54 (1997).
17. Paull TT, Haykinson MJ, Johnson RC: Yeast HMG proteins NHP6A/B potentiate promoter-specific transcriptional activation in vivo and assembly of preinitiation complexes in vitro. Genes Dev 7:1521-1534 (1993).
18. Phillips HA, Scheffer IE, Crossland KM, Bhatia KP, Fish DR, Marsden CD, Howell SJ, Stephenson JB, Tolmie J, Plazzi G, Eeg-Olofsson O, Singh R, Lopes-Cendes I, Andermann E, Andermann F, Berkovic SF, Mulley JC: Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24. Am J hum Genet 63:1108-1116 (1998).
19. Shows TB, Alper CA, Bootsma D, Dorf M, Douglas T, Huisman T, Kit S, Klinger HP, Kozak C, Lalley PA, Lindsley D, McAlpine PJ, McDougall JK, Meera Khan P, Meisler M, Morton NE, Opitz JM, Partridge CW, Payne R, Roderick TH, Rubinstein P, Ruddle FH, Shaw M, Spranger JW, Weiss K: International system for human gene nomenclature (1979): ISGN (1979). Cytogenet Cell Genet 25:96-116 (1979).
20. Soullier S, Jay P, Poulat F, Vanacker JM, Berta P, Laudet V: Diversification pattern of the HMG and SOX family members during evolution. J molec Evol 48:517-527 (1999).
21. Stewart EA, McKusick KB, Aggarwal A, Bajorek E, Brady S, Chu A, Fang N, Hadley D, Harris M, Hussain S, Lee R, Maratukulam A, O'Connor K, Perkins S, Piercy M, Qin F, Reif T, Sanders C, She X, Sun WL, Tabar P, Voyticky S, Cowles S, Fan JB, Cox DR, et al: An STS-based radiation hybrid map of the human genome. Genome Res 7:422-33 (1997).
22. Wang W, Chi T, Xue Y, Zhou S, Kuo A, Crabtree GR: Architectural DNA binding by a high-mobility-group/kinesin-like subunit in mammalian SWI/ SNF-related complexes. Proc natl Acad Sci, USA 95:492-498 (1998).