Assignment of the gene for a ubiquitin fusion degradation protein (Ufd1l) to mouse chromosome 16B1-B4, syntenic with the Tuple1 gene

Cytogenetics and Cell Genetics

Volumn 77, Issue 3-4, 1997, Pages 264-265

  Botta, A ^a   Jurecic, V ^a   Novelli, G ^b,c   Dallapiccola, B ^d   Baldini, A ^a,c,d  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF MILAN   (Italy)

^c Ospedale CSS   (Italy)

^d Cattedra di Genetica Umana   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CELL PROTEIN; HYBRID PROTEIN; PROTEINASE; UBIQUITIN;

ARTICLE; CHROMOSOME 16; GENE ASSIGNMENT; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEGRADATION; SYNTENY;

ANIMALS; CELL CYCLE PROTEINS; CHROMOSOME MAPPING; DNA PROBES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MICE; PROTEINS; TRANSCRIPTION FACTORS;

EID: 0030755247     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (7)

1. Baldini A, Lindsay EA: Mapping human YAC clones by fluorescence in situ hybridization using Alu-PCR from single yeast colonies, in Choo KHA (ed): In Situ Hybridization Protocols; Methods in Molecular Biology, Vol 33, pp 75-85 (Humana Press Inc., Clifton 1994).
2. Halford S, Wadey R, Roberts C, Daw SCM, Whiting JA, O'Donnell H, Dunham I, Bentley D, Lindsay EA, Baldini A, Francis F, Lehrach H, Williamson R, Wilson DI, Goodship J, Cross I, Burn J, Scambler PJ: Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease. Hum Mol Genet 2:2099-2107 (1993).
3. Johnson ES, Ma PCM, Ota IM, Varshasky A: A proteolytic pathway that recognizes ubiquitin as a degradation pathway. J biol Chem 270:17442-17456 (1995).
4. Lamour V, Lecluse Y, Desmaze C, Spector M, Bodescot M, Aurias A, Osley MA, Lipinski M: A human homolog of the S. cerevisiae HIR1 and HIR2 transcription repressors cloned from the DiGeorge syndrome critical region. Hum Mol Genet 4:791-799 (1995).
5. Mattei M-G, Halford S, Scambler PJ: Mapping of the Hira gene to mouse chromosome 16A-B1. Genomics 23:717-718 (1994).
6. Pizzuti A, Novelli G, Ratti A, Amati F, Mari A, Calabrese G, Nicolis S, Silani V, Marino B, Scarlato G, Ottolenghi S, Dallapiccola B: UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH22 syndrome. Hum Mol Genet 6:259-266 (1997).
7. Sambrook J, Fritsch EF, Maniatis T: Molecular cloning: A laboratory manual, 2nd ed (Cold Spring Harbor Laboratory Press, Cold Spring Harbor 1989).