Characterization of Bcor expression in mouse development

Gene Expression Patterns

Volumn 7, Issue 5, 2007, Pages 550-557

  Wamstad, Joseph A ^a   Bardwell, Vivian J ^a,b  

^a Molecular   (United States)

^b Cancer Center   (United States)

Author keywords

AF9; BCL6; Bcor; Extraembryonic; Lenz; MCOPS2; Oculofaciocardiodental syndrome; OFCD; PcG

Indexed keywords

MIXED LINEAGE LEUKEMIA PROTEIN; PROTEIN BCL 6; PROTEIN BCOR; REPRESSOR PROTEIN; UNCLASSIFIED DRUG;

5' UNTRANSLATED REGION; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN TISSUE; BRANCHIAL ARCH; CONGENITAL HEART MALFORMATION; CONTROLLED STUDY; CORRELATION ANALYSIS; CRANIOFACIAL MALFORMATION; DISEASE SEVERITY; EMBRYO; EMBRYO DEVELOPMENT; EMBRYONAL TISSUE; EXON; EYE; EYE MALFORMATION; FETUS DEVELOPMENT; FINGER MALFORMATION; GASTRULATION; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION; GENE MUTATION; GENETIC ANALYSIS; GESTATION PERIOD; IN SITU HYBRIDIZATION; MALFORMATION SYNDROME; MOUSE; NERVOUS SYSTEM DEVELOPMENT; NEURAL TUBE; NONHUMAN; NUCLEOTIDE SEQUENCE; OCULOFACIOCARDIODENTAL SYNDROME; ORGANOGENESIS; PRIORITY JOURNAL; PROMOTER REGION; SURVIVAL RATE; TISSUE TYPES; TRANSCRIPTION INITIATION; TRANSCRIPTION REGULATION; X CHROMOSOME LINKED DISORDER;

ANIMALS; BLOTTING, NORTHERN; DNA-BINDING PROTEINS; GENE EXPRESSION REGULATION, DEVELOPMENTAL; IN SITU HYBRIDIZATION; MICE; PROMOTER REGIONS (GENETICS); PROTO-ONCOGENE PROTEINS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA PROBES; RNA SPLICING; RNA, MESSENGER; TISSUE DISTRIBUTION;

MUS;

EID: 33947502436     PISSN: 1567133X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.modgep.2007.01.006     Document Type: Article

References (20)

1. Ausubel, F.M., 1988. Current protocols in molecular biology (New York: Greene Pub. Associates; Wiley-Interscience), pp. v. (loose-leaf).
2. Baron B.W., Nucifora G., McCabe N., Espinosa III R., Le Beau M.M., and McKeithan T.W. Identification of the gene associated with the recurring chromosomal translocations t(3;14)(q27;q32) and t(3;22)(q27;q11) in B-cell lymphomas. Proc. Natl. Acad. Sci. USA 90 (1993) 5262-5266
3. Cattoretti G., Pasqualucci L., Ballon G., Tam W., Nandula S.V., Shen Q., Mo T., Murty V.V., and Dalla-Favera R. Deregulated BCL6 expression recapitulates the pathogenesis of human diffuse large B cell lymphomas in mice. Cancer Cell 7 (2005) 445-455
4. Chen W., Iida S., Louie D.C., Dalla-Favera R., and Chaganti R.S. Heterologous promoters fused to BCL6 by chromosomal translocations affecting band 3q27 cause its deregulated expression during B-cell differentiation. Blood 91 (1998) 603-607
5. Collins E.C., Appert A., Ariza-McNaughton L., Pannell R., Yamada Y., and Rabbitts T.H. Mouse Af9 is a controller of embryo patterning, like Mll, whose human homologue fuses with Af9 after chromosomal translocation in leukemia. Mol. Cell. Biol. 22 (2002) 7313-7324
6. Dalla-Favera R., Migliazza A., Chang C.C., Niu H., Pasqualucci L., Butler M., Shen Q., and Cattoretti G. Molecular pathogenesis of B cell malignancy: the role of BCL-6. Curr. Top. Microbiol. Immunol. 246 (1999) 257-263 discussion 263-255
7. Gearhart M.D., Corcoran C.M., Wamstad J.A., and Bardwell V.J. Polycomb group and SCF ubiquitin ligases are found in a novel BCOR complex that is recruited to BCL6 targets. Mol. Cell. Biol. 26 (2006) 6880-6889
8. Hedera P., and Gorski J.L. Oculo-facio-cardio-dental syndrome: skewed X chromosome inactivation in mother and daughter suggest X-linked dominant Inheritance. Am. J. Med. Genet. A 123 (2003) 261-266
9. Horn D., Chyrek M., Kleier S., Luttgen S., Bolz H., Hinkel G.K., Korenke G.C., Riess A., Schell-Apacik C., Tinschert S., et al. Novel mutations in BCOR in three patients with oculo-facio-cardio-dental syndrome, but none in Lenz microphthalmia syndrome. Eur. J. Hum. Genet. 13 (2005) 563-569
10. Huynh K.D., Fischle W., Verdin E., and Bardwell V.J. BCoR, a novel corepressor involved in BCL-6 repression. Genes Dev. 14 (2000) 1810-1823
11. Kerckaert J.P., Deweindt C., Tilly H., Quief S., Lecocq G., and Bastard C. LAZ3, a novel zinc-finger encoding gene, is disrupted by recurring chromosome 3q27 translocations in human lymphomas. Nat. Genet. 5 (1993) 66-70
12. Miki T., Kawamata N., Arai A., Ohashi K., Nakamura Y., Kato A., Hirosawa S., and Aoki N. Molecular cloning of the breakpoint for 3q27 translocation in B-cell lymphomas and leukemias. Blood 83 (1994) 217-222
13. Nagase T., Kikuno R., Nakayama M., Hirosawa M., and Ohara O. Prediction of the coding sequences of unidentified human genes. XVIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. DNA Res. 7 (2000) 273-281
14. Nagy A. Manipulating the Mouse Embryo: A Laboratory Manual. third ed. (2003), Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
15. Ng D., Hadley D.W., Tifft C.J., and Biesecker L.G. Genetic heterogeneity of syndromic X-linked recessive microphthalmia-anophthalmia: is Lenz microphthalmia a single disorder?. Am. J. Med. Genet. 110 (2002) 308-314
16. Ng D., Thakker N., Corcoran C.M., Donnai D., Perveen R., Schneider A., Hadley D.W., Tifft C., Zhang L., Wilkie A.O., et al. Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR. Nat. Genet. 36 (2004) 411-416
17. Schulze B.R., Horn D., Kobelt A., Tariverdian G., and Stellzig A. Rare dental abnormalities seen in oculo-facio-cardio-dental (OFCD) syndrome: three new cases and review of nine patients. Am. J. Med. Genet. 82 (1999) 429-435
18. Srinivasan R.S., de Erkenez A.C., and Hemenway C.S. The mixed lineage leukemia fusion partner AF9 binds specific isoforms of the BCL-6 corepressor. Oncogene 22 (2003) 3395-3406
19. Ye B.H., Lista F., Lo Coco F., Knowles D.M., Offit K., Chaganti R.S., and Dalla-Favera R. Alterations of a zinc finger-encoding gene, BCL-6, in diffuse large-cell lymphoma. Science 262 (1993) 747-750
20. Ye B.H., Chaganti S., Chang C.C., Niu H., Corradini P., Chaganti R.S., and Dalla-Favera R. Chromosomal translocations cause deregulated BCL6 expression by promoter substitution in B cell lymphoma. EMBO J. 14 (1995) 6209-6217