Cloning, functional study and comparative mapping of Luzp2 to mouse Chromosome 7 and human Chromosome 11p13-11p14

Mammalian Genome

Volumn 14, Issue 5, 2003, Pages 323-334

  Wu, Min ^a,b   Michaud, Edward J ^a   Johnson, Dabney K ^a  

^a OAK RIDGE NATIONAL LABORATORY   (United States)

^b WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

LEUCINE ZIPPER PROTEIN; LEUCINE ZIPPER PROTEIN 2; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ARTICLE; CHROMOSOME 11P; CHROMOSOME 7; GENE DELETION; GENE EXPRESSION; GENE FUSION; GENE MAPPING; GENE SEQUENCE; HUMAN; MOLECULAR CLONING; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; RADIATION HYBRID MAPPING; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY; WAGR SYNDROME;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; BLOTTING, NORTHERN; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 11; CLONING, MOLECULAR; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; DNA-BINDING PROTEINS; FEMALE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENE TARGETING; HUMANS; LEUCINE ZIPPERS; MALE; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; MOLECULAR SEQUENCE DATA; PHENOTYPE; POLYMERASE CHAIN REACTION; RADIATION HYBRID MAPPING; RIBONUCLEASE, PANCREATIC; TUMOR CELLS, CULTURED; WAGR SYNDROME;

ANIMALIA;

EID: 0037406561     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00335-002-2248-6     Document Type: Article

References (20)

1. Collavin L, Buzzai M, Saccone S, Bernard L, Federico C et al. (1998) cDNA characterization and chromosome mapping of human GAS2 gene. Genomics 48, 265-269
2. Culiat CT, Stubbs L, Nicholls RD, Montgomery CS, Russell LB et al. (1993) Concordance between isolated cleft palate in mice and alterations at the gene encoding the β3 subunit of γ-aminobutyric acid receptor. Proc Natl Acad Sci USA 90, 5105-5109
3. Fantes JA, Oghene K, Boyle S, Danes S, Fletcher JM et al. (1995) A high-resolution integrated physical, cytogenetic, and genetic map of human chromosome 11: Distal p13 to proximal p15.1. Genomics 25, 447-461
4. Friedrich G, Soriano P (1991) Promoter traps in embryonic stem cells: a genetic screen to identify and mutate developmental genes in mice. Genes Dev 5, 1513-1523
5. Gessler M, Thomas GH, Couillin P, Junien C, McGillivray BC et al. (1989) A deletion map of the WAGR region on chromosome 11. Am J Hum Genet 44, 486-495
6. Glaser T, Jepeal L, Edwards JG, Young SR, Favor J et al. (1994) PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects. Nat Genet 7, 463-471
7. Hanson IM, Seawright A, van Heyningen V (1992) The human BDNF gene maps between FSHB and HVBS1 at the boundary of 11p13-p14. Genomics 13, 1331-1333
8. Ji Y, Walkowicz MJ, Buiting K, Johnson DK, Tarvin RE et al. (1999) The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities. Hum Mol Genet 8, 533-542
9. Johnson DK, Hand RE Jr, Rinchik EM (1989) Molecular mapping within the mouse albino-deletion complex. Proc Natl Acad Sci USA 86, 8862-8866
10. Johnson DK, Stubbs LJ, Culiat CT, Montgomery CS, Russell LB et al. (1995) Molecular analysis of 36 mutations at the mouse pink-eyed dilution (p) locus. Genetics 141, 1563-1571
11. Jordan T, Hanson I, Zaletayev D, Hodgson S, Prosser J et al. (1992) The human PAX6 gene is mutated in two patients with aniridia. Nat Genet 1, 328-332
12. Leibrock J, Lottspeich F, Hohn A, Hofer M, Hengerer B et al. (1989) Molecular cloning and expression of brain-derived neurotrophic factor. Nature 341, 149-152
13. Rinchik EM, Russell LB (1990) Germ-line deletion mutations in the mouse: tools for intensive functional and physical mapping of regions of the mammalian genome. In Genome Analysis, Volume 1: Genetic and Physical Mapping, eds. K Davies, S Tilghman
14. Rinchik EM, Carpenter DA, Johnson DK (2002) Functional annotation of mammalian genomic DNA sequence by chemical mutagenesis: a fine-structure genetic mutation map of a 1- to 2-cM segment of mouse chromosome 7 corresponding to human chromosome 11p14-p15. Proc Natl Acad Sci USA 99, 844-849
15. Russell LB, Montgomery CS, Cacheiro NLA, Johnson DK (1995) Complementation analyses for 45 mutations encompassing the pink-eyed dilution (p) locus of the mouse. Genetics 141, 1547-1562
16. Russell LJ, Weisskopf B (1986) Cognition in aniridia-Wilms tumor association: analysis of karyotype association. Am J Hum Genet 39, A78
17. Russell WL (1951) X-ray induced mutations in mice. Cold Spring Harbor Symp Quant Biol 16, 327-336
18. Stubbs L, Rinchik EM, Goldberg E, Rudy B, Handel MA et al. (1994) Clustering of six human 11p15 gene homologs within a 500 kb interval of proximal mouse chromosome 7. Genomics 24, 324-332
19. Turleau C, Grouchy JD, Tournade MF, Gagnadoux MF, Junien C (1984) Del 11p/aniridia complex: report of three patients and review of 37 observations from the literature. Clin Genet 26, 356-362
20. Wu M, Rinchik EM, Johnson DK (2000) An integrated deletion and physical map encompassing 171R1, a chromosome 7 locus required for peri-implantation survival in the mouse. Genomics 67, 228-231