Genome organization and polymorphism of the murine beta-glucuronidase region.

Citation data:

Page: 25-31

Publication Year:
1988

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Repository URL:
https://mouseion.jax.org/stfb1980_1989/1046
Author(s):
Moore, K J; Paigen, K
Tags:
Cloning-Molecular; Comparative-Study; DNA-Restriction-Enzymes; Genes-Structural; Glucuronidase: ge; Haplotypes; Mice; Mice-Inbred-C57BL; Polymorphism-(Genetics); SUPPORT-U-S-GOVT-P-H-S
article description
Thirty-eight kilobases of mouse genomic DNA which surround and include the coding sequences for beta-glucuronidase has been mapped. Intron-exon arrangements were determined by hybridization of genomic sequences with cDNA clones, and minimum estimates of gene length (11-17 kb) and intron number were obtained. Only a single gene was observed when genomic DNA was probed with subclones containing beta-glucuronidase coding sequence; there was no evidence of duplicated or pseudogenes. However, sequences distal to the 3' end of the gene are present elsewhere in the genome in a limited number of copies. Eight haplotypes of the beta-glucuronidase region with differing regulatory genotypes were compared for restriction fragment polymorphisms. Surprisingly little was found, considering the diverse origin of the haplotypes. Two of the polymorphisms that were found may be correlated with regulatory phenotypes. A BamHI site is missing from the CS and CL haplotypes that share regulatory properties, and a 0.2-kb insertion is consistently present in haplotypes showing increased response to induction by androgens in kidney.