Skip to main content
Log in

Mapping of the mouse bilirubin UDP-glucuronosyltransferase gene (Gnt-1) to chromosome 1 by restriction fragment length variations

  • Published:
Biochemical Genetics Aims and scope Submit manuscript

Abstract

Restriction endonuclease fragment length variations (RFLVs) were detected by using a rat cDNA probe for the bilirubin UDP-glucuronosyltransferase (UDPGT) gene between two mouse strains, 129/Sv and MOL-MIT. RFLVs of the gene were found byEcoRI andPvuII digestions. From linkage analyses of the three-point cross test usingElo andEn-1 as marker genes, the bilirubin UDPGT gene was mapped at position 37 on chromosome 1. Bilirubin and phenol UDPGTs have been suggested to be expressed by a single gene by alternative splicing in human and rat. The mouse bilirubin UDPGT gene was namedGnt-1.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Arias, I. M., Gartner, L. M., Cohen, M., Ezzer, J., and Levi, A. J. (1969). Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency.Am. J. Med. 47395.

    Google Scholar 

  • Harding, D., Jeremiah, S. J., Povey, S., and Burchell, B. (1990). Chromosomal mapping of a human phenol UDP-glucuronosyltransferase,GNT-1.Ann. Hum. Genet. 5417.

    Google Scholar 

  • Hill, R. E., Hall, A. E., Sime, C. M., and Hastie, N. D. (1987). A mouse homeo box-containing gene maps near a developmental mutation.Cytogenet. Cell Genet. 44171.

    Google Scholar 

  • Iyanagi, T., and Emi, Y. (1991). Molecular basis of multiple UDP-glucuronosyltransferase isoenzyme deficiencies in the hyper-bilirubinemic rat (Gunn rat).Seikagaku 63753 (abstr. in Japanese).

    Google Scholar 

  • Lathe, G. H., and Walker, M. (1958). The synthesis of bilirubin glucuronide in animal and human liver.Biochem. J. 70705.

    Google Scholar 

  • Lyon, M. F., and Kirby, M. C. (1991). Mouse chromosome atlas.Mouse News Lett. 8938.

    Google Scholar 

  • Nagai, F., Homma, H., Tanase, H., and Matsui, M. (1988). Studies on the genetic linkage of bilirubin and androsterone UDP-glucuronyltransferases by cross-breeding of two mutant rat strains.Biochem. J. 252897.

    Google Scholar 

  • Oda, S., Watanabe, T., and Kondo, K. (1980). A new mutation, eye lens obsolescence,Elo on chromosome 1 in the mouse.Jap. J. Genet. 5571.

    Google Scholar 

  • Rigby, P. W., Dieckmann, M., Rhodes, C., and Berg, P. (1977). Labeling deoxyribonucleic acid to high specific activityin vitro by nick-translation with DNA polymerase I.J. Mol. Biol. 113237.

    Google Scholar 

  • Ritter, J. K., Crawford, J. M., and Owens, I. S. (1991). Cloning of two human liver bilirubin UDP-glucuronosyltransferase cDNAs with expression in COS-1 cells.J. Biol. Chem. 2661043.

    Google Scholar 

  • Sato, H., Koiwai, O., Tanabe, K., and Kashiwamata, S. (1990). Isolation and sequencing of rat liver bilirubin UDP-glucuronosyltransferase cDNA: Possible alternate splicing of a common primary transcript.Biochem. Biophys. Res. Commun. 169260.

    Google Scholar 

  • Sato, H., Aono, S., Kashiwamata, S., and Koiwai, O. (1991). Genetic defect of bilirubin UDP-glucuronosyltransferase in the hyperbilirubinemic Gunn rat.Biochem. Biophys. Res. Commun. 1771161.

    Google Scholar 

  • Schmid, R., and Hammaker, L. (1963). Metabolism and disposition of14C-bilirubin in congenital nonhemolytic jaundice.J. Clin. Invest. 421720.

    Google Scholar 

  • Scragg, L., Celier, C., and Burchell, B. (1985). Congenital jaundice in rats due to the absence of hepatic bilirubin UDP-glucuronyltransferase enzyme protein.FEBS Lett. 18337.

    Google Scholar 

  • Southern, E. M. (1975). Detection of specific sequences among DNA fragments separated by gel electrophoresis.J. Mol. Biol. 98503.

    Google Scholar 

  • Wahl, G. M., Stern, M., and Stark, G. R. (1979). Efficient transfer of large DNA fragments from agarose gels to diazobenzyloxymethyl-paper and rapid hybridization by using dextran sulfate.Proc. Natl. Acad. Sci. USA 763683.

    Google Scholar 

  • Watanabe, T., Shimizu, A., Ohno, K., Masaki, S., and Kondo, K. (1989). Restriction fragment length variations and chromosomal mapping of two mouse metallothionein genes,Mt-1 andMt-2.Biochem. Genet. 27689.

    Google Scholar 

  • Watanabe, T., Sakai, Y., Miyawaki, S., Shimizu, A., Koiwai, O., and Ohno, K. (1991). A molecular genetic linkage map of mouse chromosome 19, includinglpr, Ly-44, andTdt genes.Biochem. Genet. 29325.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

This study was supported by Grant-in-Aid for Research Project A-II from the Institute for Developmental Research, Aichi Prefecture Colony.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sato, H., Sakai, Y., Koiwai, O. et al. Mapping of the mouse bilirubin UDP-glucuronosyltransferase gene (Gnt-1) to chromosome 1 by restriction fragment length variations. Biochem Genet 30, 347–352 (1992). https://doi.org/10.1007/BF00569325

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00569325

Key words

Navigation