Literature DB >> 8991069

Database and software for the analysis of mutations at the lacI gene in both transgenic rodents and bacteria.

N F Cariello1, N J Gorelick.   

Abstract

The use of transgenic rodents for the study of genetic toxicology has increased dramatically in the past several years. A great deal of the recent work has employed the lacI locus in transgenic mice. In addition to the transgenic data, a substantial amount of information exists regarding mutation of the lacI gene in bacteria. In an effort to centralize the information regarding mutations in the lacI gene in both rodents and bacteria, we have created a computerized database that contains information about DNA sequence alterations on about 500 mutations in transgenic rodents and 8,000 mutations in bacteria. We have also produced a software package for the analysis of the lacI database. Routines have been developed for the analysis of single base substitutions, including programs to (i) determine if two mutational spectra are different; (ii) determine if mutations show a DNA strand bias; (iii) determine the frequency of transitions and transversions; (iv) display the number and kind of mutations observed at each base in the coding region; (v) perform nearest neighbor analysis; and (vi) display mutable amino acids in the lacI protein. The software runs only on IBM-compatible machines running Microsoft Windows. The software and lacI database are freely available via the internet (http:/(/)sunsite.unc.edu/dnam/mainpage.++ +html).

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Year:  1996        PMID: 8991069     DOI: 10.1002/(SICI)1098-2280(1996)28:4<397::AID-EM14>3.0.CO;2-A

Source DB:  PubMed          Journal:  Environ Mol Mutagen        ISSN: 0893-6692            Impact factor:   3.216


  2 in total

1.  Databases and software for the analysis of mutations in the human p53 gene, human hprt gene and both the lacI and lacZ gene in transgenic rodents.

Authors:  N F Cariello; G R Douglas; N J Gorelick; D W Hart; J D Wilson; T Soussi
Journal:  Nucleic Acids Res       Date:  1998-01-01       Impact factor: 16.971

2.  p27kip1 deficiency impairs G2/M arrest in response to DNA damage, leading to an increase in genetic instability.

Authors:  Shannon R Payne; Shulin Zhang; Karen Tsuchiya; Russell Moser; Kay E Gurley; Gary Longton; Johan deBoer; Christopher J Kemp
Journal:  Mol Cell Biol       Date:  2007-10-22       Impact factor: 4.272

  2 in total

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