TY - JOUR
T1 - Identification and expression of the cDNA of KIN17, a zinc-finger gene located on mouse chromosome 2, encoding a new DNA-binding protein
AU - Angulo, Jaime F.
AU - Rouer, Evelyne
AU - Mazin, Alexander
AU - Mattei, Marie geneviève
AU - Tissier, Agnèves
AU - Horellou, Philippe
AU - Benarous, Richard
AU - Devoret, Raymond
N1 - Funding Information:
We are grateful to M.Pierre and N.Roeckel for their expert assistance, and to M.Coignet and S.Lavareda de Souza for their help. H.Okayama is thanked for providing the mouse pcD2 library and R.Bertolotti, J.L.Danan, J.Mallet, J.P.Waller for their discussions and advice. J.A. and A.M. are grateful to G.de Murcia and J.Menissier for advice and hospitality in their laboratory. J.Angulo and A.Mazin benefited from fellowships from the Association pour la Recherche sur le Cancer and the Centre National de la Recherche Scientifique, and from the International Agency on Research against Cancer. Grants from the European Community (BI6-E-145-F), the Institut National de la Sant^ et de la Recherche M6dicale, the Association pour la Recherche sur le Cancer no. 6093 and 6342, the Fondation pour la Recherche Meclicale, and the Ligue Francaise contre le Cancer provided invaluable support.
PY - 1991/10/11
Y1 - 1991/10/11
N2 - We report the cloning of KIN17 cDNA, 1414 bp long with an ORF of 391 residues showing a zinc finger and nuclear localization signals. By recloning the cDNA into an appropriate vector, we produced kln17 protein in E.coli, purified it partially and shown that kin17 protein binds to double-stranded DNA. The KIN 17 gene was localized by cytogenetic mapping in mouse chromosome 2, band A. Genomic sequences homologous to KIN17 cDNA were detected also in rat and human DNAs. KIN17 mRNA is highly expressed in rodent transformed AtT-20 neuroendocrine cells whereas it can be detected only in the total RNA of mouse embryos and various normal adult tissues by reverse transcription and PCR amplification. The mouse nuclear kin17 protein was identified by a local small structural similarity with E.coli recA protein. Kin17 and recA have only 39 amino acid residues in a region that might be involved in DNA-binding.
AB - We report the cloning of KIN17 cDNA, 1414 bp long with an ORF of 391 residues showing a zinc finger and nuclear localization signals. By recloning the cDNA into an appropriate vector, we produced kln17 protein in E.coli, purified it partially and shown that kin17 protein binds to double-stranded DNA. The KIN 17 gene was localized by cytogenetic mapping in mouse chromosome 2, band A. Genomic sequences homologous to KIN17 cDNA were detected also in rat and human DNAs. KIN17 mRNA is highly expressed in rodent transformed AtT-20 neuroendocrine cells whereas it can be detected only in the total RNA of mouse embryos and various normal adult tissues by reverse transcription and PCR amplification. The mouse nuclear kin17 protein was identified by a local small structural similarity with E.coli recA protein. Kin17 and recA have only 39 amino acid residues in a region that might be involved in DNA-binding.
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U2 - 10.1093/nar/19.19.5117
DO - 10.1093/nar/19.19.5117
M3 - Article
C2 - 1923796
AN - SCOPUS:0025993155
SN - 0305-1048
VL - 19
SP - 5117
EP - 5123
JO - Nucleic acids research
JF - Nucleic acids research
IS - 19
ER -