Literature DB >> 20967767

Global analysis of single nucleotide polymorphisms in the exons of human deoxyribonuclease I-like 1 and 2 genes.

Junko Fujihara1, Toshihiro Yasuda, Reiko Iida, Kaori Kimura-Kataoka, Mikiko Soejima, Yoshiro Koda, Hideaki Kato, Arturo Panduro, Isao Yuasa, Haruo Takeshita.   

Abstract

Several SNPs in the deoxyribonuclease I-like 1 (DNase 1L1) and DNase 1L2 were investigated. In the present study, the genotype distributions of three synonymous SNPs (V59V, rs1050095; P67P, rs1130929; A277A, rs17849495) in the DNase 1L1 gene and four non-synonymous SNPs, V122I (rs34952165), Q170H (rs6643670), and D227A (rs5987256) in the DNase 1L1 gene, as well as D197A (rs62621282) in the DNase 1L2 gene were investigated in 13 populations. In all the populations, no variation was found in four SNPs (V59V, Q170H, D227A, and A277A) in DNASE1L1 or in D197A in DNASE1L2. As for V122I, only the German population showed a low degree of polymorphism. The SNP V122I in DNASE1L1 was monoallelic for the G-allele in all of the Asian and African populations examined, with no polymorphism being evident. Since the A-allele in SNP V122I was distributed in only the Caucasian populations, not in the other ethnic groups, it was confirmed that the A-allele in SNP V122I was Caucasian-specific. On the other hand, only P67P in DNASE1L1 was polymorphic among three synonymous SNPs. The effect of nucleotide substitution corresponding to polymorphic SNP P67P on DNase 1L1 activity was examined: the corresponding nucleotide substitution in polymorphic SNP P67P has little effect on the DNase activity.

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Year:  2010        PMID: 20967767     DOI: 10.1002/elps.201000319

Source DB:  PubMed          Journal:  Electrophoresis        ISSN: 0173-0835            Impact factor:   3.535


  3 in total

1.  Evaluation of all nonsynonymous single-nucleotide polymorphisms in the gene encoding human deoxyribonuclease I-like 1, possibly implicated in the blocking of endocytosis-mediated foreign gene transfer.

Authors:  Misuzu Ueki; Kaori Kimura-Kataoka; Junko Fujihara; Haruo Takeshita; Reiko Iida; Toshihiro Yasuda
Journal:  DNA Cell Biol       Date:  2013-12-13       Impact factor: 3.311

2.  In situ labeling of DNA reveals interindividual variation in nuclear DNA breakdown in hair and may be useful to predict success of forensic genotyping of hair.

Authors:  Sandra Szabo; Karin Jaeger; Heinz Fischer; Erwin Tschachler; Walther Parson; Leopold Eckhart
Journal:  Int J Legal Med       Date:  2011-04-08       Impact factor: 2.686

3.  Survey of single-nucleotide polymorphisms in the gene encoding human deoxyribonuclease I-like 2 producing loss of function potentially implicated in the pathogenesis of parakeratosis.

Authors:  Misuzu Ueki; Haruo Takeshita; Natsuko Utsunomiya; Takanao Chino; Noritaka Oyama; Minoru Hasegawa; Kaori Kimura-Kataoka; Junko Fujihara; Reiko Iida; Toshihiro Yasuda
Journal:  PLoS One       Date:  2017-04-10       Impact factor: 3.240

  3 in total

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