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・ Deoxyguanosine diphosphate
・ Deoxyguanosine kinase
・ Deoxyguanosine monophosphate
・ Deoxyguanosine triphosphate
・ Deoxyhypusine monooxygenase
・ Deoxyhypusine synthase
・ Deoxyinosine monophosphate
・ Deoxylimonate A-ring-lactonase
・ Deoxynucleoside kinase
・ Deoxynucleotide 3'-phosphatase
・ Deoxypyridinoline
・ Deoxyribodipyrimidine endonucleosidase
・ Deoxyribodipyrimidine photo-lyase
・ Deoxyribonuclease
・ Deoxyribonuclease (pyrimidine dimer)
Deoxyribonuclease I
・ Deoxyribonuclease II
・ Deoxyribonuclease IV
・ Deoxyribonuclease V
・ Deoxyribonuclease X
・ Deoxyribonucleoprotein
・ Deoxyribonucleoside
・ Deoxyribonucleotide
・ Deoxyribose
・ Deoxyribose-phosphate aldolase
・ Deoxyribozyme
・ Deoxys
・ Deoxysarpagine hydroxylase
・ Deoxyschizandrin
・ Deoxyuridine


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Deoxyribonuclease I : ウィキペディア英語版
Deoxyribonuclease I

Deoxyribonuclease I (usually called DNase I), is an endonuclease coded by the human gene DNASE1.〔(【引用サイトリンク】 url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=1773 )
DNase I is a nuclease that cleaves DNA preferentially at phosphodiester linkages adjacent to a pyrimidine nucleotide, yielding 5'-phosphate-terminated polynucleotides with a free hydroxyl group on position 3', on average producing tetranucleotides. It acts on single-stranded DNA, double-stranded DNA, and chromatin. In addition to its role as a waste-management endonuclease, it has been suggested to be one of the deoxyribonucleases responsible for DNA fragmentation during apoptosis.
DNase I binds to the cytoskeletal protein actin. It binds actin monomers with very high (sub-nanomolar) affinity and actin polymers with lower affinity. The function of this interaction is unclear. However, since actin-bound DNase I is enzymatically inactive, the DNase-actin complex might be a storage form of DNase I that prevents damage of the genetic information.

__NOTOC__
==In genomics==
In genomics, DNase I hypersensitive sites are thought to be characterized by open, accessible chromatin; therefore, a DNase I sensitivity assay is a widely used methodology in genomics for identifying which regions of the genome are likely to contain active genes

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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