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          <dc:title xml:lang="en">Characterization of chromosomal damage accumulated in freeze-dried mouse spermatozoa preserved under ambient and heat stress conditions</dc:title>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="ja">日下部, 博一</jpcoar:creatorName>
            <jpcoar:creatorName xml:lang="ja-Kana">クサカベ, ヒロカズ</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="ja">立野, 裕幸</jpcoar:creatorName>
            <jpcoar:creatorName xml:lang="ja-Kana">タテノ, ヒロユキ</jpcoar:creatorName>
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          <datacite:description descriptionType="Other">http://www.ncbi.nlm.nih.gov/pubmed/21367815 | http://www.ncbi.nlm.nih.gov/pubmed/21367815</datacite:description>
          <datacite:description xml:lang="en" descriptionType="Abstract">Structural chromosome aberrations and DNA damage generated in freeze-dried mouse spermatozoa were investigated. Freeze-dried sperm samples were preserved at 4, 25 and 50℃ for short duration (1 day to 2 months) and at 25℃ for long duration (2 years). The spermatozoa were injected into mouse oocytes to analyse the chromosomes of the zygotes at the first cleavage metaphase. Chromosome break of the chromosome-type aberrations was the most common type of structural chromosome aberrations observed in all freeze-dried samples. The frequency of chromatid exchanges rapidly increased in freeze-dried spermatozoa preserved at 50℃ for 1-5 days. The frequency of chromatid-type aberrations (break and exchange) gradually increased in freeze-dried spermatozoa preserved at 25℃ for up to 2 months. Alkaline comet assay revealed significant migration of damaged DNA accumulated in freeze-dried spermatozoa preserved at 50℃ for 3 days and 25℃ for 2 years. However, no DNA damage was detected using the same sperm samples by neutral comet assay, which can detect mostly DNA double-strand breaks in cellular DNA. These results suggest that DNA single-strand breaks were accumulated in freeze-dried spermatozoa preserved under ambient or heat conditions, and then chromatid-type aberrations, especially the chromatid exchanges, were formed via post-replication repair system in zygotes.</datacite:description>
          <datacite:description descriptionType="Other">This is a pre-copy-editing, author-produced PDF of an article accepted for publication in Mutagenesis following peer review. The definitive publisher-authenticated version Kusakabe, Hirokazu ; Tateno, Hiroyuki, Mutagenesis, 26(3), 447-453. is available online at: http://mutage.oxfordjournals.org/content/26/3/447.</datacite:description>
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          <datacite:date dateType="Issued">2011-05-01</datacite:date>
          <dc:language>eng</dc:language>
          <dc:type>journal article</dc:type>
          <oaire:version>AM</oaire:version>
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            <jpcoar:relatedIdentifier identifierType="DOI">10.1093/mutage/ger003</jpcoar:relatedIdentifier>
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          <jpcoar:sourceIdentifier identifierType="PISSN">0267-8357</jpcoar:sourceIdentifier>
          <jpcoar:sourceTitle>Mutagenesis</jpcoar:sourceTitle>
          <jpcoar:volume>26</jpcoar:volume>
          <jpcoar:issue>3</jpcoar:issue>
          <jpcoar:pageStart>447</jpcoar:pageStart>
          <jpcoar:pageEnd>453</jpcoar:pageEnd>
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            <datacite:date dateType="Available">2021-07-06</datacite:date>
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