Isolation and characterization of fetal nucleated red blood cells from maternal blood as a target for single cell sequencing-based non-invasive genetic testing 3

• Material Type: 博士論文
• ISSN: 1447-0578
• Title: Isolation and characterization of fetal nucleated red blood cells from maternal blood as a target for single cell sequencing-based non-invasive genetic testing
• Volume: 20 3
• Author/Editor: 伊東, 紀子
• Author Heading: 伊東, 紀子
• Publication Date: 2021-09-01
• Publication Date (W3CDTF): 2021-09-01
• Alternative Title: 母体血中の胎児有核赤血球細胞を標的としたシングルセルシーケンスによる出生前遺伝学的検査法の開発
• Periodical title: Reproductive Medicine and Biology
• Degree grantor/type: Nagasaki University (長崎大学)
• Date Granted: 2021-09-01
• Date Granted (W3CDTF): 2021-09-01
• Dissertation Number: 甲医歯薬第1366号
• Degree Type: 博士(薬学)
• Conferring No. (Dissertation): 甲医歯薬第1366号
• Text Language Code: eng
• Subject Heading: fetal nucleated red blood cell (fNRBC); fluorescence-activated; cell sorting (FACS), non-invasive; prenatal testing (NIPT), single cell, whole genome amplification (WGA)
• Target Audience: 一般
• Note (General): Purpose: Although non-invasive prenatal testing (NIPT) based on cell-free DNA (cfDNA) in maternal plasma has been prevailing worldwide, low levels of fetal DNA fraction may lead to false-negative results. Since fetal cells in maternal blood provide a pure source of fetal genomic DNA, we aimed to establish a workflow to isolate and sequence fetal nucleated red blood cells (fNRBCs) individually as a target for NIPT.Methods: Using male-bearing pregnancy cases, we isolated fNRBCs individually from maternal blood by FACS, and obtained their genomic sequence data through PCR screening with a Y-chromosome marker and whole-genome amplification (WGA)-based whole-genome sequencing.Results: The PCR and WGA efficiencies of fNRBC candidates were consistently lower than those of control cells. Sequencing data analyses revealed that although the majority of the fNRBC candidates were confirmed to be of fetal origin, many of the WGA-based genomic libraries from fNRBCs were considered to have been amplified from a portion of genomic DNA.Conclusions: We established a workflow to isolate and sequence fNRBCs individually. However, our results demonstrated that, to make cell-based NIPT targeting fNRBCs feasible, cell isolation procedures need to be further refined such that the nuclei of fNRBCs are kept intact.; 長崎大学学位論文 学位記番号:博(医歯薬)甲第1366号 学位授与年月日:令和3年9月1日; Author: Noriko Ito, Kazuhiro Tsukamoto, Kosuke Taniguchi, Ken Takahashi, Aikou Okamoto, Hiroaki Aoki, Yuka Otera-Takahashi, Michihiro Kitagawa, Hiroko Ogata-Kawata, Hideaki Morita, Kenichiro Hata, Kazuhiko Nakabayashi; Citation: Reproductive Medicine and Biology, 20(3), pp.352-360; 2021; identifier:Nagasaki University (長崎大学), 博士(薬学) (2021-09-01); http://hdl.handle.net/10069/00040953
• DOI: info:doi/10.1002/rmb2.12392; https://doi.org/info:doi/10.1002/rmb2.12392
• Persistent ID (NDL): info:ndljp/pid/12154368; https://dl.ndl.go.jp/pid/12154368
• Collection: 障害者向け資料
• Collection (Materials For Handicapped People:1): テキストデータ
• Collection (particular): 国立国会図書館デジタルコレクション > デジタル化資料 > 博士論文; https://dl.ndl.go.jp/collections/A00014
• Acquisition Basis: 博士論文（自動収集）
• Date Accepted (W3CDTF): 2022-03-06T04:54:00+09:00
• Date Created (W3CDTF): 2022-02-10
• Format (IMT): PDF
• Access Restrictions: 国立国会図書館内限定公開
• Service for the Digitized Contents Transmission Service: 図書館・個人送信対象外
• Availability of remote photoduplication service: 可
• Related Material (URI): http://hdl.handle.net/10069/00040953
• Periodical Title (URI): http://hdl.handle.net/10069/00041250
• Data Provider (Database): 国立国会図書館 : 国立国会図書館デジタルコレクション; https://dl.ndl.go.jp