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      KCI등재 SCOPUS SCIE

      Ground-State Conditions Promote Robust Prdm14 Reactivation and Maintain an Active Dlk1-Dio3 Region during Reprogramming

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      https://www.riss.kr/link?id=A103927141

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      다국어 초록 (Multilingual Abstract)

      Induced pluripotent stem cells (iPSCs) are capable of unlimited self-renewal and can give rise to all three germ layers, thereby providing a new platform with which to study mammalian development and epigenetic reprogramming. However, iPSC generation may result in subtle epigenetic variations, such as the aberrant methylation of the Dlk1-Dio3 locus, among the clones, and this heterogeneity constitutes a major drawback to harnessing the full potential of iPSCs. Vitamin C has recently emerged as a safeguard to ensure the normal imprinting of the Dlk1-Dio3 locus during reprogramming. Here, we show that vitamin C exerts its effect in a manner that is independent of the reprogramming kinetics. Moreover, we demonstrate that reprogramming cells under 2i conditions leads to the early upregulation of Prdm14, which in turn results in a highly homogeneous population of authentic pluripotent colonies and prevents the abnormal silencing of the Dlk1-Dio3 locus.
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      Induced pluripotent stem cells (iPSCs) are capable of unlimited self-renewal and can give rise to all three germ layers, thereby providing a new platform with which to study mammalian development and epigenetic reprogramming. However, iPSC generation ...

      Induced pluripotent stem cells (iPSCs) are capable of unlimited self-renewal and can give rise to all three germ layers, thereby providing a new platform with which to study mammalian development and epigenetic reprogramming. However, iPSC generation may result in subtle epigenetic variations, such as the aberrant methylation of the Dlk1-Dio3 locus, among the clones, and this heterogeneity constitutes a major drawback to harnessing the full potential of iPSCs. Vitamin C has recently emerged as a safeguard to ensure the normal imprinting of the Dlk1-Dio3 locus during reprogramming. Here, we show that vitamin C exerts its effect in a manner that is independent of the reprogramming kinetics. Moreover, we demonstrate that reprogramming cells under 2i conditions leads to the early upregulation of Prdm14, which in turn results in a highly homogeneous population of authentic pluripotent colonies and prevents the abnormal silencing of the Dlk1-Dio3 locus.

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      참고문헌 (Reference)

      1 Esteban, M. A., "Vitamin C enhances the generation of mouse and human induced pluripotent stem cells" 6 : 71-79, 2010

      2 Saha, K., "Technical challenges in using human induced pluripotent stem cells to model disease" 5 : 584-595, 2009

      3 Buganim, Y., "Single-cell expression analyses during cellular reprogramming reveal an early stochastic and a late hierarchic phase" 150 : 1209-1222, 2012

      4 Yamaji, M., "PRDM14 ensures naive pluripotency through dual regulation of signaling and epigenetic pathways in mouse embryonic stem cells" 12 : 368-382, 2013

      5 Yamanaka, S., "Nuclear reprogramming to a pluripotent state by three approaches" 465 : 704-712, 2010

      6 Leitch, H. G., "Naive pluripotency is associated with global DNA hypomethylation" 20 : 311-316, 2013

      7 Chen, J., "H3K9 methylation is a barrier during somatic cell reprogramming into iPSCs" 45 : 34-42, 2013

      8 Sung-Hwan Moon, "Gene Expression Profiles in CHA3 and CHA4 Human Embryonic Stem Cells and Embryoid Bodies" 한국분자세포생물학회 31 (31): 315-326, 2011

      9 Chen, G., "Chemically defined conditions for human iPSC derivation and culture" 8 : 424-429, 2011

      10 Stadtfeld, M., "Ascorbic acid prevents loss of Dlk1-Dio3 imprinting and facilitates generation of all-iPS cell mice from terminally differentiated B cells" 44 : 398-S392, 2012

      1 Esteban, M. A., "Vitamin C enhances the generation of mouse and human induced pluripotent stem cells" 6 : 71-79, 2010

      2 Saha, K., "Technical challenges in using human induced pluripotent stem cells to model disease" 5 : 584-595, 2009

      3 Buganim, Y., "Single-cell expression analyses during cellular reprogramming reveal an early stochastic and a late hierarchic phase" 150 : 1209-1222, 2012

      4 Yamaji, M., "PRDM14 ensures naive pluripotency through dual regulation of signaling and epigenetic pathways in mouse embryonic stem cells" 12 : 368-382, 2013

      5 Yamanaka, S., "Nuclear reprogramming to a pluripotent state by three approaches" 465 : 704-712, 2010

      6 Leitch, H. G., "Naive pluripotency is associated with global DNA hypomethylation" 20 : 311-316, 2013

      7 Chen, J., "H3K9 methylation is a barrier during somatic cell reprogramming into iPSCs" 45 : 34-42, 2013

      8 Sung-Hwan Moon, "Gene Expression Profiles in CHA3 and CHA4 Human Embryonic Stem Cells and Embryoid Bodies" 한국분자세포생물학회 31 (31): 315-326, 2011

      9 Chen, G., "Chemically defined conditions for human iPSC derivation and culture" 8 : 424-429, 2011

      10 Stadtfeld, M., "Ascorbic acid prevents loss of Dlk1-Dio3 imprinting and facilitates generation of all-iPS cell mice from terminally differentiated B cells" 44 : 398-S392, 2012

      11 Liu, L., "Activation of the imprinted Dlk1-Dio3 region correlates with pluripotency levels of mouse stem cells" 285 : 19483-19490, 2010

      12 Stadtfeld, M., "Aberrant silencing of imprinted genes on chromosome 12qF1 in mouse induced pluripotent stem cells" 465 : 175-181, 2010

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2012-11-07 학술지명변경 한글명 : 분자와 세포 -> Molecules and Cells KCI등재
      2008-01-01 평가 SCI 등재 (등재유지) KCI등재
      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2001-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1998-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 2.77 0.19 1.85
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      1.37 1.11 0.379 0.03
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