Integrative analysis of single-cell RNA-seq and ATAC-seq reveals heterogeneity of induced pluripotent stem cell-derived hepatic organoids

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dc.contributor.authorJong-Hwan Kim-
dc.contributor.authorSeon Ju Mun-
dc.contributor.authorJeong Hwan Kim-
dc.contributor.authorMyung Jin Son-
dc.contributor.authorSeon-Young Kim-
dc.date.accessioned2023-09-11T16:32:48Z-
dc.date.available2023-09-11T16:32:48Z-
dc.date.issued2023-
dc.identifier.issn2589-0042-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/32715-
dc.description.abstractTo gain deeper insights into transcriptomes and epigenomes of organoids, liver organoids from two states (expandable and more differentiated) were subjected to single-cell RNA-seq (scRNA-seq) and single-cell ATAC-seq (scATAC-seq) analyses. Mitochondrial gene expression was higher in differentiated than in non-differentiated hepatocytes, with ATAC-seq peaks increasing near the mitochondrial control region. Differentiation of liver organoids resulted in the expression of transcription factors that act as enhancers and repressors. In addition, epigenetic mechanisms regulating the expression of alpha-fetoprotein (AFP) and albumin (ALB) differed in liver organoids and adult liver. Knockdown of PDX1, an essential transcription factor for pancreas development, led to the hepatic maturation of liver organoids through regulation of AFP and ALB expression. This integrative analysis of the transcriptomes and epigenomes of liver organoids at the single-cell level may contribute to a better understanding of the regulatory networks during liver development and the further development of mature in vitro human liver models.-
dc.publisherElsevier-Cell Press-
dc.titleIntegrative analysis of single-cell RNA-seq and ATAC-seq reveals heterogeneity of induced pluripotent stem cell-derived hepatic organoids-
dc.title.alternativeIntegrative analysis of single-cell RNA-seq and ATAC-seq reveals heterogeneity of induced pluripotent stem cell-derived hepatic organoids-
dc.typeArticle-
dc.citation.titleiScience-
dc.citation.number9-
dc.citation.endPage107675-
dc.citation.startPage107675-
dc.citation.volume26-
dc.contributor.affiliatedAuthorJong-Hwan Kim-
dc.contributor.affiliatedAuthorSeon Ju Mun-
dc.contributor.affiliatedAuthorJeong Hwan Kim-
dc.contributor.affiliatedAuthorMyung Jin Son-
dc.contributor.affiliatedAuthorSeon-Young Kim-
dc.contributor.alternativeName김종환-
dc.contributor.alternativeName문선주-
dc.contributor.alternativeName김정환-
dc.contributor.alternativeName손명진-
dc.contributor.alternativeName김선영-
dc.identifier.bibliographicCitationiScience, vol. 26, no. 9, pp. 107675-107675-
dc.identifier.doi10.1016/j.isci.2023.107675-
dc.description.journalClassY-
Appears in Collections:
Aging Convergence Research Center > 1. Journal Articles
Division of Research on National Challenges > Stem Cell Convergenece Research Center > 1. Journal Articles
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