Overexpression of dJmj differentially affects intestinal stem cells and differentiated enterocytes

Jumonji (Jmj)/Jarid2 is a DNA-binding transcriptional repressor mediated via histone methylation. Nevertheless, the well-known function of Jmj is as a scaffold for the recruitment of various complexes including Polycomb repressive complex 2 (PRC2), and required for mouse embryonic stem cell developm...

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Veröffentlicht in:Cellular signalling 2018-01, Vol.42, p.194-210
Hauptverfasser: Suong, Dang Ngoc Anh, Shimaji, Kouhei, Pyo, Jung-Hoon, Park, Joung-Sun, Yoshida, Hideki, Yoo, Mi-Ae, Yamaguchi, Masamitsu
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container_issue
container_start_page 194
container_title Cellular signalling
container_volume 42
creator Suong, Dang Ngoc Anh
Shimaji, Kouhei
Pyo, Jung-Hoon
Park, Joung-Sun
Yoshida, Hideki
Yoo, Mi-Ae
Yamaguchi, Masamitsu
description Jumonji (Jmj)/Jarid2 is a DNA-binding transcriptional repressor mediated via histone methylation. Nevertheless, the well-known function of Jmj is as a scaffold for the recruitment of various complexes including Polycomb repressive complex 2 (PRC2), and required for mouse embryonic stem cell development. However, PRC2 independent function is suggested for Drosophila Jumonji (dJmj). To clarify the function of dJmj during cell differentiation, we used Drosophila adult intestinal stem cell system that allows to follow stem cell behaviors in vivo. Overexpression of dJmj in intestinal stem cells/enteroblasts (ISCs/EBs) induces cell-autonomous ISC proliferation followed by differentiation, that is controlled by the Notch and EGFR pathway. In contrast, overexpression of dJmj in enterocytes (ECs) resulted in activation of the JNK pathway in ECs followed by the induction of apoptosis. Activated JNK increased the level of Yorkie in ECs and induced the reduction of Upd proteins and EGFR ligands, which activated the JAK/STAT and EGFR pathway in both ISCs and EBs to promote ISC proliferation. The Notch signaling pathway appears to be highly activated to support the differentiation of EBs to ECs. Thus, the combination of these signaling pathways caused by ECs-specific dJmj-overexpression induced non-cell-autonomous ISC proliferation and differentiation. Surprisingly, these effects did not relate to H3K27me3 status, likely represented PRC2 activity, in cells that overexpressed dJmj. Instead of this, the disappearance of H3K27me3 in ISC/EB-specific overexpressed dJmj suggested a possible PRC2-independent role of dJmj in regulating chromatin structure. •ISC/EB-specific dJmj-overexpression induced the cell-autonomous ISC over-proliferation.•EC-specific dJmj-overexpression triggered apoptosis in ECs followed by non-cell-autonomous ISC over-proliferation.•Effects caused by dJmj-overexpression do not relate to H3K27me3 status.•PRC2-independent role of dJmj in regulating chromatin structure during differentiation process is suggested.
doi_str_mv 10.1016/j.cellsig.2017.10.017
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Nevertheless, the well-known function of Jmj is as a scaffold for the recruitment of various complexes including Polycomb repressive complex 2 (PRC2), and required for mouse embryonic stem cell development. However, PRC2 independent function is suggested for Drosophila Jumonji (dJmj). To clarify the function of dJmj during cell differentiation, we used Drosophila adult intestinal stem cell system that allows to follow stem cell behaviors in vivo. Overexpression of dJmj in intestinal stem cells/enteroblasts (ISCs/EBs) induces cell-autonomous ISC proliferation followed by differentiation, that is controlled by the Notch and EGFR pathway. In contrast, overexpression of dJmj in enterocytes (ECs) resulted in activation of the JNK pathway in ECs followed by the induction of apoptosis. Activated JNK increased the level of Yorkie in ECs and induced the reduction of Upd proteins and EGFR ligands, which activated the JAK/STAT and EGFR pathway in both ISCs and EBs to promote ISC proliferation. The Notch signaling pathway appears to be highly activated to support the differentiation of EBs to ECs. Thus, the combination of these signaling pathways caused by ECs-specific dJmj-overexpression induced non-cell-autonomous ISC proliferation and differentiation. Surprisingly, these effects did not relate to H3K27me3 status, likely represented PRC2 activity, in cells that overexpressed dJmj. 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subjects Animals
Apoptosis - genetics
Cell Differentiation
Cell over-proliferation
Cell Proliferation
Chromatin - chemistry
Chromatin - metabolism
Drosophila intestinal stem cell
Drosophila melanogaster - genetics
Drosophila melanogaster - growth & development
Drosophila melanogaster - metabolism
Drosophila Proteins - genetics
Drosophila Proteins - metabolism
EGFR
Enterocytes - cytology
Enterocytes - metabolism
ErbB Receptors - genetics
ErbB Receptors - metabolism
Gene Expression Regulation, Developmental
Histone-Lysine N-Methyltransferase - genetics
Histone-Lysine N-Methyltransferase - metabolism
Histones - genetics
Histones - metabolism
Intestinal Mucosa - metabolism
Intestines - cytology
Intestines - growth & development
JAK/STAT
JNK
Jumonji/Jarid2
MAP Kinase Signaling System
Nuclear Proteins - genetics
Nuclear Proteins - metabolism
Receptors, Invertebrate Peptide - genetics
Receptors, Invertebrate Peptide - metabolism
Receptors, Notch - genetics
Receptors, Notch - metabolism
STAT Transcription Factors - genetics
STAT Transcription Factors - metabolism
Stem Cells - cytology
Stem Cells - metabolism
Trans-Activators - genetics
Trans-Activators - metabolism
Transcription Factors - genetics
Transcription Factors - metabolism
title Overexpression of dJmj differentially affects intestinal stem cells and differentiated enterocytes
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