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GATA4 negatively regulates osteoblast differentiation by downregulation of Runx2
Osteoblasts are specialized mesenchymal cells that areresponsible for bone formation. In this study, we examine therole of GATA4 in osteoblast differentiation. GATA4 wasabundantly expressed in preosteoblast cells and graduallydown-regulated during osteoblast differentiation. Overexpressionof GATA4 i...
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Published in: | BMB reports 2014-08, Vol.47 (8), p.463-468 |
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creator | Song, Insun Kim, Kabsun Kim, Jung Ha Lee, Young-Kyoung Jung, Hyun-Jung Byun, Hae-Ok Yoon, Gyesoon Kim, Nacksung |
description | Osteoblasts are specialized mesenchymal cells that areresponsible for bone formation. In this study, we examine therole of GATA4 in osteoblast differentiation. GATA4 wasabundantly expressed in preosteoblast cells and graduallydown-regulated during osteoblast differentiation. Overexpressionof GATA4 in osteoblastic cells inhibited alkalinephosphatase activity and nodule formation in osteogenicconditioned cell culture system. In addition, overexpressionof GATA4 attenuated expression of osteogenic marker genes, including Runx2, alkaline phosphatase, bone sialoprotein, and osteocalcin, all of which are important for osteoblastdifferentiation and function. Overexpression of GATA4attenuated Runx2 promoter activity, whereas silencing ofGATA4 increased Runx2 induction. We found that GATA4interacted with Dlx5 and subsequently decreased Dlx5binding activity to Runx2 promoter region. Our data suggestthat GATA4 acts as a negative regulator in osteoblastdifferentiation by downregulation of Runx2. |
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In this study, we examine therole of GATA4 in osteoblast differentiation. GATA4 wasabundantly expressed in preosteoblast cells and graduallydown-regulated during osteoblast differentiation. Overexpressionof GATA4 in osteoblastic cells inhibited alkalinephosphatase activity and nodule formation in osteogenicconditioned cell culture system. In addition, overexpressionof GATA4 attenuated expression of osteogenic marker genes, including Runx2, alkaline phosphatase, bone sialoprotein, and osteocalcin, all of which are important for osteoblastdifferentiation and function. Overexpression of GATA4attenuated Runx2 promoter activity, whereas silencing ofGATA4 increased Runx2 induction. We found that GATA4interacted with Dlx5 and subsequently decreased Dlx5binding activity to Runx2 promoter region. Our data suggestthat GATA4 acts as a negative regulator in osteoblastdifferentiation by downregulation of Runx2.</description><identifier>ISSN: 1976-6696</identifier><identifier>EISSN: 1976-670X</identifier><language>kor</language><publisher>생화학분자생물학회</publisher><subject>Dlx5 ; GATA4 ; Osteoblast differentiation ; Runx2 ; Transcription factor</subject><ispartof>BMB reports, 2014-08, Vol.47 (8), p.463-468</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881</link.rule.ids></links><search><creatorcontrib>Song, Insun</creatorcontrib><creatorcontrib>Kim, Kabsun</creatorcontrib><creatorcontrib>Kim, Jung Ha</creatorcontrib><creatorcontrib>Lee, Young-Kyoung</creatorcontrib><creatorcontrib>Jung, Hyun-Jung</creatorcontrib><creatorcontrib>Byun, Hae-Ok</creatorcontrib><creatorcontrib>Yoon, Gyesoon</creatorcontrib><creatorcontrib>Kim, Nacksung</creatorcontrib><title>GATA4 negatively regulates osteoblast differentiation by downregulation of Runx2</title><title>BMB reports</title><addtitle>BMB Reports</addtitle><description>Osteoblasts are specialized mesenchymal cells that areresponsible for bone formation. 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Our data suggestthat GATA4 acts as a negative regulator in osteoblastdifferentiation by downregulation of Runx2.</description><subject>Dlx5</subject><subject>GATA4</subject><subject>Osteoblast differentiation</subject><subject>Runx2</subject><subject>Transcription factor</subject><issn>1976-6696</issn><issn>1976-670X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNo9zk9LwzAYBvAgCo65T-AlF4-F5G3-NMcydOoGk9HDbiUxyQirqTSZ2m9vxenpfXj48fBeoBlVUhRCkv3lXxZKXKNFSsEQxmRJpSIz9LKqm5rh6A46hw_XjXhwh1Ons0u4T9n1ptMpYxu8d4OLOUysj9iM2Paf8Wx_mt7j3Sl-wQ268rpLbnG-c9Q83DfLx2KzXT0t601x5EQWUgMlkhlwTBnFmNW28iVVjBhKrLAeptc5SM65VdrRKUleUWUBLFWvVTlHd7-zx5ByaKNNXftcr7dAKANBuKJEUC4nd_vvUvs-hDc9jG0JYhJQfgPIk1Po</recordid><startdate>20140830</startdate><enddate>20140830</enddate><creator>Song, Insun</creator><creator>Kim, Kabsun</creator><creator>Kim, Jung Ha</creator><creator>Lee, Young-Kyoung</creator><creator>Jung, Hyun-Jung</creator><creator>Byun, Hae-Ok</creator><creator>Yoon, Gyesoon</creator><creator>Kim, Nacksung</creator><general>생화학분자생물학회</general><scope>HZB</scope><scope>Q5X</scope><scope>JDI</scope></search><sort><creationdate>20140830</creationdate><title>GATA4 negatively regulates osteoblast differentiation by downregulation of Runx2</title><author>Song, Insun ; Kim, Kabsun ; Kim, Jung Ha ; Lee, Young-Kyoung ; Jung, Hyun-Jung ; Byun, Hae-Ok ; Yoon, Gyesoon ; Kim, Nacksung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-k507-7a21074b2e49b944dad8f31940b10d6df2670527555d9ae127575819d22d19c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>2014</creationdate><topic>Dlx5</topic><topic>GATA4</topic><topic>Osteoblast differentiation</topic><topic>Runx2</topic><topic>Transcription factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Song, Insun</creatorcontrib><creatorcontrib>Kim, Kabsun</creatorcontrib><creatorcontrib>Kim, Jung Ha</creatorcontrib><creatorcontrib>Lee, Young-Kyoung</creatorcontrib><creatorcontrib>Jung, Hyun-Jung</creatorcontrib><creatorcontrib>Byun, Hae-Ok</creatorcontrib><creatorcontrib>Yoon, Gyesoon</creatorcontrib><creatorcontrib>Kim, Nacksung</creatorcontrib><collection>Korean Studies Information Service System (KISS)</collection><collection>Korean Studies Information Service System (KISS) B-Type</collection><collection>KoreaScience</collection><jtitle>BMB reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Song, Insun</au><au>Kim, Kabsun</au><au>Kim, Jung Ha</au><au>Lee, Young-Kyoung</au><au>Jung, Hyun-Jung</au><au>Byun, Hae-Ok</au><au>Yoon, Gyesoon</au><au>Kim, Nacksung</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>GATA4 negatively regulates osteoblast differentiation by downregulation of Runx2</atitle><jtitle>BMB reports</jtitle><addtitle>BMB Reports</addtitle><date>2014-08-30</date><risdate>2014</risdate><volume>47</volume><issue>8</issue><spage>463</spage><epage>468</epage><pages>463-468</pages><issn>1976-6696</issn><eissn>1976-670X</eissn><abstract>Osteoblasts are specialized mesenchymal cells that areresponsible for bone formation. In this study, we examine therole of GATA4 in osteoblast differentiation. GATA4 wasabundantly expressed in preosteoblast cells and graduallydown-regulated during osteoblast differentiation. Overexpressionof GATA4 in osteoblastic cells inhibited alkalinephosphatase activity and nodule formation in osteogenicconditioned cell culture system. In addition, overexpressionof GATA4 attenuated expression of osteogenic marker genes, including Runx2, alkaline phosphatase, bone sialoprotein, and osteocalcin, all of which are important for osteoblastdifferentiation and function. Overexpression of GATA4attenuated Runx2 promoter activity, whereas silencing ofGATA4 increased Runx2 induction. We found that GATA4interacted with Dlx5 and subsequently decreased Dlx5binding activity to Runx2 promoter region. 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issn | 1976-6696 1976-670X |
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source | PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Dlx5 GATA4 Osteoblast differentiation Runx2 Transcription factor |
title | GATA4 negatively regulates osteoblast differentiation by downregulation of Runx2 |
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