Expression Profiling and Functional Analysis of Candidate Col10a1 Regulators Identified by the TRAP Program

Hypertrophic chondrocytes and their specific marker, the type X collagen gene (Col10a1), are critical components of endochondral bone formation during skeletal development. We previously found that Runx2 is an indispensable mouse Col10a1 gene regulator and identified many other transcription factors...

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Main Authors: Huiqin Bian, Ting Zhu, Yuting Liang, Ruoxuan Hei, Xiaojing Zhang, Xiaochen Li, Jinnan Chen, Yaojuan Lu, Junxia Gu, Longwei Qiao, Qiping Zheng
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-07-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2021.683939/full
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record_format Article
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language English
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author Huiqin Bian
Ting Zhu
Yuting Liang
Ruoxuan Hei
Xiaojing Zhang
Xiaochen Li
Jinnan Chen
Yaojuan Lu
Yaojuan Lu
Junxia Gu
Longwei Qiao
Qiping Zheng
Qiping Zheng
spellingShingle Huiqin Bian
Ting Zhu
Yuting Liang
Ruoxuan Hei
Xiaojing Zhang
Xiaochen Li
Jinnan Chen
Yaojuan Lu
Yaojuan Lu
Junxia Gu
Longwei Qiao
Qiping Zheng
Qiping Zheng
Expression Profiling and Functional Analysis of Candidate Col10a1 Regulators Identified by the TRAP Program
Frontiers in Genetics
Col10a1 regulators
Tbx-5
Runx2
TRAP program
chondrocyte hypertrophy
skeletal disease
author_facet Huiqin Bian
Ting Zhu
Yuting Liang
Ruoxuan Hei
Xiaojing Zhang
Xiaochen Li
Jinnan Chen
Yaojuan Lu
Yaojuan Lu
Junxia Gu
Longwei Qiao
Qiping Zheng
Qiping Zheng
author_sort Huiqin Bian
title Expression Profiling and Functional Analysis of Candidate Col10a1 Regulators Identified by the TRAP Program
title_short Expression Profiling and Functional Analysis of Candidate Col10a1 Regulators Identified by the TRAP Program
title_full Expression Profiling and Functional Analysis of Candidate Col10a1 Regulators Identified by the TRAP Program
title_fullStr Expression Profiling and Functional Analysis of Candidate Col10a1 Regulators Identified by the TRAP Program
title_full_unstemmed Expression Profiling and Functional Analysis of Candidate Col10a1 Regulators Identified by the TRAP Program
title_sort expression profiling and functional analysis of candidate col10a1 regulators identified by the trap program
publisher Frontiers Media S.A.
series Frontiers in Genetics
issn 1664-8021
publishDate 2021-07-01
description Hypertrophic chondrocytes and their specific marker, the type X collagen gene (Col10a1), are critical components of endochondral bone formation during skeletal development. We previously found that Runx2 is an indispensable mouse Col10a1 gene regulator and identified many other transcription factors (TFs) that potentially interact with the 150-bp Col10a1 cis-enhancer. However, the roles of these candidate TFs in Col10a1 expression and chondrocyte hypertrophy have not been elucidated. Here, we focus on 32 candidate TFs recently identified by analyzing the 150-bp Col10a1 enhancer using the transcription factor affinity prediction (TRAP) program. We found that 12 TFs (Hoxa3, Lsx, Evx2, Dlx5, S8, Pax2, Egr2, Mef2a, Barhl2, GKlf, Sox17, and Crx) were significantly upregulated and four TFs (Lhx4, Tbx5, Mef2c, and Hb9) were significantly downregulated in hypertrophic MCT cells, which show upregulation of Col10a1 expression. Most of the differential expression pattern of these TFs conformed with the results obtained from ATDC5 cell model and primary mouse chondrocytes. Notably, Tbx5 was downregulated upon Col10a1 upregulation, overexpression of Tbx5 decreased Col10a1 expression, and knock-down of Tbx5 increased Col10a1 expression in hypertrophic chondrocytes, suggesting that Tbx5 is a negative regulator of Col10a1. We further generated a stable Tbx5-overexpressing ATDC5 cell line and ColX-Tbx5 transgenic mice driven by Col10a1-specific enhancers and promoters. Tbx5 overexpression decreased Col10a1 expression in ATDC5 cells cultured as early as day 7 and in limb tissue on post-natal day 1. Slightly weaker alkaline phosphatase staining was also observed in cell culture on day 7 and in limb digits on embryonic day 17.5, indicating mildly delayed ossification. Further characterization of these candidate Col10a1 transcriptional regulators could help identify novel therapeutic targets for skeletal diseases associated with abnormal chondrocyte hypertrophy.
topic Col10a1 regulators
Tbx-5
Runx2
TRAP program
chondrocyte hypertrophy
skeletal disease
url https://www.frontiersin.org/articles/10.3389/fgene.2021.683939/full
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spelling doaj-b1b34507dc274e6b9ba0a52d5f27e5082021-07-02T07:31:09ZengFrontiers Media S.A.Frontiers in Genetics1664-80212021-07-011210.3389/fgene.2021.683939683939Expression Profiling and Functional Analysis of Candidate Col10a1 Regulators Identified by the TRAP ProgramHuiqin Bian0Ting Zhu1Yuting Liang2Ruoxuan Hei3Xiaojing Zhang4Xiaochen Li5Jinnan Chen6Yaojuan Lu7Yaojuan Lu8Junxia Gu9Longwei Qiao10Qiping Zheng11Qiping Zheng12Department of Hematology and Hematological Laboratory Science, Jiangsu Key Laboratory of Medical Science and Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang, ChinaLaboratory of Clinical Medicine, Huai'an Women & Children Hospital, Affiliated to Yangzhou University, Huai'an, ChinaCenter of Clinical Laboratory, The First Affiliated Hospital of Soochow University, Suzhou, ChinaDepartment of Hematology and Hematological Laboratory Science, Jiangsu Key Laboratory of Medical Science and Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang, ChinaDepartment of Hematology and Hematological Laboratory Science, Jiangsu Key Laboratory of Medical Science and Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang, ChinaDepartment of Hematology and Hematological Laboratory Science, Jiangsu Key Laboratory of Medical Science and Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang, ChinaDepartment of Hematology and Hematological Laboratory Science, Jiangsu Key Laboratory of Medical Science and Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang, ChinaDepartment of Hematology and Hematological Laboratory Science, Jiangsu Key Laboratory of Medical Science and Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang, ChinaShenzhen Academy of Peptide Targeting Technology at Pingshan and Shenzhen Tyercan Bio-Pharm Co., Ltd., Shenzhen, ChinaDepartment of Hematology and Hematological Laboratory Science, Jiangsu Key Laboratory of Medical Science and Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang, ChinaSuzhou Affiliated to State Key Laboratory of Reproductive Medicine, School of Gusu, The Affiliated Suzhou Hospital of Nanjing Medical University, Nanjing Medical University, Suzhou, ChinaDepartment of Hematology and Hematological Laboratory Science, Jiangsu Key Laboratory of Medical Science and Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang, ChinaShenzhen Academy of Peptide Targeting Technology at Pingshan and Shenzhen Tyercan Bio-Pharm Co., Ltd., Shenzhen, ChinaHypertrophic chondrocytes and their specific marker, the type X collagen gene (Col10a1), are critical components of endochondral bone formation during skeletal development. We previously found that Runx2 is an indispensable mouse Col10a1 gene regulator and identified many other transcription factors (TFs) that potentially interact with the 150-bp Col10a1 cis-enhancer. However, the roles of these candidate TFs in Col10a1 expression and chondrocyte hypertrophy have not been elucidated. Here, we focus on 32 candidate TFs recently identified by analyzing the 150-bp Col10a1 enhancer using the transcription factor affinity prediction (TRAP) program. We found that 12 TFs (Hoxa3, Lsx, Evx2, Dlx5, S8, Pax2, Egr2, Mef2a, Barhl2, GKlf, Sox17, and Crx) were significantly upregulated and four TFs (Lhx4, Tbx5, Mef2c, and Hb9) were significantly downregulated in hypertrophic MCT cells, which show upregulation of Col10a1 expression. Most of the differential expression pattern of these TFs conformed with the results obtained from ATDC5 cell model and primary mouse chondrocytes. Notably, Tbx5 was downregulated upon Col10a1 upregulation, overexpression of Tbx5 decreased Col10a1 expression, and knock-down of Tbx5 increased Col10a1 expression in hypertrophic chondrocytes, suggesting that Tbx5 is a negative regulator of Col10a1. We further generated a stable Tbx5-overexpressing ATDC5 cell line and ColX-Tbx5 transgenic mice driven by Col10a1-specific enhancers and promoters. Tbx5 overexpression decreased Col10a1 expression in ATDC5 cells cultured as early as day 7 and in limb tissue on post-natal day 1. Slightly weaker alkaline phosphatase staining was also observed in cell culture on day 7 and in limb digits on embryonic day 17.5, indicating mildly delayed ossification. Further characterization of these candidate Col10a1 transcriptional regulators could help identify novel therapeutic targets for skeletal diseases associated with abnormal chondrocyte hypertrophy.https://www.frontiersin.org/articles/10.3389/fgene.2021.683939/fullCol10a1 regulatorsTbx-5Runx2TRAP programchondrocyte hypertrophyskeletal disease