Comprehensive analysis of differentially expressed profiles of non-coding RNAs in peripheral blood and ceRNA regulatory networks in non-syndromic orofacial clefts

被引:17
作者
Gao, Yuwei [1 ]
Zang, Qiguang [1 ]
Song, Hongquan [1 ]
Fu, Songbin [2 ]
Sun, Wenjing [2 ]
Zhang, Wei [3 ]
Wang, Xiaotong [1 ]
Li, Yong [1 ]
Jiao, Xiaohui [1 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 1, Dept Oral Maxillofacial Surg, 23 Youzheng St, Harbin 150001, Heilongjiang, Peoples R China
[2] Harbin Med Univ, Lab Med Genet, Harbin 150081, Heilongjiang, Peoples R China
[3] Harbin Med Univ, Affiliated Hosp 4, Dept Oral Maxillofacial Surg, Harbin 150001, Heilongjiang, Peoples R China
关键词
long non-coding RNA; microRNA; mRNA; RNA sequencing; ceRNA; non-syndromic orofacial clefts; GENE-EXPRESSION; MICRORNA EXPRESSION; TGF-BETA; MATRIX METALLOPROTEINASES; PALATE; LIP; TRANSCRIPTOME; FIBROBLASTS; INHIBITORS; APOPTOSIS;
D O I
10.3892/mmr.2019.10261
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Non-syndromic orofacial clefts (NSOC), which include cleft lip with or without cleft palate (CL/P) and cleft palate only (CPO), are common congenital birth defects in humans. Accumulating evidence indicates that long non-coding RNAs (lncRNAs) and microRNAs (miRNAs or miRs) play important roles in NSOC; however, the potential regulatory associations between them remain largely unknown. In this study, we performed next-generation RNA sequencing (RNA-seq) to identify transcriptome profiles, including mRNAs, lncRNAs and miRNAs, in patients with CL/P and CPO. A total of 36 lncRNAs, 1,341 mRNAs and 60 miRNAs were found to be differentially expressed in the CL/P group compared to the control group, and 57 lncRNAs, 1,255 mRNAs and 162 miRNAs were found to be differentially expressed in the CPO group compared to the control group. Subsequently, reverse transcription-quantitative polymerase chain reaction (RT-qPCR) was performed to validate the expression of selected lncRNAs, miRNAs and mRNAs. In addition, bioinformatics methods were employed to explore the potential functions of ncRNAs and to construct lncRNA-miRNA-mRNA regulatory networks. To the best of our knowledge, this is the first study to comprehensively analyze regulated non-coding RNAs (ncRNAs) in CL/P and CPO, providing a novel perspective on the etiology of NSOC and laying the foundation for future research into the potential regulatory mechanisms of ncRNAs and mRNAs in NSOC.
引用
收藏
页码:513 / 528
页数:16
相关论文
共 75 条
[1]   Human Cleft Lip and Palate Fibroblasts and Normal Nicotine-Treated Fibroblasts Show Altered In Vitro Expressions of Genes Related to Molecular Signaling Pathways and Extracellular Matrix Metabolism [J].
Baroni, Tiziano ;
Bellucci, Catia ;
Lilli, Cinzia ;
Pezzetti, Furio ;
Carinci, Francesco ;
Lumare, Eleonora ;
Palmieri, Annalisa ;
Stabellini, Giordano ;
Bodo, Maria .
JOURNAL OF CELLULAR PHYSIOLOGY, 2010, 222 (03) :748-756
[2]   A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4 [J].
Beaty, Terri H. ;
Murray, Jeffrey C. ;
Marazita, Mary L. ;
Munger, Ronald G. ;
Ruczinski, Ingo ;
Hetmanski, Jacqueline B. ;
Liang, Kung Yee ;
Wu, Tao ;
Murray, Tanda ;
Fallin, M. Daniele ;
Redett, Richard A. ;
Raymond, Gerald ;
Schwender, Holger ;
Jin, Sheng-Chih ;
Cooper, Margaret E. ;
Dunnwald, Martine ;
Mansilla, Maria A. ;
Leslie, Elizabeth ;
Bullard, Stephen ;
Lidral, Andrew C. ;
Moreno, Lina M. ;
Menezes, Renato ;
Vieira, Alexandre R. ;
Petrin, Aline ;
Wilcox, Allen J. ;
Lie, Rolv T. ;
Jabs, Ethylin W. ;
Wu-Chou, Yah Huei ;
Chen, Philip K. ;
Wang, Hong ;
Ye, Xiaoqian ;
Huang, Shangzhi ;
Yeow, Vincent ;
Chong, Samuel S. ;
Jee, Sun Ha ;
Shi, Bing ;
Christensen, Kaare ;
Melbye, Mads ;
Doheny, Kimberly F. ;
Pugh, Elizabeth W. ;
Ling, Hua ;
Castilla, Eduardo E. ;
Czeizel, Andrew E. ;
Ma, Lian ;
Field, L. Leigh ;
Brody, Lawrence ;
Pangilinan, Faith ;
Mills, James L. ;
Molloy, Anne M. ;
Kirke, Peadar N. .
NATURE GENETICS, 2010, 42 (06) :525-U76
[3]   Runx1 is involved in the fusion of the primary and the secondary palatal shelves [J].
Charoenchaikorn, Kesinee ;
Yokomizo, Tomomasa ;
Rice, David P. ;
Honjo, Tadashi ;
Matsuzaki, Kiyomi ;
Shintaku, Yuko ;
Imai, Yuichi ;
Wakamatsu, Asami ;
Takahashi, Satoru ;
Ito, Yoshiaki ;
Takano-Yamamoto, Teruko ;
Thesleff, Irma ;
Yamamoto, Masayuki ;
Yamashiro, Takashi .
DEVELOPMENTAL BIOLOGY, 2009, 326 (02) :392-402
[4]  
CHENEVIXTRENCH G, 1992, AM J HUM GENET, V51, P1377
[5]   Knockdown of Crispld2 in zebrafish identifies a novel network for nonsyndromic cleft lip with or without cleft palate candidate genes [J].
Chiquet, Brett T. ;
Yuan, Qiuping ;
Swindell, Eric C. ;
Maili, Lorena ;
Plant, Robert ;
Dyke, Jeffrey ;
Boyer, Ryan ;
Teichgraeber, John F. ;
Greives, Matthew R. ;
Mulliken, John B. ;
Letra, Ariadne ;
Blanton, Susan H. ;
Hecht, Jacqueline T. .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 (10) :1441-1450
[6]   Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate [J].
Chiquet, Brett T. ;
Hashmi, Syed S. ;
Henry, Robin ;
Burt, Amber ;
Mulliken, John B. ;
Stal, Samuel ;
Bray, Molly ;
Blanton, Susan H. ;
Hecht, Jacqueline T. .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2009, 17 (02) :195-204
[7]   Role of Apoptosis in Retinoic Acid-Induced Cleft Palate [J].
Choi, Jong Woo ;
Park, Hyung Woo ;
Kwon, Yoon Jeong ;
Park, Beyoung Yoon .
JOURNAL OF CRANIOFACIAL SURGERY, 2011, 22 (05) :1567-1571
[8]   Long term follow up study of survival associated with cleft lip and palate at birth [J].
Christensen, K ;
Juel, K ;
Herskind, M ;
Murray, JC .
BRITISH MEDICAL JOURNAL, 2004, 328 (7453) :1405-1406
[9]   Overexpression of Smad2 in Tgf-β3-null mutant mice rescues cleft palate [J].
Cui, XM ;
Shiomi, N ;
Chen, JC ;
Saito, T ;
Yamamoto, T ;
Ito, Y ;
Bringas, P ;
Chat, Y ;
Shuler, CF .
DEVELOPMENTAL BIOLOGY, 2005, 278 (01) :193-202
[10]   Irf6-Related Gene Regulatory Network Involved in Palate and Lip Development [J].
Dai, Jiewen ;
Yu, Hongbo ;
Si, Jiawen ;
Fang, Bing ;
Shen, Steve Guofang .
JOURNAL OF CRANIOFACIAL SURGERY, 2015, 26 (05) :1600-1605