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Published in: Pediatric Surgery International 9/2018

01-09-2018 | Original Article

Integrating lncRNAs and mRNAs expression profiles in terminal hindgut of fetal rats with anorectal malformations

Authors: Hui Xiao, Rui Huang, Long Chen, Mei Diao, Long Li

Published in: Pediatric Surgery International | Issue 9/2018

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Abstract

Background

The detailed embryonic etiology and pathogenesis of anorectal malformations (ARMs) remains unclear. Recent studies have shown that gene expression abnormalities were the key factors that result in ARMs. Long non-coding RNAs (lncRNAs) were reported as the ‘transcriptional noise’ within the genome. The expression profiles of lncRNA and mRNA remain less characterized in the pathogenesis of ARMs. Furthermore, the function of lncRNAs in the regulation of this process has not been investigated so far. Therefore, this current study was aimed to integrate lncRNA and mRNA expression profiles in terminal hindgut of ethylenethiourea (ETU)-induced ARM rats using Agilents lncRNA and mRNA co-expression microarrays.

Methods

ARM model was induced with ethylenethiourea (ETU) on gestational day 10. Cesarean deliveries were conducted to collect the embryos on gestational day 20. For the extraction of total RNA, 1-cm terminal hindgut tissues were collected from three fetal rats with similair weights. The microarrays and quantitative RT-PCR analysis were conducted to evaluate the lncRNA and mRNA expression profiles in normal fetal rats and ARM fetal rats.

Results

Compared with control group, 164 lncRNAs were observed to be aberrantly expressed (FC ≥ 2; P < 0.05) in ARM group, including 36 upregulated and 128 downregulated, while 772 mRNAs were observed to be aberrantly expressed (FC ≥ 2; P < 0.05) in the terminal hindgut, including 350 up-regulated and 422 down-regulated. The differential expression profiles between the ARM and the control group were used for gene ontology (GO) and pathway analysis. A subset of those RNAs was identified to be closely related to the development process of ARMs. The four RNAs that were differentially expressed between the two groups were selected for qPCR validation, and the results were in line with the microarray data. In addition, the lncRNAs and mRNA co-expression network was established according to the correlation analysis. We predicted the functions of transregulatory lncRNAs by the TFs (transcription factors) which might modulate their expression. In the core network of lncRNA–TF pairs, the lncRNAs can be classified into 5 categories of pathways governed by Jun, c-Myc, Usf1, Alf2, and Stat3.

Conclusion

From the above results, it can be suggested that these aberrant lncRNAs might participate in the pathogenesis of ARM, and our present work may provide new research directions for future studies of ARMs.
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Literature
2.
go back to reference Bai Y, Yuan Z, Wang W et al (2000) Quality of life for children with fecal incontinence after surgically corrected anorectal malformation. J Pediatr Surg 35(3):462–464CrossRefPubMed Bai Y, Yuan Z, Wang W et al (2000) Quality of life for children with fecal incontinence after surgically corrected anorectal malformation. J Pediatr Surg 35(3):462–464CrossRefPubMed
3.
go back to reference Levitt MA, Peña A (2005) Outcomes from the correction of anorectal malformations. Curr Opin Pediatr 17(3):394–401CrossRefPubMed Levitt MA, Peña A (2005) Outcomes from the correction of anorectal malformations. Curr Opin Pediatr 17(3):394–401CrossRefPubMed
4.
go back to reference Peña A, Guardino K, Levitt MA et al (1998) Bowel management for fecal incontinence in patients with anorectal malformations. J Pediatr Surg 33(1):133–137CrossRefPubMed Peña A, Guardino K, Levitt MA et al (1998) Bowel management for fecal incontinence in patients with anorectal malformations. J Pediatr Surg 33(1):133–137CrossRefPubMed
5.
go back to reference Endo M, Hayashi A, Ishihara M et al (1999) Analysis of 1992 patients with anorectal malformations over the past two decades in Japan. Steering Committee of Japanese Study Group of Anorectal Anomalies. J Pediatr Surg 34(3):435–441CrossRefPubMed Endo M, Hayashi A, Ishihara M et al (1999) Analysis of 1992 patients with anorectal malformations over the past two decades in Japan. Steering Committee of Japanese Study Group of Anorectal Anomalies. J Pediatr Surg 34(3):435–441CrossRefPubMed
6.
go back to reference Wang C, Li L, Cheng W (2015) Anorectal malformation: the etiological factors. Pediatr Surg Int 31(9):795–804CrossRefPubMed Wang C, Li L, Cheng W (2015) Anorectal malformation: the etiological factors. Pediatr Surg Int 31(9):795–804CrossRefPubMed
8.
go back to reference Liu H, Chen P, Jiang C et al (2016) Screening for the key lncRNA targets associated with metastasis of renal clear cell carcinoma. Medicine (Baltimore) 95(2):e2507CrossRef Liu H, Chen P, Jiang C et al (2016) Screening for the key lncRNA targets associated with metastasis of renal clear cell carcinoma. Medicine (Baltimore) 95(2):e2507CrossRef
9.
go back to reference Lan X, Yan J, Ren J et al (2016) A novel long noncoding RNA Lnc-HC binds hnRNPA2B1 to regulate expressions of Cyp7a1 and Abca1 in hepatocytic cholesterol metabolism. Hepatology 64(1):58–72CrossRefPubMed Lan X, Yan J, Ren J et al (2016) A novel long noncoding RNA Lnc-HC binds hnRNPA2B1 to regulate expressions of Cyp7a1 and Abca1 in hepatocytic cholesterol metabolism. Hepatology 64(1):58–72CrossRefPubMed
10.
go back to reference Wang K, Liu CY, Zhou LY et al (2015) APF lncRNA regulates autophagy and myocardial infarction by targeting miR-188-3p. Nat Commun 6:6779CrossRefPubMed Wang K, Liu CY, Zhou LY et al (2015) APF lncRNA regulates autophagy and myocardial infarction by targeting miR-188-3p. Nat Commun 6:6779CrossRefPubMed
12.
go back to reference Vausort M, Wagner DR, Devaux Y (2014) Long noncoding RNAs in patients with acute myocardial infarction. Circ Res 115(7):668–677CrossRefPubMed Vausort M, Wagner DR, Devaux Y (2014) Long noncoding RNAs in patients with acute myocardial infarction. Circ Res 115(7):668–677CrossRefPubMed
13.
14.
go back to reference Han L, Zhang K, Shi Z et al (2012) LncRNA profile of glioblastoma reveals the potential role of lncRNAs in contributing to glioblastoma pathogenesis. Int J Oncol 40(6):2004–2012PubMed Han L, Zhang K, Shi Z et al (2012) LncRNA profile of glioblastoma reveals the potential role of lncRNAs in contributing to glioblastoma pathogenesis. Int J Oncol 40(6):2004–2012PubMed
15.
go back to reference Marini KD, Payne BJ, Watkins DN et al (2011) Mechanisms of Hedgehog signaling in cancer. Growth Factors 29(6):221–234CrossRefPubMed Marini KD, Payne BJ, Watkins DN et al (2011) Mechanisms of Hedgehog signaling in cancer. Growth Factors 29(6):221–234CrossRefPubMed
17.
go back to reference Carter TC, Kay DM, Browne ML et al (2013) Anorectal atresia and variants at predicted regulatory sites in candidate genes. Ann Hum Genet 77(1):31–46CrossRefPubMed Carter TC, Kay DM, Browne ML et al (2013) Anorectal atresia and variants at predicted regulatory sites in candidate genes. Ann Hum Genet 77(1):31–46CrossRefPubMed
18.
go back to reference Garcia-Barceló MM, Chi-Hang Lui V, Miao X et al (2008) Mutational analysis of SHH and GLI3 in anorectal malformations. Birth Defects Res A Clin Mol Teratol 82(9):644–648CrossRefPubMed Garcia-Barceló MM, Chi-Hang Lui V, Miao X et al (2008) Mutational analysis of SHH and GLI3 in anorectal malformations. Birth Defects Res A Clin Mol Teratol 82(9):644–648CrossRefPubMed
19.
go back to reference Zhang J, Zhang ZB, Gao H et al (2009) Down-regulation of SHH/BMP4 signalling in human anorectal malformations. J Int Med Res 37(6):1842–1850CrossRefPubMed Zhang J, Zhang ZB, Gao H et al (2009) Down-regulation of SHH/BMP4 signalling in human anorectal malformations. J Int Med Res 37(6):1842–1850CrossRefPubMed
20.
go back to reference Huang Y, Zhang P, Zheng S et al (2014) Hypermethylation of SHH in the pathogenesis of congenital anorectal malformations. J Pediatr Surg 49(9):1400–1404CrossRefPubMed Huang Y, Zhang P, Zheng S et al (2014) Hypermethylation of SHH in the pathogenesis of congenital anorectal malformations. J Pediatr Surg 49(9):1400–1404CrossRefPubMed
21.
go back to reference Jia H, Chen Q, Zhang T et al (2011) Wnt5a expression in the hindgut of fetal rats with chemically induced anorectal malformations—studies in the ETU rat model. Int J Colorectal Dis 26(4):493–499CrossRefPubMed Jia H, Chen Q, Zhang T et al (2011) Wnt5a expression in the hindgut of fetal rats with chemically induced anorectal malformations—studies in the ETU rat model. Int J Colorectal Dis 26(4):493–499CrossRefPubMed
22.
23.
go back to reference Geng Y, Mi J, Gao H et al (2017) Spatiotemporal expression of Wnt3a during striated muscle complex development in rat embryos with ethylenethiourea-induced anorectal malformations. Mol Med Rep 15(4):1601–1606CrossRefPubMedPubMedCentral Geng Y, Mi J, Gao H et al (2017) Spatiotemporal expression of Wnt3a during striated muscle complex development in rat embryos with ethylenethiourea-induced anorectal malformations. Mol Med Rep 15(4):1601–1606CrossRefPubMedPubMedCentral
24.
go back to reference Ng RC, Matsumaru D, Ho AS et al (2014) Dysregulation of Wnt inhibitory factor 1 (Wif1) expression resulted in aberrant Wnt-beta-catenin signaling and cell death of the cloaca endoderm, and anorectal malformations. Cell Death Differ 21(6):978–989CrossRefPubMedPubMedCentral Ng RC, Matsumaru D, Ho AS et al (2014) Dysregulation of Wnt inhibitory factor 1 (Wif1) expression resulted in aberrant Wnt-beta-catenin signaling and cell death of the cloaca endoderm, and anorectal malformations. Cell Death Differ 21(6):978–989CrossRefPubMedPubMedCentral
26.
go back to reference Brafman D, Willert K (2017) Wnt/beta-catenin signaling during early vertebrate neural development. Dev Neurobiol 77(11):1239–1259CrossRefPubMed Brafman D, Willert K (2017) Wnt/beta-catenin signaling during early vertebrate neural development. Dev Neurobiol 77(11):1239–1259CrossRefPubMed
27.
go back to reference Khanna K, Sharma S, Pabalan N et al (2018) A review of genetic factors contributing to the etiopathogenesis of anorectal malformations. Pediatr Surg Int 34(1):9–20CrossRefPubMed Khanna K, Sharma S, Pabalan N et al (2018) A review of genetic factors contributing to the etiopathogenesis of anorectal malformations. Pediatr Surg Int 34(1):9–20CrossRefPubMed
28.
go back to reference Camon E, Magrane M, Barrell D et al (2004) The gene ontology annotation (GOA) database: sharing knowledge in Uniprot with Gene Ontology. Nucleic Acids Res 32(Database issue):D262–D266CrossRefPubMedPubMedCentral Camon E, Magrane M, Barrell D et al (2004) The gene ontology annotation (GOA) database: sharing knowledge in Uniprot with Gene Ontology. Nucleic Acids Res 32(Database issue):D262–D266CrossRefPubMedPubMedCentral
29.
go back to reference Du J, Li M, Yuan Z et al (2016) A decision analysis model for KEGG pathway analysis. BMC Bioinform 17(1):407CrossRef Du J, Li M, Yuan Z et al (2016) A decision analysis model for KEGG pathway analysis. BMC Bioinform 17(1):407CrossRef
30.
go back to reference Ma H, Hao Y, Dong X et al (2012) Molecular mechanisms and function prediction of long noncoding RNA. Sci World J 2012:541786 Ma H, Hao Y, Dong X et al (2012) Molecular mechanisms and function prediction of long noncoding RNA. Sci World J 2012:541786
31.
go back to reference Kim ED, Sung S (2012) Long noncoding RNA: unveiling hidden layer of gene regulatory networks. Trends Plant Sci 17(1):16–21CrossRefPubMed Kim ED, Sung S (2012) Long noncoding RNA: unveiling hidden layer of gene regulatory networks. Trends Plant Sci 17(1):16–21CrossRefPubMed
32.
go back to reference De Lucia F, Dean C (2011) Long non-coding RNAs and chromatin regulation. Curr Opin Plant Biol 14(2):168–173CrossRefPubMed De Lucia F, Dean C (2011) Long non-coding RNAs and chromatin regulation. Curr Opin Plant Biol 14(2):168–173CrossRefPubMed
Metadata
Title
Integrating lncRNAs and mRNAs expression profiles in terminal hindgut of fetal rats with anorectal malformations
Authors
Hui Xiao
Rui Huang
Long Chen
Mei Diao
Long Li
Publication date
01-09-2018
Publisher
Springer Berlin Heidelberg
Published in
Pediatric Surgery International / Issue 9/2018
Print ISSN: 0179-0358
Electronic ISSN: 1437-9813
DOI
https://doi.org/10.1007/s00383-018-4311-8

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