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Transcriptome-wide map of m6A circRNAs identified in a rat model of hypoxia mediated pulmonary hypertension

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Abstract Background: Hypoxic pulmonary hypertension (HPH) is a lethal disease and lacks effective therapy. CircRNAs play significant roles in physiological process. Recently, circRNAs are found to be m6A-modified. The abundance of circRNAs was influenced by m6A. Furthermore, the significance of m6A circRNAs has not been elucidated in HPH yet. Here we aim to investigate the transcriptome-wide map of m6A circRNAs in HPH. Results: Differentially expressed m6A abundance was detected in lungs of HPH rats. M6A abundance in circRNAs was significantly reduced in hypoxia in vitro. M6A circRNAs were mainly from protein-coding genes spanned single exons in control and HPH groups. Moreover, m6A influenced the circRNA–miRNA–mRNA co-expression network in hypoxia. M6A circXpo6 and m6A circTmtc3 were firstly identified to be downregulated in HPH. Conclusion: Our study firstly identified the transcriptome-wide map of m6A circRNAs in HPH. M6A can influence circRNA–miRNA–mRNA network. Furthermore, we firstly identified two HPH-associated m6A circRNAs: circXpo6 and circTmtc3. However, the clinical significance of m6A circRNAs for HPH should be further validated. Key words: m6A circRNAs; hypoxic pulmonary hypertension; m6A circXpo6; m6A circTmtc3
Title: Transcriptome-wide map of m6A circRNAs identified in a rat model of hypoxia mediated pulmonary hypertension
Description:
Abstract Background: Hypoxic pulmonary hypertension (HPH) is a lethal disease and lacks effective therapy.
CircRNAs play significant roles in physiological process.
Recently, circRNAs are found to be m6A-modified.
The abundance of circRNAs was influenced by m6A.
Furthermore, the significance of m6A circRNAs has not been elucidated in HPH yet.
Here we aim to investigate the transcriptome-wide map of m6A circRNAs in HPH.
Results: Differentially expressed m6A abundance was detected in lungs of HPH rats.
M6A abundance in circRNAs was significantly reduced in hypoxia in vitro.
M6A circRNAs were mainly from protein-coding genes spanned single exons in control and HPH groups.
Moreover, m6A influenced the circRNA–miRNA–mRNA co-expression network in hypoxia.
M6A circXpo6 and m6A circTmtc3 were firstly identified to be downregulated in HPH.
Conclusion: Our study firstly identified the transcriptome-wide map of m6A circRNAs in HPH.
M6A can influence circRNA–miRNA–mRNA network.
Furthermore, we firstly identified two HPH-associated m6A circRNAs: circXpo6 and circTmtc3.
However, the clinical significance of m6A circRNAs for HPH should be further validated.
Key words: m6A circRNAs; hypoxic pulmonary hypertension; m6A circXpo6; m6A circTmtc3.

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Transcriptome-wide map of m6A circRNAs identified in a rat model of hypoxia mediated pulmonary hypertension
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