Ubiquitin-Proteasome-Collagen (CUP) Pathway in Preterm Premature Rupture of Fetal Membranes

• Published in: Frontiers in pharmacology Vol. 8; p. 310
• Main Authors: Zhao, Xinliang, Dong, Xiaoyan, Luo, Xiucui, Pan, Jing, Ju, Weina, Zhang, Meijiao, Wang, Peirong, Zhong, Mei, Yu, Yanhong, Brown, W. Ted, Zhong, Nanbert
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 02.06.2017
• Subjects: CNV; collagen; lncRNA; Pharmacology; SNV; sPTB; ubiquitin enzymes; CUP pathway; lncRNA; ubiquitin enzymes; collagen; UPS; CNV; SNV; sPTB
• ISSN: 1663-9812; 1663-9812
• DOI: 10.3389/fphar.2017.00310

Spontaneous preterm birth (sPTB) occurs before 37 gestational weeks, with preterm premature rupture of the membranes (PPROM) and spontaneous preterm labor (sPTL) as the predominant adverse outcomes. Previously, we identified altered expression of long non-coding RNAs (lncRNAs) and message RNAs (mRNAs) related to the ubiquitin proteasome system (UPS) in human placentas following pregnancy loss and PTB. We therefore hypothesized that similar mechanisms might underlie PPROM. In the current study, nine pairs of ubiquitin-proteasome-collagen (CUP) pathway-related mRNAs and associated lncRNAs were found to be differentially expressed in PPROM and sPTL. Pathway analysis showed that the functions of their protein products were inter-connected by ring finger protein. Twenty variants including five mutations were identified in CUP-related genes in sPTL samples. Copy number variations were found in COL19A1, COL28A1, COL5A1, and UBAP2 of sPTL samples. The results reinforced our previous findings and indicated the association of the CUP pathway with the development of sPTL and PPROM. This association was due not only to the genetic variation, but also to the epigenetic regulatory function of lncRNAs. Furthermore, the findings suggested that the loss of collagen content in PPROM could result from degradation and/or suppressed expression of collagens.