Zhao Xinliang, Dong Xiaoyan, Luo Xiucui, Pan Jing, Ju Weina, Zhang Meijiao, Wang Peirong, Zhong Mei, Yu Yanhong, Brown W Ted, Zhong Nanbert
Lianyungang Maternal and Children's HospitalLianyungang, China.
Peking University Center of Medical Genetics, Peking University Health Science CenterBeijing, China.
Front Pharmacol. 2017 Jun 2;8:310. doi: 10.3389/fphar.2017.00310. eCollection 2017.
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.
自发性早产(sPTB)发生在妊娠37周之前,胎膜早破(PPROM)和自发性早产(sPTL)是主要不良结局。此前,我们发现流产和早产后人胎盘组织中与泛素蛋白酶体系统(UPS)相关的长链非编码RNA(lncRNAs)和信使RNA(mRNAs)表达发生改变。因此,我们推测PPROM可能存在类似机制。在本研究中,发现9对泛素-蛋白酶体-胶原蛋白(CUP)途径相关的mRNAs和相关lncRNAs在PPROM和sPTL中差异表达。通路分析表明,其蛋白质产物的功能通过泛素连接酶相互关联。在sPTL样本的CUP相关基因中鉴定出20个变异,包括5个突变。在sPTL样本的COL19A1、COL28A1、COL5A1和UBAP2中发现了拷贝数变异。这些结果强化了我们之前的发现,并表明CUP途径与sPTL和PPROM的发生有关。这种关联不仅归因于基因变异,还归因于lncRNAs的表观遗传调控功能。此外,研究结果表明,PPROM中胶原蛋白含量的减少可能是由于胶原蛋白的降解和/或表达受抑制所致。