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Whole genome analysis of alternative splicing in human placental decidual cells

https://doi.org/10.25557/2073-7998.2022.07.36-39

Abstract

Alternative splicing (AS) of mRNA is a key stage of post-transcriptional regulation of gene expression, which ensures the expression of various isoforms of RNA. Probably, this mechanism plays an important role in the development and functioning of the placenta. Decidual cells (DC) were chosen as the object of research due to their key role in physiological pregnancy. Whole transcriptome sequencing of DC RNA of placental tissue samples obtained from patients with the physiological pregnancy was performed, during which 151233 AS events in 352 genes were identified. It is noteworthy that two or more AS events characterized only 130 genes. These genes are involved in the canonical Wnt signaling pathway, regulation of substrate-dependent cell migration, activation of androgen receptors, and mRNA splicing. The maximum number of alternative events per gene established for the FN1 gene, the product of which is associated with the development of preeclampsia and is a screening marker of premature birth. The study suggests the prospects for further exploring of the distribution of alternatively spliced isoforms of the FN1 gene in a cohort of patients with both physiological pregnancy and obstetric pathology.

About the Authors

M. M. Gavrilenko
Research Institute of Medical Genetics, Tomsk National Research Medical Center of the Russian Academy of Sciences
Russian Federation


A. A. Babovskaya
Research Institute of Medical Genetics, Tomsk National Research Medical Center of the Russian Academy of Sciences
Russian Federation


A. A. Zarubin
Research Institute of Medical Genetics, Tomsk National Research Medical Center of the Russian Academy of Sciences
Russian Federation


E. A. Trifonova
Research Institute of Medical Genetics, Tomsk National Research Medical Center of the Russian Academy of Sciences
Russian Federation


V. A. Stepanov
Research Institute of Medical Genetics, Tomsk National Research Medical Center of the Russian Academy of Sciences
Russian Federation


References

1. Pan Q., Shai O., Lee L.J., et al. Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing. Nature genetics. 2008;40(12):1413-1415. DOI: 10.1038/ng.259

2. Raj T., Li Y.I., Wong G., et al.Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer’s disease susceptibility. Nature genetics. 2018;50(11):1584-1592. DOI: 10.1038/s41588-018-0238-1

3. Kahles A., Lehmann K., Toussaint N.C., et al.Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 Patients. Cancer Cell. 2018;34(2):211-224. DOI: 10.1016/j.ccell

4. Schatz F., Guzeloglu-Kayisli O., Arlier S., et al. The role of decidual cells in uterine hemostasis, menstruation, inflammation, adverse pregnancy outcomes and abnormal uterine bleeding. Human reproduction update. 2016;4:497-515. DOI: 10.1093/humupd/dmw004

5. Ladomery M.R., Harper S.J., Bates D.O. Alternative splicing in angiogenesis: the vascular endothelial growth factor paradigm. Cancer letters. 2007;249(2):133-142. DOI: 10.1016/j.canlet.2006.08.015

6. Robson S.C., Simpson H., Ball E., et al. Punch biopsy of the human placental bed. American journal of obstetrics and gynecology. 2002;187(5):1349-1355. DOI: 10.1067/mob.2002.126866

7. Goldstein L.D., Cao Y., Pau G., et al. Prediction and Quantification of Splice Events from RNA-Seq Data. PLoS One. 2016;11(5):e0156132. DOI: 10.1371/journal.pone.0156132

8. Bodova K.B., Biringer K., Dokus K., et al. Fibronectin, plasminogen activator inhibitor type 1 (PAI-1) and uterine artery Doppler velocimetry as markers of preeclampsia. Disease markers. 2011;30(4):191-196. DOI: 10.3233/DMA-2011-0772

9. Honest H, Bachmann LM, Gupta JK, et al. Accuracy of cervicovaginal fetal fibronectin test in predicting risk of spontaneous preterm birth: systematic review. BMJ. 2002;325(7359):301. DOI: 10.1136/bmj.325.7359.301

10. Paloschi V., Kurtovic S., Folkersen L., et al. Impaired splicing of fibronectin is associated with thoracic aortic aneurysm formation in patients with bicuspid aortic valve. Arteriosclerosis, thrombosis, and vascular biology. 2011;31(3):691-697. DOI: 10.1161/ATVBAHA.110.218461

11. Peters D.M., Mosher D.F. Localization of cell surface sites involved in fibronectin fibrillogenesis. The Journal of cell biology. 1987;104(1):121-130. DOI: 10.1161/ATVBAHA.110.21846

12. Krikun G., Lockwood C.J., Abrahams V.M., et al. Expression of toll-like receptors in the human decidua. Histology and histopathology. 2007;22(8):847-854. DOI: 10.14670/HH-22.847

13. Yeh C.C., Chao K.C., Huang S.J. Innate immunity, decidual cells, and preeclampsia. Reproductive Sciences. 2013;20(4):339-353. DOI: 10.1177/1933719112450330

14. Ruocco M.G., Chaouat G., Florez L., et al. Regulatory T-cells in pregnancy: historical perspective, state of the art, and burning questions. Frontiers in immunology. 2014;5:389. DOI: 10.3389/fimmu.2014.00389

15. Wu A., Liu F., Liu X., et al. Expression of TLR4 and its effect on Treg cells in early pregnancy decidual stromal cells after lipopolysaccharide treating. European Journal of Obstetrics & Gynecology and Reproductive Biology. 2019;237:209-214. DOI: 10.1016/j.ejogrb.2018.12.006


Review

For citations:


Gavrilenko M.M., Babovskaya A.A., Zarubin A.A., Trifonova E.A., Stepanov V.A. Whole genome analysis of alternative splicing in human placental decidual cells. Medical Genetics. 2022;21(7):36-39. (In Russ.) https://doi.org/10.25557/2073-7998.2022.07.36-39

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ISSN 2073-7998 (Print)