AUTHOR=Azumah Rafiatu , Hummitzsch Katja , Hartanti Monica D. , St. John Justin C. , Anderson Richard A. , Rodgers Raymond J. 

TITLE=Analysis of Upstream Regulators, Networks, and Pathways Associated With the Expression Patterns of Polycystic Ovary Syndrome Candidate Genes During Fetal Ovary Development

JOURNAL=Frontiers in Genetics

VOLUME=12

YEAR=2022

URL=https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2021.762177

DOI=10.3389/fgene.2021.762177

ISSN=1664-8021

ABSTRACT=<p>Polycystic Ovary Syndrome (PCOS) is a multifactorial syndrome with reproductive, endocrine, and metabolic symptoms, affecting about 10% women of reproductive age. Pathogenesis of the syndrome is poorly understood with genetic and fetal origins being the focus of the conundrum. Genetic predisposition of PCOS has been confirmed by candidate gene studies and Genome-Wide Association Studies (GWAS). Recently, the expression of PCOS candidate genes across gestation has been studied in human and bovine fetal ovaries. The current study sought to identify potential upstream regulators and mechanisms associated with PCOS candidate genes. Using RNA sequencing data of bovine fetal ovaries (62–276 days, <italic>n</italic> = 19), expression of PCOS candidate genes across gestation was analysed using Partek Flow. A supervised heatmap of the expression data of all 24,889 genes across gestation was generated. Most of the PCOS genes fell into one of four clusters according to their expression patterns. Some genes correlated negatively (early genes; <italic>C8H9orf3</italic>, <italic>TOX3</italic>, <italic>FBN3</italic>, <italic>GATA4</italic>, <italic>HMGA2</italic>, and <italic>DENND1A</italic>) and others positively (late genes; <italic>FDFT1</italic>, <italic>LHCGR</italic>, <italic>AMH</italic>, <italic>FSHR</italic>, <italic>ZBTB16</italic>, and <italic>PLGRKT</italic>) with gestational age. Pathways associated with PCOS candidate genes and genes co-expressed with them were determined using Ingenuity pathway analysis (IPA) software as well as DAVID Bioinformatics Resources for KEGG pathway analysis and Gene Ontology databases. Genes expressed in the early cluster were mainly involved in mitochondrial function and oxidative phosphorylation and their upstream regulators included <italic>PTEN</italic>, <italic>ESRRG/A</italic> and <italic>MYC</italic>. Genes in the late cluster were involved in stromal expansion, cholesterol biosynthesis and steroidogenesis and their upstream regulators included <italic>TGFB1/2/3</italic>, <italic>TNF, ERBB2/3</italic>, <italic>VEGF</italic>, <italic>INSIG1</italic>, <italic>POR</italic>, and <italic>IL25</italic>. These findings provide insight into ovarian development of relevance to the origins of PCOS, and suggest that multiple aetiological pathways might exist for the development of PCOS.</p>