Genetic Variation at Chromosome 2q13 and Its Potential Influence on Endometriosis Susceptibility Through Effects on the IL-1 Family

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This study analyzed the 2q13 chromosomal region, identifying 21 transcripts including six IL-1 family genes, suggesting their altered expression may influence endometriosis susceptibility via inflammation.

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The paper analyzed the chromosome 2q13 genomic region around endometriosis GWAS sentinel SNP rs10167914, focusing on an inflammation-rich transcript area and specifically on 6 interleukin (IL)-1 family genes among 21 transcripts within ~250 kb. It reported identifying multiple gene types (interleukin family, previously reported inflammation-related coding genes, novel coding/pseudogenes, and noncoding RNAs) and then used an extensive literature review to assess roles of these genes and proteins in endometriosis pathogenesis. The authors concluded that altered IL-1 family transcript expression, either alone or as a combined inflammatory milieu, could influence endometriosis and should be prioritized for future investigation, while noting that their functional implications are inferred from genomic mapping and literature rather than directly tested experimentally. This paper is centrally about endometriosis — it links a 2q13 endometriosis risk locus to IL-1 family inflammatory gene regulation as a possible contributor to disease mechanisms.

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Abstract

Endometriosis is characterized by the growth of epithelial and stromal cells outside the uterine cavity. It has a complex etiology and affects ∼10% of reproductive age women. It is accompanied by a chronic inflammatory response with substantial evidence to indicate genetic susceptibility. The causal genes and their pathways leading to endometriosis, however, are still unknown. Recently, genomewide association studies on endometriosis identified 14 genomic risk loci in women of European and Japanese ancestry. It is becoming increasingly clear that these risk regions are intergenic and thus contribute to disease susceptibility through regulatory mechanisms, most likely mediated through regulation of genes within a restricted distance from the risk variants. One endometriosis risk locus has been detected at chromosome 2q13 within an inflammatory-rich region of gene transcripts and thus may play a role in the inflammation component of the disease. We carried out detailed analysis of the genomic region 250 kb on either side of sentinel SNP rs10167914 and identified 21 transcripts which contained 6 interleukin (IL)-1 family genes, 3 previously reported coding genes that have a relationship to inflammation, 4 novel coding, or pseudogenes, and 8 noncoding RNA transcripts. Through an extensive literature search, we examined the roles these genes and their resultant proteins play in endometriosis pathogenesis. The results suggest alteration in the expression the IL-1 family transcripts either alone or as a complex milieu could have a significant influence on endometriosis and should be prioritized for future study on the implications of inflammation on endometriotic lesions.
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Abstract

Endometriosis is characterized by the growth of epithelial and stromal cells outside the uterine cavity. It has a complex etiology and affects ≈10% of reproductive age women. It is accompanied by a chronic inflammatory response with substantial evidence to indicate genetic susceptibility. The causal genes and their pathways leading to endometriosis, however, are still unknown. Recently, genomewide association studies on endometriosis identified 14 genomic risk loci in women of European and Japanese ancestry. It is becoming increasingly clear that these risk regions are intergenic and thus contribute to disease susceptibility through regulatory mechanisms, most likely mediated through regulation of genes within a restricted distance from the risk variants. One endometriosis risk locus has been detected at chromosome 2q13 within an inflammatory-rich region of gene transcripts and thus may play a role in the inflammation component of the disease. We carried out detailed analysis of the genomic region 250 kb on either side of sentinel SNP rs10167914 and identified 21 transcripts which contained 6 interleukin (IL)-1 family genes, 3 previously reported coding genes that have a relationship to inflammation, 4 novel coding, or pseudogenes, and 8 noncoding RNA transcripts. Through an extensive literature search, we examined the roles these genes and their resultant proteins play in endometriosis pathogenesis. The results suggest alteration in the expression the IL-1 family transcripts either alone or as a complex milieu could have a significant influence on endometriosis and should be prioritized for future study on the implications of inflammation on endometriotic lesions. Similar content being viewed by others

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Sci. 25, 1307–1317 (2018). https://doi.org/10.1177/1933719118768688 Published: Version of record: Issue date: DOI: https://doi.org/10.1177/1933719118768688

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endometriosis

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Chromosomes, Human, Pair 2 Endometriosis Genetic Predisposition to Disease Genetic Variation Interleukin-1 Endometriosis Female Humans Interleukin-1 Polymorphism, Single Nucleotide

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