Genomic structure and expression of the human serotonin 2A receptor gene HTR2A locus: identification of novel HTR2A and antisense HTR2A-AS1 exonsReportar como inadecuado




Genomic structure and expression of the human serotonin 2A receptor gene HTR2A locus: identification of novel HTR2A and antisense HTR2A-AS1 exons - Descarga este documento en PDF. Documentación en PDF para descargar gratis. Disponible también para leer online.

BMC Genetics

, 17:16

First Online: 06 January 2016Received: 09 September 2015Accepted: 22 December 2015DOI: 10.1186-s12863-015-0325-6

Cite this article as: Ruble, C.L., Smith, R.M., Calley, J. et al. BMC Genet 2016 17: 16. doi:10.1186-s12863-015-0325-6

Abstract

BackgroundThe serotonin 2A receptor is widely implicated in genetic association studies and remains an important drug target for psychiatric, neurological, and cardiovascular conditions. RNA sequencing redefined the architecture of the serotonin 2A receptor gene HTR2A, revealing novel mRNA transcript isoforms utilizing unannotated untranslated regions of the gene. Expression of these untranslated regions is modulated by common single nucleotide polymorphisms SNPs, namely rs6311. Previous studies did not fully capture the complexity of the sense- and antisense-encoded transcripts with respect to novel exons in the HTR2A gene locus. Here, we comprehensively catalogued exons and RNA isoforms for both HTR2A and HTR2A-AS1 using RNA-Seq from human prefrontal cortex and multiple mouse tissues. We subsequently tested associations between expression of newfound gene features and common SNPs in humans.

ResultsWe find that the human HTR2A gene spans ~66 kilobases and consists of 7, rather than 4 exons. Furthermore, the revised human HTR2A-AS1 gene spans ~474 kilobases and consists of 18, rather than 3 exons. Three HTR2A exons directly overlap with HTR2A-AS1 exons, suggesting potential for complementary nucleotide interactions. The repertoire of possible mouse Htr2a splice isoforms is remarkably similar to humans and we also find evidence for overlapping sense-antisense transcripts in the same relative positions as the human transcripts. rs6311 and SNPs in high linkage disequilibrium are associated with HTR2A-AS1 expression, in addition to previously described associations with expression of the extended 5’ untranslated region of HTR2A.

ConclusionsOur proposed HTR2A and HTR2A-AS1 gene structures dramatically differ from current annotations, now including overlapping exons on the sense and anti-sense strands. We also find orthologous transcript isoforms expressed in mice, providing opportunities to elucidate the biological roles of the human isoforms using a model system. Associations between rs6311 and expression of HTR2A and HTR2A-AS1 suggest this polymorphism is capable of modulating the expression of the sense or antisense transcripts. Still unclear is whether these SNPs act directly on the expression of the sense or antisense transcripts and whether overlapping exons are capable of interacting through complimentary base-pairing. Additional studies are necessary to determine the extent and nature of interactions between the SNPs and the transcripts prior to interpreting these findings in the context of phenotypes associated with HTR2A.

KeywordsSerotonin HTR2A Alternative splicing Antisense RNA mRNA expression Regulatory polymorphism Allelic expression Comparative genomics Long non-coding RNA 5-HT2A Electronic supplementary materialThe online version of this article doi:10.1186-s12863-015-0325-6 contains supplementary material, which is available to authorized users.

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Autor: Cara L. Ruble - Ryan M. Smith - John Calley - Leanne Munsie - David C. Airey - Yuan Gao - Joo Heon Shin - Thomas M. H

Fuente: https://link.springer.com/







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