bioRxiv Science⌕ Search

bioRxiv · 10.1101/668376

Aligning RNA-Seq reads to a sex chromosome complement informed reference genome increases ability to detect sex differences in gene expression

Abstract

BackgroundHuman X and Y chromosomes share an evolutionary origin and, as a consequence, sequence similarity. We investigated whether sequence homology between the X and Y chromosomes affects alignment of RNA-Seq reads and estimates of differential expression. We tested the effects of using reference genomes and reference transcriptomes informed by the sex chromosome complement of the samples genome on measurements of RNA-Seq abundance and sex differences in expression. ResultsThe default genome includes the entire human reference genome (GRCh38), including the entire sequence of the X and Y chromosomes. We created two sex chromosome complement informed reference genomes. One sex chromosome complement informed reference genome was used for samples that lacked a Y chromosome; for this reference genome version, we hard-masked the entire Y chromosome. For the other sex chromosome complement informed reference genome, to be used for samples with a Y chromosome, we hard-masked only the pseudoautosomal regions of the Y chromosome, because these regions are duplicated identically in the reference genome on the X chromosome. We analyzed transcript abundance in the whole blood, brain cortex, breast, liver, and thyroid tissues from 20 genetic female (46, XX) and 20 genetic male (46, XY) samples. Each sample was aligned twice; once to the default reference genome and then independently aligned to a reference genome informed by the sex chromosome complement of the sample, repeated using two different read aligners, HISAT and STAR. We then quantified sex differences in gene expression using featureCounts to get the raw count estimates followed by Limma/Voom for normalization and differential expression. We additionally created sex chromosome complement informed transcriptome references for use in pseudo-alignment using Salmon. Transcript abundance was quantified twice for each sample; once to the default target transcripts and then independently to target transcripts informed by the sex chromosome complement of the sample. ConclusionsWe show that regardless of the choice of read aligner, using an alignment protocol informed by the sex chromosome complement of the sample results in higher expression estimates on the pseudoautosomal regions of the X chromosome in both genetic male and genetic female samples, as well as an increased number of unique genes being called as differentially expressed between the sexes. We additionally show that using a pseudo-alignment approach informed on the sex chromosome complement of the sample eliminates Y-linked expression in female XX samples. Author summaryThe human X and Y chromosomes share an evolutionary origin and sequence homology, including regions of 100% identity; this sequence homology can result in reads misaligning between the sex chromosomes, X and Y. We hypothesized that misalignment of reads on the sex chromosomes would confound estimates of transcript abundance if the sex chromosome complement of the sample is not accounted for during the alignment step. For example, because of shared sequence similarity, X-linked reads could misalign to the Y chromosome. This is expected to result in reduced expression for regions between X and Y that share high levels of homology. For this reason, we tested the effect of using a default reference genome versus a reference genome informed by the sex chromosome complement of the sample on estimates of transcript abundance in human RNA-Seq samples from whole blood, brain cortex, breast, liver, and thyroid tissues of 20 genetic female (46, XX) and 20 genetic male (46, XY) samples. We found that using a reference genome with the sex chromosome complement of the sample resulted in higher measurements of X-linked gene transcription for both male and female samples and more differentially expressed genes on the X and Y chromosomes. We additionally investigated the use of a sex chromosome complement informed transcriptome reference index for alignment free quantification protocols. We observed no Y-linked expression in female XX samples only when the transcript quantification was performed using a transcriptome reference index informed on the sex chromosome complement of the sample. We recommend that future studies requiring aligning RNA-Seq reads to a reference genome or pseudo-alignment with a transcriptome reference should consider the sex chromosome complement of their samples prior to running default pipelines.

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Olney, K. C., Brotman, S. M., Valverde-Vesling, V., Andrews, J., Wilson, M. A.. 2019-06-12. Aligning RNA-Seq reads to a sex chromosome complement informed reference genome increases ability to detect sex differences in gene expression. https://doi.org/10.1101/668376

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

A timeline for evolution of metabolism in early microbes

The metabolism of early microbes shaped our planet's chemistry and enabled more life to evolve. However, it remains uncertain when many forms of metabolism arose and which organisms carried them out. Here we combine machine learning, metabolic networks, and phylogenomics of microbes to date 14 forms of metabolism and 6 other traits. We find that metabolism evolved in three waves, starting >3.4 billion years ago (Ga) with fermentation and sulfur compound respiration. A second wave began ~3.2 Ga with aerobic respiration and growth, while a third began ~1.4 Ga with further specialization. We compared these predictions with independent dates from the geochemical record, and agreement with conservative dates was good (CCC = 0.81 to 0.89). Several forms of metabolism are invisible in the geochemical record, and our approach dates these forms, too. Our results reconcile different lines of evidence for microbial evolution and provide a fuller picture of early Earth.

evolutionary biology↗

Sexual interactions and local selection shape reproductive gene diversity and divergence

Genes involved in genotype x genotype coevolution display unique patterns of nucleotide diversity and population divergence. In Drosophila melanogaster, Sex Peptide is a key sperm competition gene that is an outlier for both pi within populations and Fst between populations. This pattern is not predicted by current theoretical expectations of selective sweeps highlighting the need to develop predictions to identify genes experiencing balancing selection. We compared pi and FST in D. melanogaster populations to identify other genes following a co-evolutionary model that generates divergence and diversity. Multiple male and female genes that interact with Sex Peptide exhibited elevated FST x pi values. Genome-wide analyses also revealed an enrichment of genes critical for neuronal development, pointing to courtship evolution. Specifically, fruitless, its interacting genes, and a female behavior gene were identified as outliers. These parallel findings indicate that both sperm competition and mating behaviors are subject to co-evolutionary selection.

evolutionary biology↗

How Fisherian runaway halts: Genomic architecture determines the long-term evolutionary consequences of sexual selection.

Sexual selection explains the evolution of exaggerated sexual displays, but less obvious is why biased mate preferences--a requirement for sexual selection--evolve. Fisher (1930) proposed that biased mate preferences can spark self-reinforcing evolutionary process (runaway) that drives their own evolution. This occurs because mate choice imposes sexual selection on sexual displays and links them genetically to mate preferences, producing indirect selection on the preferences themselves. While mathematical models have demonstrated the plausibility of the runaway theory, they rely on several idealized assumptions. Consequently, it remains poorly understood how runaway halts once populations deviate from these idealized conditions as a consequence of evolution via runaway, and how the genetic architecture underlying sexual displays influences the resulting evolutionary dynamics. Here, we address these gaps using two complementary approaches. First, we review and synthesize existing theories to classify the mechanisms that halt runaway into four categories, based on which idealized assumptions of Lande's (1981) classic model are violated during evolution via runaway. Second, we conduct individual-based evolutionary simulations varying the genetic architecture of sexual displays from conventional additive to omnigenic inheritance models. Our results show that genetic architecture determines how runaway process halts, thereby governing long-term evolutionary dynamics under sexual selection.

evolutionary biology↗