Research Paper Advance Articles
Genetic variation between long-lived versus short-lived bats illuminates the molecular signatures of longevity
- 1 School of Biology and Environmental Science, University College Dublin, Belfield, Ireland
- 2 Department of Migration, Max Planck Institute of Animal Behavior, Radolfzell, Germany
- 3 Department of Biology, University of Konstanz, Konstanz, Germany
- 4 Smithsonian Tropical Research Institute, Panama
Received: June 6, 2020 Accepted: July 6, 2020 Published: July 16, 2020https://doi.org/10.18632/aging.103725
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Copyright © 2020 Huang et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Bats are the longest-lived mammals given their body size with majority of species exhibiting exceptional longevity. However, there are some short-lived species that do not exhibit extended lifespans. Here we conducted a comparative genomic and transcriptomic study on long-lived Myotis myotis (maximum lifespan = 37.1 years) and short-lived Molossus molossus (maximum lifespan = 5.6 years) to ascertain the genetic difference underlying their divergent longevities. Genome-wide selection tests on 12,467 single-copy genes between M. myotis and M. molossus revealed only three genes (CCDC175, FATE1 and MLKL) that exhibited significant positive selection. Although 97.96% of 12,467 genes underwent purifying selection, we observed a significant heterogeneity in their expression patterns. Using a linear mixed model, we obtained expression of 2,086 genes that may truly represent the genetic difference between M. myotis and M. molossus. Expression analysis indicated that long-lived M. myotis exhibited a transcriptomic profile of enhanced DNA repair and autophagy pathways, compared to M. molossus. Further investigation of the longevity-associated genes suggested that long-lived M. myotis have naturally evolved a diminished anti-longevity transcriptomic profile. Together with observations from other long-lived species, our results suggest that heightened DNA repair and autophagy activity may represent a universal mechanism to achieve longevity in long-lived mammals.
Natural selection has shaped a large variation of lifespan across mammals, with maximum lifespan ranging from a few months (e.g. short-lived shrews) to 211 years (e.g. bowhead whale) . Although the bowhead whale is exceptionally long-lived, its lifespan is arguably not as extreme as that of a 30 years old naked mole-rat given their body sizes, as maximum lifespan (MLS) exhibits a positive correlation with body size within mammals [2, 3]. Thus, lifespan comparison across mammals requires body size correction. To resolve this, the longevity quotient (LQ) was introduced, which is defined as the ratio of observed lifespan to predicted lifespan for a non-flying mammal of the same body size [2, 3]. Using this approach bats are the longevity extremists, with some species living up to ten times longer than expected given their body size . The Brandt’s bat (Myotis brandtii) holds the record for longevity , with a maximum lifespan of >40 years, living 8~10 times longer than expected given body size (~7 grams) [2, 4, 5]. This renders bats as one of the most ideal taxa to explore the molecular basis of extraordinary longevity in mammals.
Although the majority of bat species are long-lived, especially within the Myotis genus, there are a few short-lived exceptions, such as the velvety free-tailed bat (Molossus molossus) and the evening bat (Nycticeius humeralis), living as long as would be expected given their body size [5, 6]. A recent study has suggested that the ancestral bat lived up to 2.6 times longer than expected given body size, indicating that the extreme longevity observed in the longest-lived bat genera may have evolved multiple times . This also suggests that short-lived bat species may have lost their longevity adaptations. Therefore, this wide range of lifespans observed in bats enables us to utilize comparative evolutionary approaches to search for genetic differences within closely-related long- and short-lived bat species. In contrast to comparative studies on phylogenetically-distant species (e.g. bats versus mice), this comparison could minimize the ‘noise’ resulting from heterogenous physiology, and may reveal key anti-aging molecular adaptations that have evolved in long-lived bats, or were lost in their short-lived counterparts.
Genome-wide comparative analyses have been carried out on a few long- and short-lived species in primates , rodents [9, 10], whales  and bats . These studies revealed a few genes that showed convergent amino acid mutations, or exhibited positive selection, or were differentially expressed in long-lived species compared with their short-lived counterparts. Although there is little commonality across the gene candidates that are associated with longevity revealed by these studies, they are mainly enriched in DNA repair and maintenance, autophagy, homeostasis, and nutrient sensing pathways . In bats, our previous longitudinal studies showed that long-lived M. myotis bats maintained their transcriptomic profiles  and telomere length , and did not exhibit an increased level of mitochondrial damage with advancing age , all of which likely contribute to their extraordinary longevity. However, a parallel comparison between long- and short-lived bats is lacking.
In this study we performed a comparative genomic and transcriptomic analysis between long-lived Myotis myotis (MLS = 37.1 years; LQ = 5.71) and short-lived Molossus molossus (MLS = 5.6 years; LQ = 0.99)  to ascertain the molecular signatures associated with longevity in bats. Based on the genome-wide alignments of single-copy orthologous genes between these two species, we detected and further investigated the genes that were fast-evolving and showed significant positive selection. We also deep sequenced blood transcriptomes from eight adult individuals for each species, and explored the genes and pathways that were differentially expressed. To ascertain if long-lived bats have evolved a transcriptomic signature of longevity, we further investigated the expression of ‘pro’- and ‘anti’-longevity genes in the blood transcriptomes of M. myotis and M. molossus. Although the majority of genes underwent purifying selection, we observed a significant transcriptional alteration between these two species. Among 2,086 genes that exhibited large interspecific expression variation, the genes that showed higher expression in long-lived M. myotis were mainly enriched in DNA repair and autophagy. Further pathway analysis suggested that six biological processes, including autophagy, were differentially expressed between M. myotis and M. molossus. We also show that M. myotis had significantly lower expression levels of anti-longevity genes, suggestive of a transcriptomic signature of longevity naturally evolved in long-lived bats. Together with the previous findings in other long-lived mammals, our study implies that enhanced DNA repair and autophagy activity may represent a universal mechanism to achieve longevity in long-lived mammals.
The majority of genes undergo purifying selection
To evaluate the natural selection acting on protein-coding genes between M. myotis and M. molossus, we calculated the ratio of Ka and Ks substitution rates for each pair of orthologous genes. We observed that most of the genes (97.96%) were under purifying selection (Ka/Ks ratio < 1, FDR < 0.05), with the median of Ka/Ks ratios equal to 0.103 (Figure 1A). In total, 48 genes had the ratios of Ka/Ks > 1, only three of which (FATE1, MLKL and CCDC175) exhibited significant positive selection (Fisher’s exact test, FDR < 0.05, Figure 1B). To determine if positive selection on these genes was the consequence of species-specific selective pressures, we conducted pairwise analyses of orthologous genes across 6 bat species (See Methods). We found that each comparison resulted in a unique set of positively selected genes (PSGs) (Supplementary Table 1). Interestingly, positive selection on FATE1 and CCDC175 was also observed between M. molossus, M. myotis and other bat species (Supplementary Table 1). Although MLKL was solely seen under significant positive selection between M. myotis and M. molossus, this gene also showed high Ka/Ks ratios between all possible comparisons of bat species (Figure 1C and 1D).
Figure 1. Analysis of Ka/Ks substitution rates of 12,467 single-copy genes between M. myotis and M. molossus. (A) Distribution of Ka/Ks ratios of 12,467 single-copy genes. To better visualize the distribution, six genes with Ka/Ks > 1.5 were not included in this plot. (B) Genes with Ka/Ks > 1. Three genes highlighted in red show significant positive selection (Ka/Ks > 1; FDR < 0.05 Fisher’s exact test). (C) Significance (FDR) of Ka/Ks ratios of FATE1, CCDC175 and MLKL between 6 bat species through pairwise comparisons. The red values indicate significant positive selection while the blue values indicate significant purifying selection. The black values indicate no selection. (D) Ka/Ks ratios of FATE1, CCDC175 and MLKL between 6 bat species through pairwise comparisons. The red values indicate Ka/Ks ratios > 1 while the blue values indicate Ka/Ks ratios < 1.
Transcriptomic profiles exhibit a substantial difference in long-lived and short-lived bats
To ascertain the differences on the transcriptional level, we further sequenced and compared their blood transcriptomes (n = 16) using Illumina RNA-Seq. Out of 12,467 orthologs, we excluded 1,832 genes that were not expressed in either M. molossus or M. myotis and retained 10,635 genes for downstream analyses. The correlation analysis revealed a considerable difference in global transcriptomic profiles between M. molossus and M. myotis (Figure 2A, See Methods). The samples showed statistically higher intraspecific Spearman’s correlation coefficients (ρ = 0.957) in contrast to the interspecific counterparts (ρ = 0.766) (P = 2.2×10-16, Wilcoxon signed-rank test). In addition, 4,846 (45.57%) genes were differentially expressed (FDR < 0.05). 2,162 (20.33%) genes showed up-regulation in M. myotis compared to M. molossus while 2,684 (25.24%) genes were down-regulated (Figure 2B). Interestingly, there was no significant difference in the distribution of Ka/Ks ratios between differentially and non-differentially expressed genes (P = 0.162, Kolmogorov-Smirnov test). Next, we tested if the Ka/Ks ratios of 10,635 orthologs had an association with their differential expression patterns in M. molossus and M. myotis. We found that there was no significant association between the genes differentially expressed and their Ka/Ks ratios (P = 0.352, χ2 test, See Methods).
Figure 2. Comparisons of M. myotis and M. molossus blood transcriptomes. (A) Spearman’s correlation coefficients between M. myotis and M. molossus blood transcriptomes based on expression levels of 10,635 single-copy genes. We excluded 1,832 genes that were neither expressed in M. myotis nor M. molossus. (B) Differential gene expression analysis between M. myotis and M. molossus blood transcriptomes. Genes with FDR < 0.05 were considered differentially expressed genes (DEGs).
DNA repair and autophagy are enriched by the genes that have genetically higher expression in long-lived bats
For each of 10,635 genes, we calculated the proportion of interspecific expression variation using a linear mixed model (See Methods). On average, 24.9% of gene expression variance was explained by ‘species’ while ‘sex’ only explained a small proportion of variation (Figure 3A). To investigate the gene expression that genetically differed in M. myotis and M. molossus, we focused on 2,086 genes with at least 80% of their expression variance resulted from ‘species’ which represented interspecific variation (See Methods). As was expected, 2,083 of these genes (99.86%) were also detected as differentially expressed genes (DEGs) (Figure 3B).
Figure 3. Gene expression variation analysis. (A) Evaluation of gene expression variance using a linear mixed model. Residual variance represents the contribution from uncharacterized variables. (B) Overlap of differentially expressed genes (blue) and the genes with at least 80% of expression variation resulted from ‘species’ (grey). (C) GO terms that were enriched by 1,060 genes that had higher expression in M. molossus. (D) GO terms that were enriched by 1,026 genes that had higher expression in M. myotis.
In total, 1,060 genes had higher expression levels in M. molossus while 1,026 genes in M. myotis. GO terms that were enriched for the genes with higher expression in short-lived bats include glycerolipid metabolic process, G1/S transition of mitotic cell cycle and RNA 3’-end processing (Figure 3C). In contrast, the genes that had higher expression in long-lived bats were enriched in a variety of biological processes such as RNA localization, viral life cycle and peptide biosynthetic process (Figure 3D). Interestingly, we observed that DNA repair and macroautophagy were also enriched for the genes that exhibited higher expression in long-lived bats (Figure 3D).
Pathway analysis reveals up-regulated autophagy pathways in long-lived bats
To identify the biological processes that were differentially expressed between short-lived and long-lived bats, we investigated the 20 GO terms that were enriched by these 2,086 genes. We compared expression levels of all the genes under each enriched GO term between M. myotis and M. molossus using Wilcoxon signed-rank test (paired mode, one-tailed test) (See Methods). Out of these 20 terms, the genes under 6 terms had significantly higher expression in long-lived bats than in short-lived bats (FDR < 0.05) (Figure 4A). These GO terms include DNA geometric change (GO:0032392), RNA localization (GO:0006403), autophagy (GO:0006914), nucleobase-containing compound catabolic process (GO:0034655), plasma membrane bounded cell projection assembly (GO:0120031), and organelle localization (GO:0051640) (Figure 4B). In contrast, none of these 20 GO terms exhibited significantly higher expression in M. molossus than in M. myotis, respectively (Wilcoxon signed-rank test, paired mode, one-tailed, FDR < 0.05). The genes under each of these 20 enriched GO terms are available in Supplementary Table 2.
Figure 4. Expression analysis of the 20 GO terms between M. myotis and M. molossus. (A) Differential expression analysis of GO terms enriched by 2,086 genes that showed >80% interspecific expression variation. Differentially expressed GO terms were determined by comparing gene expression under each GO term using Wilcoxon signed-rank test (paired mode; one-tailed test). GO terms with FDR < 0.05 were considered differentially expressed. (B) Distribution of gene expression under each of 6 differentially expressed GO terms between M. myotis and M. molossus.
Long-lived bats have evolved a transcriptomic signature of longevity
To ascertain whether long-lived bats have naturally evolved a transcriptomic signature of longevity, we compiled a list of anti-longevity and pro-longevity genes and compared their expression in the M. myotis and M. molossus blood transcriptomes. We observed that there was no significant difference in the expression of the pro-longevity genes (n = 28) in long-lived and short-lived bats (P = 0.381, Wilcoxon signed-rank test, paired mode, one-tailed, Figure 5A), while the anti-longevity genes (n=19) had significantly lower expression in long-lived bats (P = 0.0364, Wilcoxon signed-rank test, paired mode, one-tailed, Figure 5B). To assess its significance, we randomly subsampled 19 genes out of 2,086 genes for 1,000 times, and performed Wilcoxon signed-rank tests as stated above and analysed the distribution of the P-values. We noticed that P = 0.0364 fell outside the range of 95% highest density interval (lower: 0.0844, upper: 0.998), suggesting that the significance of the test did not result from random chance.
Figure 5. Expression analysis of anti- and pro-longevity genes between M. myotis and M. molossus. (A) Comparison of anti-longevity gene expression (n = 19) between M. myotis and M. molossus using Wilcoxon signed-rank test (paired mode, one-tailed test). (B) Comparison of pro-longevity gene expression (n = 28) between M. myotis and M. molossus using Wilcoxon signed-rank test (paired mode, one-tailed test).
Identifying positive selection is a powerful approach to detect genomic adaptations that may contribute to species-specific phenotypes. In this study, we aimed to identify signatures of positive selection within a short-lived bat species (Molossus molossus) and a longer-lived bat species (Myotis myotis) to reveal genomic adaptations that correlate with longevity. Similar to previous studies examining positive selection in bat lineages [16, 17], the majority of genes investigated in this study were under purifying selection, which is not surprising given the evolutionary constraint on protein-coding genes. However, signs of significant positive selection were detected in 3 genes (FATE1, MLKL and CCDC175) between M. molossus and M. myotis, two of which (FATE1 and CCDC175) were also under significant positive selection among other bat species (Supplementary Table 1). This suggests that FATE1 and CCDC175 evolved fast along all bat lineages examined and their positive selection might not be associated with longevity. We noticed that MLKL was uniquely seen under significant positive selection between M. molossus and M. myotis (Figure 1C). MLKL is a key signaling molecule in the necroptosis pathway, a programmed cell death process , and deregulation of this gene has been reported to promote necroptosis-induced inflammation in aged mice . Interestingly, a recent study investigating several long- and short-lived rodents revealed a different set of PSGs, which were enriched in cellular homeostasis and mTOR pathway . The disparity of PSGs may result from different taxa and methods used in these two studies or suggest that the longevity mechanisms evolved in long-lived mammals are species-specific. In our study, we only examined two bat lineages that have extremely divergent lifespans. As more and more high-quality bat genomes will become available , a more powerful and comprehensive investigation, such as applying branch-site tests for positive selection to multiple long- and short-lived branches, is required.
Although we did not observe strong signals of positive selection on these protein-coding genes, we did notice a significant difference in their expression between M. myotis and M. molossus. Interestingly, we showed that differential or non-differential expression of these genes had no association with the selective pressures acting on them (P = 0.352, χ2 test). Only one of the three PSGs (FATE1) found in our study was differentially expressed. Therefore, we hypothesize that differential gene expression is likely due to post-transcriptional regulation of non-coding genes rather than natural selection on these protein-coding genes .
Differential expression analysis measures the difference in mean expression of genes between these two species but fails to uncover the intraspecific gene expression variation . Transcriptomes are subjected to change due to instant alterations of physiological status or environmental context. As the biometrics of M. myotis and M. molossus individuals used in this study, such as age, disease status and environmental circumstances, are unknown, a large proportion of intraspecific transcriptional variation is expected. One purpose of this study is to identify gene expression that genetically differs in these two species; hence we need to explore the genes which have high interspecific but low intraspecific expression variation. To resolve this, we employed a linear mixed model to quantify gene expression variation (See Methods). We focused on 2,086 genes with at least 80% of their overall expression variance resulted from interspecific difference, and indeed, a huge overlap between these genes and DEGs was revealed (Figure 3B). We excluded 2,763 DEGs with large proportions of intraspecific and other unknown variation from further analyses, as their differential expression might not reflect genetic difference between these two species.
Among these 2,086 genes, we noticed that the genes having higher expression in long-lived M. myotis were enriched in DNA repair and autophagy. For example, WRN and XPC were expressed 6.7-fold and 4.8-fold higher in M. myotis compared to M. molossus, respectively. WRN has been shown to regulate the repair of DNA double strand breaks (DSBs) and may play a role in telomere maintenance , while XPC may act as a general sensor of damaged DNA and involve in base excision repair (BER) . Genomic stability is under constant challenge by intrinsic and extrinsic agents . In most mammals, the capability of genomic maintenance attenuates with advancing age, leading to accumulation of DNA damage and thus, age-related phenotypes [26, 27]. However, together with our previous findings in long-lived M. myotis bats , multiple lines of evidence have revealed up-regulation of genes directly involved in DNA damage signalling and repair in a few long-lived mammals during aging, such as human , naked mole-rat  and bowhead whale . In addition, autophagy is a critical recycling pathway which maintains cellular metabolism and energy homeostasis [29, 30]. We found that UVRAG, which was identified as a tumor suppressor, was up-regulated 13.7-fold in long-lived M. myotis compared to M. molossus. UVRAG induces autophagosome formation and maturation, and its overexpression promotes autophagy and suppress tumor cell growth . Other autophagy-related genes (e.g. ATG3, ATG4A, ATG4C) also exhibited significantly higher expression in M. myotis. Increased autophagy activity may allow long-lived M. myotis to better counteract the age-related accumulation of damaged proteins and organelles, thus to improve the metabolic fitness of cells. Consistent with our finding, recent studies on rodents  and whales  show that autophagy is significantly enhanced in long-lived species relative to their short-lived counterparts. These results imply that enhanced DNA repair and autophagy activity may represent a universal mechanism to achieve longevity in long-lived species, independent of their phylogenetic distance. Interesting, we also found that the genes enriched in ‘Viral life cycle’ had significantly higher expression in M. myotis (Figure 3D). This may be due to the possibility that the M. myotis individuals, sampled from the colonies in France, carried a higher viral load or could represent naturally evolved anti-viral mechanism in long-lived bats. This may result in activation of the genes that control viral replication in M. myotis. Coupled with some other enriched GO terms (e.g. RNA localization, glycerolipid metabolic process and mitotic cell cycle phase transition), its roles in the aging process in bats will need further exploration.
Focusing on these 2,086 genes, we further explored the biological processes and expression of all the genes that were enriched under each GO term (See Methods). We found that, compared to M. molossus, the genes under 6 enriched GO categories had significantly higher expression in M. myotis, respectively (Figure 4A and 4B, Wilcoxon signed-rank test, FDR-adjusted P < 0.05). Apart from autophagy which has a crucial role in the regulation of lifespan, the other 5 terms have not been clearly linked with aging yet. These 5 differentially expressed GO categories may indicate the general transcriptomic differences between these two species.
Next, we investigated a list of pro-longevity and anti-longevity genes  to ascertain if long-lived bats have naturally evolved a transcriptomic profile of longevity. These genes are mainly involved in DNA repair, immunity, and cell growth and proliferation, which have been functionally validated to shorten or prolong lifespan in mice via overexpression, knockdown or knockout experiments . Our results suggest that, while the expression levels of the pro-longevity genes did not significantly differ between these two species, M. myotis are likely to achieve longevity by suppressing the expression of some anti-longevity genes. Most remarkably, IGF1R and DGAT1 were down-regulated 23.7-fold and 23.2-fold in long-lived M. myotis compared to short-lived M. molossus, respectively. IGF1R is an insulin receptor which exerts pleiotropic roles in glucose metabolism, cell growth development and survival . However, deregulation of IGF1R expression, commonly seen within individuals in their late-life stage, is associated with the occurrence and development of diabetes, inflammation and cancer . It has been reported that igf1r-knockout mice live on average 26% longer than their wide-type littermates . In addition, a previous study observed decreased expression of genes involved in insulin/IGF-1 signalling pathways in the liver of naked mole-rat compared with mice . Likewise, the role of DGAT1 is diverse and its overexpression promotes the development of insulin resistance, obesity and fatty-acid induced inflammation [37, 38]. Deficiency of DGAT1 protects against the metabolic consequences of aging and extends mean and maximal lifespan in mice . These candidates, together with their expression patterns in long-lived bats, could present promising therapeutic targets to delay aging in humans. However, how M. myotis bats naturally regulate and control expression of these genes requires further investigation, particularly on non-coding regions that may underlie the regulatory mechanisms of their longevity adaptations .
In summary, comparative genomic and transcriptomic analyses on M. molossus and M. myotis resulted in the discovery of some genetic signatures that may underlie the exceptional longevity in long-lived bats. We show that, even though most of the genes are under purifying selection, long-lived M. myotis bats exhibit a different expression profile of enhanced DNA repair and autophagy pathways, and diminished anti-longevity genes, which likely contributes to their extraordinary long lifespan. In the future, selection tests on multiple pairs of phylogenetically matched long- and short-lived branches are required to address if long-lived bats exhibit convergent signatures of longevity or if each lineage has evolved its own longevity adaptations. In addition, longitudinal studies of bats within different LQs will need to be carried out to identify the age-associated genes and pathways that are differentiated between long- and short-lived bats. As the PSGs and DEGs are suggested on the basis of in silico analyses, in vitro functional assays are required to confirm their roles in bat longevity.
Materials and Methods
Genome-wide analysis of Ka/Ks substitution rates
To assess the selective pressure acting on protein-coding genes, we analysed genome-wide alignments of 12,467 single-copy orthologs between M. myotis and M. molossus. These alignments were obtained from the Bat1K project [12, 20]. For each pair of orthologs, we calculated the ratio of nonsynonymous (Ka) and synonymous (Ks) substitution rates using KaKs_Calculator (v2.0)  with the Model Averaging (MA) method. Model averaging weights each candidate model (7 in total) and engages more than one model to estimate average parameters across models. Fisher’s exact test was performed to determine the significance of positive selection. The genes with Ka/Ks >1 and adjusted P-value (FDR) < 0.05 were considered significant positive selection. We further inspected and filtered the positively selected genes (PSGs) due to short alignment (less than 100 bp) and low sequence coverage (less than 80%).
To ascertain if the PSGs identified are unique to the M. myotis and M. molossus comparison, we included 4 other bat species, which are equivalent in genome completeness and annotation (Pipistrellus kuhlii, Phyllostomus discolor, Rhinolophus ferrumequinum and Rousettus aegyptiacus), and investigated Ka/Ks ratios of genes via pairwise comparisons (n = 15). The alignments of single-copy orthologs across these six species were obtained from the Bat1K project [12, 20]. The method for Ka/Ks calculation and the criteria for defining PSGs were the same as stated above.
Blood sample collection and RNA sequencing
The sampling procedures were undertaken in accordance with the ethical guidelines and permits issued by ‘Arrêté’ by the Préfet du Morbihan and the Ministerio de Ambiente de Panamá. M. myotis and M. molossus individuals were captured in Brittany, France and Gamboa, Panama, respectively. The blood sampling procedures were extensively described in . Blood samples were collected in cryotubes (2 ml, Nalgene labware) and were immediately flash frozen in liquid nitrogen. All samples were further preserved at -150°C for long-term storage before total RNA extraction. Whole blood total RNA extraction was carried out following the manufacturer’s protocols (RNAzol@ BD kit, catalog no. RB192, Molecular Research Centre, Inc) with modifications as reported in . The samples with RIN scores > 8.0 and total RNA > 2 μg satisfied the criteria for RNA-Seq. In this study, 16 qualified RNA samples (8 each for M. myotis and M. molossus) were used for Illumina RNA-Seq library preparation. Prior to extraction, the RNA samples were purified by Turbo DNA-freeTM kit (catalog number AM1907, Ambion) to deplete residual DNA, and were further treated with Globin-Zero Gold rRNA Removal kit (Epicentre Illumina) to remove abundant rRNA and globin transcripts. RNA-Seq libraries were prepared using the Tru-Seq Stranded RNA Library Prep kit (Illumina), and further barcoded and sequenced on an Illumina HiSeq2500 sequencer to generate 125-bp paired-end reads. Sample details and statistics of the RNA-Seq libraries are available in Supplementary Table 3.
Comparative transcriptomic analyses
For each sample, raw reads were trimmed adaptors and low-quality regions (< Q25) using Cutadapt (v.1.14) . The filtered reads were subsequently quantified against the reference genes using Salmon (v0.9)  with the following parameters: -k 31, -ISF. -k indicates the length of seed while -ISF indicates a library of stranded-specific paired-end reads oriented towards each other. Here, we used 12,467 pairs of single-copy orthologs as references for expression analysis for respective species. The genes which were not expressed in either M. molossus or M. myotis were excluded from downstream analysis. Based on gene expression, we computed pairwise Spearman’s correlation coefficients across samples using the R package cor (v.3.6.0) . Prior to analysis, raw expression counts were normalized using TMM (Trimmed Mean of M-value) method and further log2-transformed. Next, differential gene expression analysis was performed using the R package DESeq2 . The genes with an FDR < 0.01 were considered differentially expressed genes (DEGs). In addition, we also investigated the distributions of the Ka/Ks ratios of differentially and non-differentially expressed genes using a Kolmogorov-Smirnov test. We further performed a χ2 test to ascertain if the PSGs between M. myotis and M. molossus correlated with the DEGs identified (P-value < 0.05 was considered significant).
Gene expression variation analysis
Differential gene expression analysis measures the difference in mean expression between two groups but does not quantify expression variation within each group. To detect gene expression which may truly represent genetic difference between M. myotis and M. molossus, we employed a linear mixed model (LMM) to identify genes with high interspecific but low intraspecific variation. Normalised gene expression values were considered as dependent variables, whereas ‘species’ and ‘sex’ were considered as explanatory variables and were modelled as random effects. The variance from uncharacterized sources was treated as residual variance. The LMM was implemented using the R package variancePartition . We focused on the genes for which at least 80% of their expression variation was explained by ‘species’. This resulted in 2,086 genes that were further categorized into two groups depending on their expression in M. myotis and M. molossus. Using Metascape , function enrichment analyses were performed on the genes that had higher expression levels in M. myotis and M. molossus, respectively. The GO terms with FDR < 0.05 were considered significantly enriched.
Differential expression of biological processes between M. myotis and M. molossus
To identify the biological processes (GO terms) that were differentially expressed between M. myotis and M. molossus, we investigated gene expression at the GO term level. To achieve this, we focused on the 2,086 genes that may truly represent the genetic difference between these two species, and performed a GO enrichment analysis using Metascape . The GO terms with FDR < 0.05 were considered significantly enriched terms. Subsequently, we collected all the genes under each enriched term in M. myotis and M. molossus, and compared their expression levels using Wilcoxon signed-rank tests (paired mode, one-tailed test). The significance of tests was adjusted by Benjamini-Hochberg FDR, and the GO terms with FDR < 0.05 were considered differentially expressed between M. myotis and M. molossus.
Expression of anti- and pro-longevity genes in M. myotis and M. molossus
To further investigate whether M. myotis harbored a transcriptomic signature of longevity relative to M. molossus, we compiled a list of anti-longevity genes (n = 19) and pro-longevity genes (n = 28) from GenAge . These genes have been validated to either shorten (anti-longevity) or extend (pro-longevity) lifespan in mice via overexpression, knockdown or knockout. We tested whether their expression significantly differed in these two species using Wilcoxon signed-rank tests (paired mode; one-tailed test), respectively. Our result showed that expression levels of the anti-longevity genes had significantly lower expression (P < 0.05) in long-lived M. myotis than short-lived M. molossus. To evaluate the significance of this test, we randomly subsampled 19 genes out of 2,086 genes and performed Wilcoxon signed-rank tests as previously described. This was repeated 1,000 times with the P-value of each test collected and their distribution further analysed using the R package HDInterval. The list of anti- and pro-longevity genes investigated in this study and their expression levels in M. myotis and M. molossus blood can be available in Supplementary Table 4.
E.C.T. and Z.H. devised this study. E.C.T., C.V.W., and Z.H. collected Myotis myotis samples. D.D. collected Molossus molossus samples. C.V.W., and Z.H. performed RNA extraction. Z.H. performed all the data analysis and wrote the first draft. All the authors edited and approved the manuscript.
We thank Dr. Graham Hughes for the suggestions on selection tests. We also thank the numerous volunteers and students from Bretagne Vivante and University College Dublin for their help in Myotis myotis sample collection and the owners/authorities for allowing access to the sites.
Conflicts of Interest
The authors declare that there are no conflicts of interest.
This study was funded by a European Research Council Research Grant (No. ERC-2012-StG311000), a UCD Wellcome Institutional Strategic Support Fund, financed jointly by University College Dublin and SFI-HRB-Wellcome Biomedical Research Partnership (No. 204844/Z/16/Z), and an Irish Research Council Consolidator Laureate Award to Emma. C. Teeling.
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