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Evolutionary origins of Brassicaceae specific genes in Arabidopsis thaliana.

Donoghue MT, Keshavaiah C, Swamidatta SH, Spillane C - BMC Evol. Biol. (2011)

Bottom Line: Over half of the subset of the 958 lineage-specific genes found only in Arabidopsis thaliana have alignments to intergenic regions in Arabidopsis lyrata, consistent with either de novo origination or differential gene loss and retention, with both evolutionary scenarios explaining the lineage-specific status of these genes.This study comprehensively identifies all of the Brassicaceae-specific genes in Arabidopsis thaliana and identifies how the majority of such lineage-specific genes have arisen.Insights regarding the functional roles of lineage-specific genes are further advanced through identification of enrichment for stress responsiveness in lineage-specific genes, highlighting their likely importance for environmental adaptation strategies.

View Article: PubMed Central - HTML - PubMed

Affiliation: Department of Biochemistry, University College Cork, Cork, Ireland.

ABSTRACT

Background: All sequenced genomes contain a proportion of lineage-specific genes, which exhibit no sequence similarity to any genes outside the lineage. Despite their prevalence, the origins and functions of most lineage-specific genes remain largely unknown. As more genomes are sequenced opportunities for understanding evolutionary origins and functions of lineage-specific genes are increasing.

Results: This study provides a comprehensive analysis of the origins of lineage-specific genes (LSGs) in Arabidopsis thaliana that are restricted to the Brassicaceae family. In this study, lineage-specific genes within the nuclear (1761 genes) and mitochondrial (28 genes) genomes are identified. The evolutionary origins of two thirds of the lineage-specific genes within the Arabidopsis thaliana genome are also identified. Almost a quarter of lineage-specific genes originate from non-lineage-specific paralogs, while the origins of ~10% of lineage-specific genes are partly derived from DNA exapted from transposable elements (twice the proportion observed for non-lineage-specific genes). Lineage-specific genes are also enriched in genes that have overlapping CDS, which is consistent with such novel genes arising from overprinting. Over half of the subset of the 958 lineage-specific genes found only in Arabidopsis thaliana have alignments to intergenic regions in Arabidopsis lyrata, consistent with either de novo origination or differential gene loss and retention, with both evolutionary scenarios explaining the lineage-specific status of these genes. A smaller number of lineage-specific genes with an incomplete open reading frame across different Arabidopsis thaliana accessions are further identified as accession-specific genes, most likely of recent origin in Arabidopsis thaliana. Putative de novo origination for two of the Arabidopsis thaliana-only genes is identified via additional sequencing across accessions of Arabidopsis thaliana and closely related sister species lineages. We demonstrate that lineage-specific genes have high tissue specificity and low expression levels across multiple tissues and developmental stages. Finally, stress responsiveness is identified as a distinct feature of Brassicaceae-specific genes; where these LSGs are enriched for genes responsive to a wide range of abiotic stresses.

Conclusion: Improving our understanding of the origins of lineage-specific genes is key to gaining insights regarding how novel genes can arise and acquire functionality in different lineages. This study comprehensively identifies all of the Brassicaceae-specific genes in Arabidopsis thaliana and identifies how the majority of such lineage-specific genes have arisen. The analysis allows the relative importance (and prevalence) of different evolutionary routes to the genesis of novel ORFs within lineages to be assessed. Insights regarding the functional roles of lineage-specific genes are further advanced through identification of enrichment for stress responsiveness in lineage-specific genes, highlighting their likely importance for environmental adaptation strategies.

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Summary of the origins of stress responsive LSGs.
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Figure 6: Summary of the origins of stress responsive LSGs.

Mentions: In comparison to the evolutionary origins of LSGs in general, the stress responsive genes have a larger proportion of LSGs with unknown origins, with 30.48% and 49.64% for all LSGs and stress responsive LSGs respectively. In contrast, the stress responsive LSGs have a smaller proportion of LSGs with Arabidopsis lyrata out-of-frame or intergenic hits, 29.85% for all LSGs and 12.41% for stress responsive LSGs (Figure 6). The increased proportion of Brassicaceae-specific LSGs without identifiable origins could be suggestive of an increased rate of evolution at some time during the evolution of these genes, and indeed the stress responsive LSGs do display increased dN/dS values as observed in LSGs generally (Additional file 3). Furthermore, in contrast to the broader set of Brassicaceae LSGs, the lower incidence of stress responsive Arabidopsis thaliana-only LSGs suggests that a greater proportion of Brassicaceae-only stress responsive LSGs have been established before the divergence between Arabidopsis thaliana and Arabidopsis lyrata.


Evolutionary origins of Brassicaceae specific genes in Arabidopsis thaliana.

Donoghue MT, Keshavaiah C, Swamidatta SH, Spillane C - BMC Evol. Biol. (2011)

Summary of the origins of stress responsive LSGs.
© Copyright Policy - open-access
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC3049755&req=5

Figure 6: Summary of the origins of stress responsive LSGs.
Mentions: In comparison to the evolutionary origins of LSGs in general, the stress responsive genes have a larger proportion of LSGs with unknown origins, with 30.48% and 49.64% for all LSGs and stress responsive LSGs respectively. In contrast, the stress responsive LSGs have a smaller proportion of LSGs with Arabidopsis lyrata out-of-frame or intergenic hits, 29.85% for all LSGs and 12.41% for stress responsive LSGs (Figure 6). The increased proportion of Brassicaceae-specific LSGs without identifiable origins could be suggestive of an increased rate of evolution at some time during the evolution of these genes, and indeed the stress responsive LSGs do display increased dN/dS values as observed in LSGs generally (Additional file 3). Furthermore, in contrast to the broader set of Brassicaceae LSGs, the lower incidence of stress responsive Arabidopsis thaliana-only LSGs suggests that a greater proportion of Brassicaceae-only stress responsive LSGs have been established before the divergence between Arabidopsis thaliana and Arabidopsis lyrata.

Bottom Line: Over half of the subset of the 958 lineage-specific genes found only in Arabidopsis thaliana have alignments to intergenic regions in Arabidopsis lyrata, consistent with either de novo origination or differential gene loss and retention, with both evolutionary scenarios explaining the lineage-specific status of these genes.This study comprehensively identifies all of the Brassicaceae-specific genes in Arabidopsis thaliana and identifies how the majority of such lineage-specific genes have arisen.Insights regarding the functional roles of lineage-specific genes are further advanced through identification of enrichment for stress responsiveness in lineage-specific genes, highlighting their likely importance for environmental adaptation strategies.

View Article: PubMed Central - HTML - PubMed

Affiliation: Department of Biochemistry, University College Cork, Cork, Ireland.

ABSTRACT

Background: All sequenced genomes contain a proportion of lineage-specific genes, which exhibit no sequence similarity to any genes outside the lineage. Despite their prevalence, the origins and functions of most lineage-specific genes remain largely unknown. As more genomes are sequenced opportunities for understanding evolutionary origins and functions of lineage-specific genes are increasing.

Results: This study provides a comprehensive analysis of the origins of lineage-specific genes (LSGs) in Arabidopsis thaliana that are restricted to the Brassicaceae family. In this study, lineage-specific genes within the nuclear (1761 genes) and mitochondrial (28 genes) genomes are identified. The evolutionary origins of two thirds of the lineage-specific genes within the Arabidopsis thaliana genome are also identified. Almost a quarter of lineage-specific genes originate from non-lineage-specific paralogs, while the origins of ~10% of lineage-specific genes are partly derived from DNA exapted from transposable elements (twice the proportion observed for non-lineage-specific genes). Lineage-specific genes are also enriched in genes that have overlapping CDS, which is consistent with such novel genes arising from overprinting. Over half of the subset of the 958 lineage-specific genes found only in Arabidopsis thaliana have alignments to intergenic regions in Arabidopsis lyrata, consistent with either de novo origination or differential gene loss and retention, with both evolutionary scenarios explaining the lineage-specific status of these genes. A smaller number of lineage-specific genes with an incomplete open reading frame across different Arabidopsis thaliana accessions are further identified as accession-specific genes, most likely of recent origin in Arabidopsis thaliana. Putative de novo origination for two of the Arabidopsis thaliana-only genes is identified via additional sequencing across accessions of Arabidopsis thaliana and closely related sister species lineages. We demonstrate that lineage-specific genes have high tissue specificity and low expression levels across multiple tissues and developmental stages. Finally, stress responsiveness is identified as a distinct feature of Brassicaceae-specific genes; where these LSGs are enriched for genes responsive to a wide range of abiotic stresses.

Conclusion: Improving our understanding of the origins of lineage-specific genes is key to gaining insights regarding how novel genes can arise and acquire functionality in different lineages. This study comprehensively identifies all of the Brassicaceae-specific genes in Arabidopsis thaliana and identifies how the majority of such lineage-specific genes have arisen. The analysis allows the relative importance (and prevalence) of different evolutionary routes to the genesis of novel ORFs within lineages to be assessed. Insights regarding the functional roles of lineage-specific genes are further advanced through identification of enrichment for stress responsiveness in lineage-specific genes, highlighting their likely importance for environmental adaptation strategies.

Show MeSH
Related in: MedlinePlus