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Cited by 89

The DOI matches its Crossref record; 54 of the 54 references it cites were found in a registry or an index.

Dissecting the role of low-complexity regions in the evolution of vertebrate proteins

Radó-Trilla, Núria, Albà, MMar·2012·BMC Evolutionary Biology
DOI 10.1186/1471-2148-12-155PMC PMC3523016
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Abstract

BACKGROUND: Low-complexity regions (LCRs) in proteins are tracts that are highly enriched in one or a few amino acids. Given their high abundance, and their capacity to expand in relatively short periods of time through replication slippage, they can greatly contribute to increase protein sequence space and generate novel protein functions. However, little is known about the global impact of LCRs on protein evolution. RESULTS: We have traced back the evolutionary history of 2,802 LCRs from a large set of homologous protein families from H.sapiens, M.musculus, G.gallus, D.rerio and C.intestinalis. Transcriptional factors and other regulatory functions are overrepresented in proteins containing LCRs. We have found that the gain of novel LCRs is frequently associated with repeat expansion whereas the loss of LCRs is more often due to accumulation of amino acid substitutions as opposed to deletions. This dichotomy results in net protein sequence gain over time. We have detected a significant increase in the rate of accumulation of novel LCRs in the ancestral Amniota and mammalian branches, and a reduction in the chicken branch. Alanine and/or glycine-rich LCRs are overrepresented in recently emerged LCR sets from all branches, suggesting that their expansion is better tolerated than for other LCR types. LCRs enriched in positively charged amino acids show the contrary pattern, indicating an important effect of purifying selection in their maintenance. CONCLUSION: We have performed the first large-scale study on the evolutionary dynamics of LCRs in protein families. The study has shown that the composition of an LCR is an important determinant of its evolutionary pattern.

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Figure 1 Conservation of low-complexity regions (LCRs) in chordate homologous protein families. LCRs are indicated in red. Only the region of the alignment containing the LCR is shown. a) Example of conserved chordate LCR enriched in lysines. Corresponds to methionyl aminopeptidase 2 (Ensembl Protein Identifier ENSP00000325312 in humans). b) Example of mammalian-specific LCR enriched in alanines. Corresponds to alkylation repair 5 (Ensembl Protein Identifier ENSP00000261650 in humans).
Figure 1 Conservation of low-complexity regions (LCRs) in chordate homologous protein families. LCRs are indicated in red. Only the region of the alignment containing the LCR is shown. a) Example of conserved chordate LCR enriched in lysines. Corresponds to methionyl aminopeptidase 2 (Ensembl Protein Identifier ENSP00000325312 in humans). b) Example of mammalian-specific LCR enriched in alanines. Corresponds to alkylation repair 5 (Ensembl Protein Identifier ENSP00000261650 in humans).CC BY · PubMed Central
Figure 2 Relative abundance of low-complexity regions (LCRs) at different phylogenetic depths. The area of the circles is proportional to LCR relative frequencies. The number of LCRs at each branch is indicated. In black, data for all LCRs. In blue, data for LCRs enriched in positively charged amino acids (K and R). In red, data for LCRs enriched in alanine (A), glycine (G) or both. The LCR phylogenetic distribution of LCRs labeled in blue, and of LCRs labeled in red, deviated significantly from the expected one considering all LCRs (Fisher’s exact test p < 10-5).
Figure 2 Relative abundance of low-complexity regions (LCRs) at different phylogenetic depths. The area of the circles is proportional to LCR relative frequencies. The number of LCRs at each branch is indicated. In black, data for all LCRs. In blue, data for LCRs enriched in positively charged amino acids (K and R). In red, data for LCRs enriched in alanine (A), glycine (G) or both. The LCR phylogenetic distribution of LCRs labeled in blue, and of LCRs labeled in red, deviated significantly from the expected one considering all LCRs (Fisher’s exact test p < 10-5).CC BY · PubMed Central
Figure 3 Observed versus expected number of LCRs in the different branches leading to an extant organism. Data is shown for LCRs enriched in K or R (in blue) and in A, G or AG (in red). The observed distribution of LCRs labeled in blue deviated significantly from the expected one in all three cases (Fisher’s exact test p < 10-3). The observed distribution of LCRs labeled in red deviated significantly from the expected one for human LCRs (Fisher’s exact test p < 10-3).
Figure 3 Observed versus expected number of LCRs in the different branches leading to an extant organism. Data is shown for LCRs enriched in K or R (in blue) and in A, G or AG (in red). The observed distribution of LCRs labeled in blue deviated significantly from the expected one in all three cases (Fisher’s exact test p < 10-3). The observed distribution of LCRs labeled in red deviated significantly from the expected one for human LCRs (Fisher’s exact test p < 10-3).CC BY · PubMed Central
Figure 4 Dynamics of gain and loss of low-complexity regions (LCRs) in vertebrate homologous protein families. The LCRs gained in each branch correspond to LCRs observed at different phylogenetic depths. The LCRs lost are estimated from LCR phylogenetic distribution data (see Methods). Values in square brackets in internal nodes represent the estimated number of ancestral LCRs.
Figure 4 Dynamics of gain and loss of low-complexity regions (LCRs) in vertebrate homologous protein families. The LCRs gained in each branch correspond to LCRs observed at different phylogenetic depths. The LCRs lost are estimated from LCR phylogenetic distribution data (see Methods). Values in square brackets in internal nodes represent the estimated number of ancestral LCRs.CC BY · PubMed Central

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Metadata

Authors
Radó-Trilla, N., & Albà, M.
Venue
BMC Evolutionary Biology
Publisher
Springer Science and Business Media LLC
Published
2012
Volume
12
Issue
1
Pages
155
ISSN
1471-2148
DOI
10.1186/1471-2148-12-155
PMC
PMC3523016
Cited by
89
References
54
Language
en

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