Abstract

BackgroundProteins convey the majority of biochemical and cellular activities in organisms. Over the course of evolution, proteins undergo normal sequence mutations as well as large scale mutations involving domain duplication and/or domain shuffling. These events result in the generation of new proteins and protein families. Processes that affect proteome evolution drive species diversity and adaptation. Herein, change over the course of metazoan evolution, as defined by birth/death and duplication/deletion events within protein families and domains, was examined using the proteomes of 9 metazoan and two outgroup species.ResultsIn studying members of the three major metazoan groups, the vertebrates, arthropods, and nematodes, we found that the number of protein families increased at the majority of lineages over the course of metazoan evolution where the magnitude of these increases was greatest at the lineages leading to mammals. In contrast, the number of protein domains decreased at most lineages and at all terminal lineages. This resulted in a weak correlation between protein family birth and domain birth; however, the correlation between domain birth and domain member duplication was quite strong. These data suggest that domain birth and protein family birth occur via different mechanisms, and that domain shuffling plays a role in the formation of protein families. The ratio of protein family birth to protein domain birth (domain shuffling index) suggests that shuffling had a more demonstrable effect on protein families in nematodes and arthropods than in vertebrates. Through the contrast of high and low domain shuffling indices at the lineages of Trichinella spiralis and Gallus gallus, we propose a link between protein redundancy and evolutionary changes controlled by domain shuffling; however, the speed of adaptation among the different lineages was relatively invariant. Evaluating the functions of protein families that appeared or disappeared at the last common ancestors (LCAs) of the three metazoan clades supports a correlation with organism adaptation. Furthermore, bursts of new protein families and domains in the LCAs of metazoans and vertebrates are consistent with whole genome duplications.ConclusionMetazoan speciation and adaptation were explored by birth/death and duplication/deletion events among protein families and domains. Our results provide insights into protein evolution and its bearing on metazoan evolution.

Highlights

  • Proteins convey the majority of biochemical and cellular activities in organisms

  • The lineages leading to the Last Common Ancestor (LCA) of human and mouse tend to have higher numbers of new family births, but it is the Last common ancestor (LCA) of C. elegans and C. briggsae that has the highest number of family births

  • 932 families disappeared in T. spiralis compared with less than 460 in C. elegans or C. briggsae, 487 families in G. gallus, and less than 200 in H. sapiens or M. musculus

Read more

Summary

Introduction

Over the course of evolution, proteins undergo normal sequence mutations as well as large scale mutations involving domain duplication and/or domain shuffling. These events result in the generation of new proteins and protein families. Over the course of evolution, proteins undergo mutations, duplications, and domain shuffling [5], which can result in the generation of new proteins and protein families through natural selection. Mutation and domain shuffling together with other genetic events can create functional variation and in some cases completely alter protein function These changes subject proteins to natural selection and adaptation which in turn lead to the generation of new domains, proteins, protein families, and species. Identifying and characterizing protein families or domains unique to parasites, i.e. parasitic nematodes, can result in better disease treatment and control

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call