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Duplicability of self-interacting human genes
Asa Pérez-Bercoff1, Takashi Makino, Aoife McLysaght
1Smurfit Institute of Genetics, University of Dublin, Trinity College, Dublin 2, Ireland.
BMC Evolutionary Biology
|June 1, 2010
Summary
Genes encoding self-interacting proteins show higher duplicability, often arising from whole-genome duplication events. This suggests gene duplication plays a key role in the evolution of protein interactions and functions.
Area of Science:
- Evolutionary biology
- Genomics
- Proteomics
Background:
- Protein-protein interactions are crucial for cellular functions and their evolution informs the development of new protein functions.
- A leading model suggests new interactions and complexes evolve via duplication of self-interacting genes, supported by yeast data.
- The human genome's gene duplication and self-interaction patterns were investigated.
Purpose of the Study:
- To examine the relationship between gene duplication and protein self-interaction in the human genome.
- To determine if self-interacting genes exhibit higher duplicability compared to non-self-interacting genes.
- To compare duplication mechanisms (whole-genome vs. small-scale) for self-interacting proteins.
Main Methods:
- Analyzed 34,808 interactions from 8,881 human genes.
- Assessed gene duplicability based on self-interaction status.
- Compared self-interaction prevalence in genes duplicated via whole-genome duplication (WGD) versus small-scale duplication (SSD).
- Controlled for gene age to interpret interaction patterns.
Main Results:
- Self-interacting proteins are encoded by genes with significantly higher duplicability.
- This finding remained robust across different methods for defining duplicate genes.
- Genes duplicated via WGD showed a general tendency for more interactions compared to SSD genes.
- The increased interactions in WGD genes were linked to their greater age.
Conclusions:
- Genes encoding self-interacting proteins possess higher duplicability.
- Duplicate genes for self-interacting proteins more frequently originate from WGD than SSD.
- Self-interacting WGD genes have more interaction partners, attributable to their older age.
- Contextual factors significantly influence gene duplicability.
Related Concept Videos
Gene Duplication and Divergence
The seminal work of Ohno in 1970 popularized the idea of gene duplication and divergence. DNA sequence comparison studies reveal that a large portion of the genes in bacteria, archaebacteria, and eukaryotes was generated by gene duplication and divergence, indicating its critical role in evolution.
The duplicated copies of the gene are called Paralogs. Paralogs with similar sequences and functions form a gene family. Across several species, a large number of gene families are characterized.
The duplicated copies of the gene are called Paralogs. Paralogs with similar sequences and functions form a gene family. Across several species, a large number of gene families are characterized.
Gene Families
Gene families consist of groups of genes proposed to have originated from a common ancestor. Typically these arise through events in which a gene or genes are mistakenly duplicated during cell division. Unlike their parent genes (which are subject to selection pressure to maintain function), these gene copies do not need to preserve their sequences and may evolve at a relatively faster rate.
Occasionally these regions can be adapted to take on new roles within the organism, becoming novel genes...
Occasionally these regions can be adapted to take on new roles within the organism, becoming novel genes...
Genome Copying Errors
DNA replication is a well-evolved process that copies millions of base pairs with high fidelity during each cell division. Occasionally a wrong base or a long stretch of wrong bases may get added to the daughter strands. If the errors are left unchecked, cells might accumulate several mutations that might endanger their survival. Therefore, the copying errors are checked and repaired at three levels.
Gene Conversion
Other than maintaining genome stability via DNA repair, homologous recombination plays an important role in diversifying the genome. In fact, the recombination of sequences forms the molecular basis of genomic evolution. Random and non-random permutations of genomic sequences create a library of new amalgamated sequences. These newly formed genomes can determine the fitness and survival of cells. In bacteria, homologous and non-homologous types of recombination lead to the evolution of new...
Gene Conversion
Other than maintaining genome stability via DNA repair, homologous recombination plays an important role in diversifying the genome. In fact, the recombination of sequences forms the molecular basis of genomic evolution. Random and non-random permutations of genomic sequences create a library of new amalgamated sequences. These newly formed genomes can determine the fitness and survival of cells. In bacteria, homologous and non-homologous types of recombination lead to the evolution of new...
Genome Size and the Evolution of New Genes
While every living organism has a genome of some kind (be it RNA, or DNA), there is considerable variation in the sizes of these blueprints. One major factor that impacts genome size is whether the organism is prokaryotic or eukaryotic. In prokaryotes, the genome contains little to no non-coding sequence, such that genes are tightly clustered in groups or operons sequentially along the chromosome. Conversely, the genes in eukaryotes are punctuated by long stretches of non-coding sequence.

