GAB-2015v6n6 - page 9

Genomics and Applied Biology 2015, Vol. 6, No. 6, 1-7
6
biased in olfactory receptors (OR) was expected.
Sus
scrofa
have the largest repertoire of functional OR
genes in mammals whose genome has been sequenced
to date (Nguyen et al., 2012), likely related to the
strong dependence on their sense of smell for foraging
especially in wild and in extensive production system.
For efficiency of foraging different feeds, high
flexibility of codon usage is thus justified. There are
about 1301 porcine OR genes, nearly a third are found
as copy number variable in pigs. Such large numbers
of genes are less conserved and might explain the low
CUB as reported in this study. These findings suggest
that the wide variety of environmental conditions
faced by pigs around the world have resulted in low
CUB for flexibility and high CNVs. This low CUB
could be because these genes are less conserved and
need to evolve fast to adapt to ever changing antigenic
determinants and artificially created environment for
immune and olfactory receptor genes respectively.
Cell apoptosis through fas ligand (Griffith et al., 1995)
being the principal mechanism by which the majority
of effecter T and B lymphocytes die after clearance of
an infection may justify the low CUB witnessed in this
study. This might be to meet the changing infection-
clearance status to regulate uncontrolled activation of
lymphocytes that may result to self-destruction, limit auto
reactivity and bring forth immune tolerance.
Conclusion
Functional analyses revealed high and low codon
usage bias enriched with genes related to housekeeping
functions and immune, sensory perception and response
to stimulus respectively.
Authors’ contributions
Khobondo J.O. conceived and designed the experiments,
developed perl script, wrote the manuscript; Kahi A.K.
discussed and improved manuscript; Ngeno K. analysed the
data, improved the manuscript. All authors read and approved
the final manuscript.
References
Basak S., and Ghosh T.C., 2005, On the origin of genomic adaptation at
high temperature for prokaryotic organisms, Biochemical and
Biophysical Research Communications, 330: 629-632
Freeman J.L., Perry G.H., Feuk L., Redon R., McCarroll S.A., Altshuler
D.M., Aburatani H., Jones K.W., Tyler-Smith C., Hurles M.E., Carter
N.P., Scherer S.W., and Lee C., 2006, Copy number variation: new
insights in genome diversity, Genome Res, 16: 949-961
Groenen M.A., Archibald A.L., Uenishi H., Tuggle C.K., Takeuchi Y., Rothschild
M.F., and Fairley S., 2012, Analyses of pig genomes provide insight into
porcine demography and evolution, Nature, 491(7424): 393-398
Griffith T.S., Brunner T., Fletcher S.M., Green D.R., and Ferguson T.A.,
1995, Fas ligand-induced apoptosis as a mechanism of immune
privilege, Science, 270(5239): 1189-1192
Hahn M.W., and Kern A.D., 2005, Comparative Genomics of Centrality and
Essentiality in Three Eukaryotic Protein-Interaction Networks,
Molecular Biology and Evolution, 22: 803-806
Hershberg R., and Petrov D.A., 2008, Selection on Codon Bias, Annual
Review of Genetics, 42: 287-299
Hershberg R., and Petrov D.A., 2010, Evidence That Mutation Is
Universally Biased towards AT in Bacteria, PLoS Genetic, 6: e1001115
Jia R., Cheng A., Wang M., Xin H., Guo Y., Zhu D., Qi X., Zhao L., Ge H.,
and Chen X., 2009, Analysis of synonymous codon usage in the UL24
gene of duck enteritis virus, Virus Genes, 38: 96-103
Kanaya S., Yamada Y., Kinouchi M., Kudo Y., and Ikemura T., 2001, Codon
Usage and tRNA Genes in Eukaryotes: Correlation of Codon Usage
Diversity with Translation Efficiency and with CG-Dinucleotide Usage
as Assessed by Multivariate Analysis, Journal of Molecular Evolution,
53: 290-298
Khobondo J.O., Okeno T.O., and Kahi A.K., 2015, Genomic composition
factors affect codon usage in porcine genome, African Journal of
Biotechnology, 14(4): 341-349
Kimura Y., and Tanaka K., 2010, Regulatory mechanisms involved in the
control of ubiquitin homeostasis, Journal of Biochemistry, 147: 793-798
Knight R., Freeland S., and Landweber L., 2001, A simple model based on
mutation and selection explains trends in codon and amino-acid usage
and GC composition within and across genomes, Genome Biology, 2:
research0010.1 - research0010.13
Maere S., Heymans K., Kuiper M., 2005, BiNGO: a Cytoscape plugin to
assess overrepresentation of gene ontology categories in biological
networks, Bioinformatics, 21:3448-3449
Nguyen D., Lee K., Choi H., Choi M., Le M., Song N., Kim J-H., Seo H.,
Oh J-W., Lee K., Kim T-H., Park C., 2012, The complete swine
olfactory subgenome: expansion of the olfactory gene repertoire in the
pig genome, BMC Genomics, 13: 584
Olave I., Wang W., Xue Y., Kuo A., and Crabtree G.R., 2002, Identification
of a polymorphic, neuron-specific chromatin remodeling complex,
Genes and Development, 16: 2509-2517
Paudel Y., Madsen O., Megens H.J., Frantz L.A., Bosse M., Bastiaansen
J.W., and Groenen M.A., 2013, Evolutionary dynamics of copy number
variation in pig genomes in the context of adaptation and domestication,
BMC genomics, 14(1): 449
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