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Transcript
Analysis of Molecular Evolution in Mitochondrial tRNA
Gene Sequences
Jun-Ichi Sagara
Kentaro Shimizu
[email protected]
[email protected]
Department of Biotechnology, The University of Tokyo
1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.
1
Introduction
When studying about molecular evolution, it is very important to make phylogenetic trees from
correlation of each sequence. We therefore developed a computational method [1] based on principal
component analysis (PCA) and multidimensional scaling analysis (MDS). Our method is based on
that used by the Casari et al. [2] to predict functional residues in ras-rab-rho super family. We have
extended it to the analysis of tRNA gene sequences and have used it to identify the groups of bases
specific to particular species by applying its basic procedure recursively. The advantages of our method
are as follows; (1) it allows comparison of the whole sequence; (2) Gene sequences are represented as
vectors in a generalized sequence space; (3) the bases of each sequence are projected individually onto
the same sequence space. Applying this method to the sequences of all the mitochondrial tRNA genes,
we expect to detect not only bases that are always conserved but also bases that are often conserved.
2
Results
et ).
We classified mitochondrial tRNA gene sequences by each 21 tRNA species (containing tRNAM
f
In all the graphs of each 21 tRNA species, sequences divided four groups. They are “vertebrates,”
“arthropoda,” “plants and single cells/fungi,” and “echinoderms and nematoda/trematoda.” The
“echinoderms and nematoda/trematoda” group located in the middle of the other groups. This
means that echinoderms, nematoda and trematoda are turning point among the other species. Then,
we detected many characteristic bases in all the mitochondrial tRNA gene sequences of various species.
Most of characteristic bases are in elbow region of tRNA (Fig. 2). The bases in the elbow region play
an influential role in determining the dynamics of the molecule [3]. Thus, the results suggest that
preserving the dynamics of the molecule of each tRNA is important to molecular evolution.
References
[1] Sagara, J.-I., Shimizu, S., Kawabata, T., Nakamura, S., Ikeguchi, M., and Shimizu, K., The use
of sequence comparison to detect ‘identities’ in tRNA genes, Nucleic Acids Res., 26:1974–1979,
1998.
[2] Casari, G., Sander, C., and Valencia, A., A method to predict functional residues in proteins,
Natl. Struc. Biol., 2:171–178, 1995.
[3] Nakamura, S. and Do, J., Dynamics of transfer RNAs analyzed by normal mode calculation,
Nucleic Acids Res., 22:514–521, 1994.
tRNA
Gln
single cell and fungi
plants
animals
insects
ascaris
c. elegance
echinina
fishes
amphibians reptoles
mammals
asterias
whales
birds
vertebrates
amoeba
chlamydomonadales
Figure 1: Plots of sequence of tRNAGln . Sequences are grouped by species related closely and separated
by species related distantly.
Figure 2: Characteristic bases (spacefill model) represented on the common 3-dimensional backbone
model of tRNA.