TY - JOUR
T1 - Substitution rate and structural divergence of 5′UTR evolution
T2 - Comparative analysis between human and cynomolgus monkey cDNAs
AU - Osada, Naoki
AU - Hirata, Makoto
AU - Tanuma, Reiko
AU - Kusuda, Jun
AU - Hida, Munetomo
AU - Suzuki, Yutaka
AU - Sugano, Sumio
AU - Gojobori, Takashi
AU - Shen, C. K.James
AU - Wu, Chung I.
AU - Hashimoto, Katsuyuki
PY - 2005/10
Y1 - 2005/10
N2 - The substitution rate and structural divergence in the 5′- untranslated region (UTR) were investigated by using human and cynomolgus monkey cDNA sequences. Due to the weaker functional constraint in the UTR than in the coding sequence, the divergence between humans and macaques would provide a good estimate of the nucleotide substitution rate and structural divergence in the 5′UTR. We found that the substitution rate in the 5′UTR (K 5UTR) averaged ≈10%-20% lower than the synonymous substitution rate (K s). However, both the K 5UTR and nonsynonymous substitution rate (K a) were significantly higher in the testicular cDNAs than in the brain cDNAs, whereas the K s did not differ. Further, an in silico analysis revealed that 27% (169/622) of macaque testicular cDNAs had an altered exon-intron structure in the 5′UTR compared with the human cDNAs. The fraction of cDNAs with an exon alteration was significantly higher in the testicular cDNAs than in the brain cDNAs. We confirmed by using reverse transcriptase-polymerase chain reaction that about one-third (6/16) of in silico "macaque-specific" exons in the 5′UTR were actually macaque specific in the testis. The results imply that positive selection increased K 5UTR and structural alteration rate of a certain fraction of genes as well as K a. We found that both positive and negative selection can act on the 5′UTR sequences.
AB - The substitution rate and structural divergence in the 5′- untranslated region (UTR) were investigated by using human and cynomolgus monkey cDNA sequences. Due to the weaker functional constraint in the UTR than in the coding sequence, the divergence between humans and macaques would provide a good estimate of the nucleotide substitution rate and structural divergence in the 5′UTR. We found that the substitution rate in the 5′UTR (K 5UTR) averaged ≈10%-20% lower than the synonymous substitution rate (K s). However, both the K 5UTR and nonsynonymous substitution rate (K a) were significantly higher in the testicular cDNAs than in the brain cDNAs, whereas the K s did not differ. Further, an in silico analysis revealed that 27% (169/622) of macaque testicular cDNAs had an altered exon-intron structure in the 5′UTR compared with the human cDNAs. The fraction of cDNAs with an exon alteration was significantly higher in the testicular cDNAs than in the brain cDNAs. We confirmed by using reverse transcriptase-polymerase chain reaction that about one-third (6/16) of in silico "macaque-specific" exons in the 5′UTR were actually macaque specific in the testis. The results imply that positive selection increased K 5UTR and structural alteration rate of a certain fraction of genes as well as K a. We found that both positive and negative selection can act on the 5′UTR sequences.
KW - 5′UTR
KW - Alternative splicing
KW - Evolution
KW - Primates
KW - Substitution rate
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U2 - 10.1093/molbev/msi187
DO - 10.1093/molbev/msi187
M3 - Article
C2 - 15944441
AN - SCOPUS:24744455048
SN - 0737-4038
VL - 22
SP - 1976
EP - 1982
JO - Molecular Biology and Evolution
JF - Molecular Biology and Evolution
IS - 10
ER -