Selection pressure on human STR loci and its relevance in repeat expansion disease

Makoto K. Shimada, Ryoko Sanbonmatsu, Yumi Yamaguchi-Kabata, Chisato Yamasaki, Yoshiyuki Suzuki, Ranajit Chakraborty, Takashi Gojobori, Tadashi Imanishi

研究成果: Article

6 引用 (Scopus)

抄録

Short Tandem Repeats (STRs) comprise repeats of one to several base pairs. Because of the high mutability due to strand slippage during DNA synthesis, rapid evolutionary change in the number of repeating units directly shapes the range of repeat-number variation according to selection pressure. However, the remaining questions include: Why are STRs causing repeat expansion diseases maintained in the human population; and why are these limited to neurodegenerative diseases? By evaluating the genome-wide selection pressure on STRs using the database we constructed, we identified two different patterns of relationship in repeat-number polymorphisms between DNA and amino-acid sequences, although both patterns are evolutionary consequences of avoiding the formation of harmful long STRs. First, a mixture of degenerate codons is represented in poly-proline (poly-P) repeats. Second, long poly-glutamine (poly-Q) repeats are favored at the protein level; however, at the DNA level, STRs encoding long poly-Qs are frequently divided by synonymous SNPs. Furthermore, significant enrichments of apoptosis and neurodevelopment were biological processes found specifically in genes encoding poly-Qs with repeat polymorphism. This suggests the existence of a specific molecular function for polymorphic and/or long poly-Q stretches. Given that the poly-Qs causing expansion diseases were longer than other poly-Qs, even in healthy subjects, our results indicate that the evolutionary benefits of long and/or polymorphic poly-Q stretches outweigh the risks of long CAG repeats predisposing to pathological hyper-expansions. Molecular pathways in neurodevelopment requiring long and polymorphic poly-Q stretches may provide a clue to understanding why poly-Q expansion diseases are limited to neurodegenerative diseases.

元の言語English
ページ(範囲)1851-1869
ページ数19
ジャーナルMolecular Genetics and Genomics
291
発行部数5
DOI
出版物ステータスPublished - 01-10-2016

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Microsatellite Repeats
Pressure
Neurodegenerative Diseases
DNA
Biological Phenomena
Proline
Codon
Base Pairing
Single Nucleotide Polymorphism
Amino Acid Sequence
Healthy Volunteers
Genome
Databases
Apoptosis
Population
Genes
Proteins

All Science Journal Classification (ASJC) codes

  • Molecular Biology
  • Genetics

これを引用

Shimada, M. K., Sanbonmatsu, R., Yamaguchi-Kabata, Y., Yamasaki, C., Suzuki, Y., Chakraborty, R., ... Imanishi, T. (2016). Selection pressure on human STR loci and its relevance in repeat expansion disease. Molecular Genetics and Genomics, 291(5), 1851-1869. https://doi.org/10.1007/s00438-016-1219-7
Shimada, Makoto K. ; Sanbonmatsu, Ryoko ; Yamaguchi-Kabata, Yumi ; Yamasaki, Chisato ; Suzuki, Yoshiyuki ; Chakraborty, Ranajit ; Gojobori, Takashi ; Imanishi, Tadashi. / Selection pressure on human STR loci and its relevance in repeat expansion disease. :: Molecular Genetics and Genomics. 2016 ; 巻 291, 番号 5. pp. 1851-1869.
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Shimada, MK, Sanbonmatsu, R, Yamaguchi-Kabata, Y, Yamasaki, C, Suzuki, Y, Chakraborty, R, Gojobori, T & Imanishi, T 2016, 'Selection pressure on human STR loci and its relevance in repeat expansion disease', Molecular Genetics and Genomics, 巻. 291, 番号 5, pp. 1851-1869. https://doi.org/10.1007/s00438-016-1219-7

Selection pressure on human STR loci and its relevance in repeat expansion disease. / Shimada, Makoto K.; Sanbonmatsu, Ryoko; Yamaguchi-Kabata, Yumi; Yamasaki, Chisato; Suzuki, Yoshiyuki; Chakraborty, Ranajit; Gojobori, Takashi; Imanishi, Tadashi.

:: Molecular Genetics and Genomics, 巻 291, 番号 5, 01.10.2016, p. 1851-1869.

研究成果: Article

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AU - Sanbonmatsu, Ryoko

AU - Yamaguchi-Kabata, Yumi

AU - Yamasaki, Chisato

AU - Suzuki, Yoshiyuki

AU - Chakraborty, Ranajit

AU - Gojobori, Takashi

AU - Imanishi, Tadashi

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Shimada MK, Sanbonmatsu R, Yamaguchi-Kabata Y, Yamasaki C, Suzuki Y, Chakraborty R その他. Selection pressure on human STR loci and its relevance in repeat expansion disease. Molecular Genetics and Genomics. 2016 10 1;291(5):1851-1869. https://doi.org/10.1007/s00438-016-1219-7