Control of ribosome traffic by position-dependent choice of synonymous codons

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Control of ribosome traffic by position-dependent choice of synonymous codons. / Mitarai, Namiko; Pedersen, Steen.

I: Physical Biology, Bind 10, Nr. 5, 056011, 08.10.2013.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Mitarai, N & Pedersen, S 2013, 'Control of ribosome traffic by position-dependent choice of synonymous codons', Physical Biology, bind 10, nr. 5, 056011. https://doi.org/10.1088/1478-3975/10/5/056011

APA

Mitarai, N., & Pedersen, S. (2013). Control of ribosome traffic by position-dependent choice of synonymous codons. Physical Biology, 10(5), [056011]. https://doi.org/10.1088/1478-3975/10/5/056011

Vancouver

Mitarai N, Pedersen S. Control of ribosome traffic by position-dependent choice of synonymous codons. Physical Biology. 2013 okt. 8;10(5). 056011. https://doi.org/10.1088/1478-3975/10/5/056011

Author

Mitarai, Namiko ; Pedersen, Steen. / Control of ribosome traffic by position-dependent choice of synonymous codons. I: Physical Biology. 2013 ; Bind 10, Nr. 5.

Bibtex

@article{f9de526233a4480db9c03e7e5cadcbac,
title = "Control of ribosome traffic by position-dependent choice of synonymous codons",
abstract = "Messenger RNA (mRNA) encodes a sequence of amino acids by using codons. For most amino acids, there are multiple synonymous codons that can encode the amino acid. The translation speed can vary from one codon to another, thus there is room for changing the ribosome speed while keeping the amino acid sequence and hence the resulting protein. Recently, it has been noticed that the choice of the synonymous codon, via the resulting distribution of slow- and fast-translated codons, affects not only on the average speed of one ribosome translating the mRNA but also might have an effect on nearby ribosomes by affecting the appearance of 'traffic jams' where multiple ribosomes collide and form queues. To test this 'context effect' further, we here investigate the effect of the sequence of synonymous codons on the ribosome traffic by using a ribosome traffic model with codon-dependent rates, estimated from experiments. We compare the ribosome traffic on wild-type (WT) sequences and sequences where the synonymous codons were swapped randomly. By simulating translation of 87 genes, we demonstrate that the WT sequences, especially those with a high bias in codon usage, tend to have the ability to reduce ribosome collisions, hence optimizing the cellular investment in the translation apparatus. The magnitude of such reduction of the translation time might have a significant impact on the cellular growth rate and thereby have importance for the survival of the species.",
author = "Namiko Mitarai and Steen Pedersen",
year = "2013",
month = oct,
day = "8",
doi = "10.1088/1478-3975/10/5/056011",
language = "English",
volume = "10",
journal = "Physical Biology",
issn = "1478-3967",
publisher = "Institute of Physics Publishing Ltd",
number = "5",

}

RIS

TY - JOUR

T1 - Control of ribosome traffic by position-dependent choice of synonymous codons

AU - Mitarai, Namiko

AU - Pedersen, Steen

PY - 2013/10/8

Y1 - 2013/10/8

N2 - Messenger RNA (mRNA) encodes a sequence of amino acids by using codons. For most amino acids, there are multiple synonymous codons that can encode the amino acid. The translation speed can vary from one codon to another, thus there is room for changing the ribosome speed while keeping the amino acid sequence and hence the resulting protein. Recently, it has been noticed that the choice of the synonymous codon, via the resulting distribution of slow- and fast-translated codons, affects not only on the average speed of one ribosome translating the mRNA but also might have an effect on nearby ribosomes by affecting the appearance of 'traffic jams' where multiple ribosomes collide and form queues. To test this 'context effect' further, we here investigate the effect of the sequence of synonymous codons on the ribosome traffic by using a ribosome traffic model with codon-dependent rates, estimated from experiments. We compare the ribosome traffic on wild-type (WT) sequences and sequences where the synonymous codons were swapped randomly. By simulating translation of 87 genes, we demonstrate that the WT sequences, especially those with a high bias in codon usage, tend to have the ability to reduce ribosome collisions, hence optimizing the cellular investment in the translation apparatus. The magnitude of such reduction of the translation time might have a significant impact on the cellular growth rate and thereby have importance for the survival of the species.

AB - Messenger RNA (mRNA) encodes a sequence of amino acids by using codons. For most amino acids, there are multiple synonymous codons that can encode the amino acid. The translation speed can vary from one codon to another, thus there is room for changing the ribosome speed while keeping the amino acid sequence and hence the resulting protein. Recently, it has been noticed that the choice of the synonymous codon, via the resulting distribution of slow- and fast-translated codons, affects not only on the average speed of one ribosome translating the mRNA but also might have an effect on nearby ribosomes by affecting the appearance of 'traffic jams' where multiple ribosomes collide and form queues. To test this 'context effect' further, we here investigate the effect of the sequence of synonymous codons on the ribosome traffic by using a ribosome traffic model with codon-dependent rates, estimated from experiments. We compare the ribosome traffic on wild-type (WT) sequences and sequences where the synonymous codons were swapped randomly. By simulating translation of 87 genes, we demonstrate that the WT sequences, especially those with a high bias in codon usage, tend to have the ability to reduce ribosome collisions, hence optimizing the cellular investment in the translation apparatus. The magnitude of such reduction of the translation time might have a significant impact on the cellular growth rate and thereby have importance for the survival of the species.

U2 - 10.1088/1478-3975/10/5/056011

DO - 10.1088/1478-3975/10/5/056011

M3 - Journal article

C2 - 24104350

VL - 10

JO - Physical Biology

JF - Physical Biology

SN - 1478-3967

IS - 5

M1 - 056011

ER -

ID: 90623768