Full-length RNA structure prediction of the HIV-1 genome reveals a conserved core domain

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Standard

Full-length RNA structure prediction of the HIV-1 genome reveals a conserved core domain. / Sükösd, Zsuzsanna; Andersen, Ebbe Sloth; Seemann, Ernst Stefan; Jensen, Mads Krogh; Hansen, Mathias; Gorodkin, Jan; Kjems, Jørgen.

In: Nucleic Acids Research, Vol. 43, No. 21, 02.12.2015, p. 10168-79.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Sükösd, Z, Andersen, ES, Seemann, ES, Jensen, MK, Hansen, M, Gorodkin, J & Kjems, J 2015, 'Full-length RNA structure prediction of the HIV-1 genome reveals a conserved core domain', Nucleic Acids Research, vol. 43, no. 21, pp. 10168-79. https://doi.org/10.1093/nar/gkv1039

APA

Sükösd, Z., Andersen, E. S., Seemann, E. S., Jensen, M. K., Hansen, M., Gorodkin, J., & Kjems, J. (2015). Full-length RNA structure prediction of the HIV-1 genome reveals a conserved core domain. Nucleic Acids Research, 43(21), 10168-79. https://doi.org/10.1093/nar/gkv1039

Vancouver

Sükösd Z, Andersen ES, Seemann ES, Jensen MK, Hansen M, Gorodkin J et al. Full-length RNA structure prediction of the HIV-1 genome reveals a conserved core domain. Nucleic Acids Research. 2015 Dec 2;43(21):10168-79. https://doi.org/10.1093/nar/gkv1039

Author

Sükösd, Zsuzsanna ; Andersen, Ebbe Sloth ; Seemann, Ernst Stefan ; Jensen, Mads Krogh ; Hansen, Mathias ; Gorodkin, Jan ; Kjems, Jørgen. / Full-length RNA structure prediction of the HIV-1 genome reveals a conserved core domain. In: Nucleic Acids Research. 2015 ; Vol. 43, No. 21. pp. 10168-79.

Bibtex

@article{01be223a6b0341ada7b5f08039f0662f,
title = "Full-length RNA structure prediction of the HIV-1 genome reveals a conserved core domain",
abstract = "A distance constrained secondary structural model of the ≈10 kb RNA genome of the HIV-1 has been predicted but higher-order structures, involving long distance interactions, are currently unknown. We present the first global RNA secondary structure model for the HIV-1 genome, which integrates both comparative structure analysis and information from experimental data in a full-length prediction without distance constraints. Besides recovering known structural elements, we predict several novel structural elements that are conserved in HIV-1 evolution. Our results also indicate that the structure of the HIV-1 genome is highly variable in most regions, with a limited number of stable and conserved RNA secondary structures. Most interesting, a set of long distance interactions form a core organizing structure (COS) that organize the genome into three major structural domains. Despite overlapping protein-coding regions the COS is supported by a particular high frequency of compensatory base changes, suggesting functional importance for this element. This new structural element potentially organizes the whole genome into three major domains protruding from a conserved core structure with potential roles in replication and evolution for the virus.",
author = "Zsuzsanna S{\"u}k{\"o}sd and Andersen, {Ebbe Sloth} and Seemann, {Ernst Stefan} and Jensen, {Mads Krogh} and Mathias Hansen and Jan Gorodkin and J{\o}rgen Kjems",
note = "{\textcopyright} The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research.",
year = "2015",
month = dec,
day = "2",
doi = "10.1093/nar/gkv1039",
language = "English",
volume = "43",
pages = "10168--79",
journal = "Nucleic Acids Research",
issn = "0305-1048",
publisher = "Oxford University Press",
number = "21",

}

RIS

TY - JOUR

T1 - Full-length RNA structure prediction of the HIV-1 genome reveals a conserved core domain

AU - Sükösd, Zsuzsanna

AU - Andersen, Ebbe Sloth

AU - Seemann, Ernst Stefan

AU - Jensen, Mads Krogh

AU - Hansen, Mathias

AU - Gorodkin, Jan

AU - Kjems, Jørgen

N1 - © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research.

PY - 2015/12/2

Y1 - 2015/12/2

N2 - A distance constrained secondary structural model of the ≈10 kb RNA genome of the HIV-1 has been predicted but higher-order structures, involving long distance interactions, are currently unknown. We present the first global RNA secondary structure model for the HIV-1 genome, which integrates both comparative structure analysis and information from experimental data in a full-length prediction without distance constraints. Besides recovering known structural elements, we predict several novel structural elements that are conserved in HIV-1 evolution. Our results also indicate that the structure of the HIV-1 genome is highly variable in most regions, with a limited number of stable and conserved RNA secondary structures. Most interesting, a set of long distance interactions form a core organizing structure (COS) that organize the genome into three major structural domains. Despite overlapping protein-coding regions the COS is supported by a particular high frequency of compensatory base changes, suggesting functional importance for this element. This new structural element potentially organizes the whole genome into three major domains protruding from a conserved core structure with potential roles in replication and evolution for the virus.

AB - A distance constrained secondary structural model of the ≈10 kb RNA genome of the HIV-1 has been predicted but higher-order structures, involving long distance interactions, are currently unknown. We present the first global RNA secondary structure model for the HIV-1 genome, which integrates both comparative structure analysis and information from experimental data in a full-length prediction without distance constraints. Besides recovering known structural elements, we predict several novel structural elements that are conserved in HIV-1 evolution. Our results also indicate that the structure of the HIV-1 genome is highly variable in most regions, with a limited number of stable and conserved RNA secondary structures. Most interesting, a set of long distance interactions form a core organizing structure (COS) that organize the genome into three major structural domains. Despite overlapping protein-coding regions the COS is supported by a particular high frequency of compensatory base changes, suggesting functional importance for this element. This new structural element potentially organizes the whole genome into three major domains protruding from a conserved core structure with potential roles in replication and evolution for the virus.

U2 - 10.1093/nar/gkv1039

DO - 10.1093/nar/gkv1039

M3 - Journal article

C2 - 26476446

VL - 43

SP - 10168

EP - 10179

JO - Nucleic Acids Research

JF - Nucleic Acids Research

SN - 0305-1048

IS - 21

ER -

ID: 160606030