---
_id: '8262'
abstract:
- lang: eng
  text: "Background: The genus Burkholderia consists of species that occupy remarkably
    diverse ecological niches. Its best known members are important pathogens, B.
    mallei and B. pseudomallei, which cause glanders and melioidosis, respectively.
    Burkholderia genomes are unusual due to their multichromosomal organization, generally
    comprised of 2-3 chromosomes.\r\n\r\nResults: We performed integrated genomic
    analysis of 127 Burkholderia strains. The pan-genome is open with the saturation
    to be reached between 86,000 and 88,000 genes. The reconstructed rearrangements
    indicate a strong avoidance of intra-replichore inversions that is likely caused
    by selection against the transfer of large groups of genes between the leading
    and the lagging strands. Translocated genes also tend to retain their position
    in the leading or the lagging strand, and this selection is stronger for large
    syntenies. Integrated reconstruction of chromosome rearrangements in the context
    of strains phylogeny reveals parallel rearrangements that may indicate inversion-based
    phase variation and integration of new genomic islands. In particular, we detected
    parallel inversions in the second chromosomes of B. pseudomallei with breakpoints
    formed by genes encoding membrane components of multidrug resistance complex,
    that may be linked to a phase variation mechanism. Two genomic islands, spreading
    horizontally between chromosomes, were detected in the B. cepacia group.\r\n\r\nConclusions:
    This study demonstrates the power of integrated analysis of pan-genomes, chromosome
    rearrangements, and selection regimes. Non-random inversion patterns indicate
    selective pressure, inversions are particularly frequent in a recent pathogen
    B. mallei, and, together with periods of positive selection at other branches,
    may indicate adaptation to new niches. One such adaptation could be a possible
    phase variation mechanism in B. pseudomallei."
article_number: '965'
article_processing_charge: No
article_type: original
author:
- first_name: Olga
  full_name: Bochkareva, Olga
  id: C4558D3C-6102-11E9-A62E-F418E6697425
  last_name: Bochkareva
  orcid: 0000-0003-1006-6639
- first_name: Elena V.
  full_name: Moroz, Elena V.
  last_name: Moroz
- first_name: Iakov I.
  full_name: Davydov, Iakov I.
  last_name: Davydov
- first_name: Mikhail S.
  full_name: Gelfand, Mikhail S.
  last_name: Gelfand
citation:
  ama: Bochkareva O, Moroz EV, Davydov II, Gelfand MS. Genome rearrangements and selection
    in multi-chromosome bacteria Burkholderia spp. <i>BMC Genomics</i>. 2018;19. doi:<a
    href="https://doi.org/10.1186/s12864-018-5245-1">10.1186/s12864-018-5245-1</a>
  apa: Bochkareva, O., Moroz, E. V., Davydov, I. I., &#38; Gelfand, M. S. (2018).
    Genome rearrangements and selection in multi-chromosome bacteria Burkholderia
    spp. <i>BMC Genomics</i>. Springer Nature. <a href="https://doi.org/10.1186/s12864-018-5245-1">https://doi.org/10.1186/s12864-018-5245-1</a>
  chicago: Bochkareva, Olga, Elena V. Moroz, Iakov I. Davydov, and Mikhail S. Gelfand.
    “Genome Rearrangements and Selection in Multi-Chromosome Bacteria Burkholderia
    Spp.” <i>BMC Genomics</i>. Springer Nature, 2018. <a href="https://doi.org/10.1186/s12864-018-5245-1">https://doi.org/10.1186/s12864-018-5245-1</a>.
  ieee: O. Bochkareva, E. V. Moroz, I. I. Davydov, and M. S. Gelfand, “Genome rearrangements
    and selection in multi-chromosome bacteria Burkholderia spp.,” <i>BMC Genomics</i>,
    vol. 19. Springer Nature, 2018.
  ista: Bochkareva O, Moroz EV, Davydov II, Gelfand MS. 2018. Genome rearrangements
    and selection in multi-chromosome bacteria Burkholderia spp. BMC Genomics. 19,
    965.
  mla: Bochkareva, Olga, et al. “Genome Rearrangements and Selection in Multi-Chromosome
    Bacteria Burkholderia Spp.” <i>BMC Genomics</i>, vol. 19, 965, Springer Nature,
    2018, doi:<a href="https://doi.org/10.1186/s12864-018-5245-1">10.1186/s12864-018-5245-1</a>.
  short: O. Bochkareva, E.V. Moroz, I.I. Davydov, M.S. Gelfand, BMC Genomics 19 (2018).
date_created: 2020-08-15T11:02:08Z
date_published: 2018-12-27T00:00:00Z
date_updated: 2023-02-23T13:28:52Z
day: '27'
doi: 10.1186/s12864-018-5245-1
extern: '1'
intvolume: '        19'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1186/s12864-018-5245-1
month: '12'
oa: 1
oa_version: Published Version
publication: BMC Genomics
publication_identifier:
  issn:
  - 1471-2164
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
status: public
title: Genome rearrangements and selection in multi-chromosome bacteria Burkholderia
  spp.
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 19
year: '2018'
...
---
_id: '20'
abstract:
- lang: eng
  text: 'Background: Norepinephrine (NE) signaling has a key role in white adipose
    tissue (WAT) functions, including lipolysis, free fatty acid liberation and, under
    certain conditions, conversion of white into brite (brown-in-white) adipocytes.
    However, acute effects of NE stimulation have not been described at the transcriptional
    network level. Results: We used RNA-seq to uncover a broad transcriptional response.
    The inference of protein-protein and protein-DNA interaction networks allowed
    us to identify a set of immediate-early genes (IEGs) with high betweenness, validating
    our approach and suggesting a hierarchical control of transcriptional regulation.
    In addition, we identified a transcriptional regulatory network with IEGs as master
    regulators, including HSF1 and NFIL3 as novel NE-induced IEG candidates. Moreover,
    a functional enrichment analysis and gene clustering into functional modules suggest
    a crosstalk between metabolic, signaling, and immune responses. Conclusions: Altogether,
    our network biology approach explores for the first time the immediate-early systems
    level response of human adipocytes to acute sympathetic activation, thereby providing
    a first network basis of early cell fate programs and crosstalks between metabolic
    and transcriptional networks required for proper WAT function.'
acknowledgement: This work was funded by the German Centre for Diabetes Research (DZD)
  and the Austrian Science Fund (FWF, P25729-B19).
article_processing_charge: No
article_type: original
author:
- first_name: Juan
  full_name: Higareda Almaraz, Juan
  last_name: Higareda Almaraz
- first_name: Michael
  full_name: Karbiener, Michael
  last_name: Karbiener
- first_name: Maude
  full_name: Giroud, Maude
  last_name: Giroud
- first_name: Florian
  full_name: Pauler, Florian
  id: 48EA0138-F248-11E8-B48F-1D18A9856A87
  last_name: Pauler
  orcid: 0000-0002-7462-0048
- first_name: Teresa
  full_name: Gerhalter, Teresa
  last_name: Gerhalter
- first_name: Stephan
  full_name: Herzig, Stephan
  last_name: Herzig
- first_name: Marcel
  full_name: Scheideler, Marcel
  last_name: Scheideler
citation:
  ama: Higareda Almaraz J, Karbiener M, Giroud M, et al. Norepinephrine triggers an
    immediate-early regulatory network response in primary human white adipocytes.
    <i>BMC Genomics</i>. 2018;19(1). doi:<a href="https://doi.org/10.1186/s12864-018-5173-0">10.1186/s12864-018-5173-0</a>
  apa: Higareda Almaraz, J., Karbiener, M., Giroud, M., Pauler, F., Gerhalter, T.,
    Herzig, S., &#38; Scheideler, M. (2018). Norepinephrine triggers an immediate-early
    regulatory network response in primary human white adipocytes. <i>BMC Genomics</i>.
    BioMed Central. <a href="https://doi.org/10.1186/s12864-018-5173-0">https://doi.org/10.1186/s12864-018-5173-0</a>
  chicago: Higareda Almaraz, Juan, Michael Karbiener, Maude Giroud, Florian Pauler,
    Teresa Gerhalter, Stephan Herzig, and Marcel Scheideler. “Norepinephrine Triggers
    an Immediate-Early Regulatory Network Response in Primary Human White Adipocytes.”
    <i>BMC Genomics</i>. BioMed Central, 2018. <a href="https://doi.org/10.1186/s12864-018-5173-0">https://doi.org/10.1186/s12864-018-5173-0</a>.
  ieee: J. Higareda Almaraz <i>et al.</i>, “Norepinephrine triggers an immediate-early
    regulatory network response in primary human white adipocytes,” <i>BMC Genomics</i>,
    vol. 19, no. 1. BioMed Central, 2018.
  ista: Higareda Almaraz J, Karbiener M, Giroud M, Pauler F, Gerhalter T, Herzig S,
    Scheideler M. 2018. Norepinephrine triggers an immediate-early regulatory network
    response in primary human white adipocytes. BMC Genomics. 19(1).
  mla: Higareda Almaraz, Juan, et al. “Norepinephrine Triggers an Immediate-Early
    Regulatory Network Response in Primary Human White Adipocytes.” <i>BMC Genomics</i>,
    vol. 19, no. 1, BioMed Central, 2018, doi:<a href="https://doi.org/10.1186/s12864-018-5173-0">10.1186/s12864-018-5173-0</a>.
  short: J. Higareda Almaraz, M. Karbiener, M. Giroud, F. Pauler, T. Gerhalter, S.
    Herzig, M. Scheideler, BMC Genomics 19 (2018).
date_created: 2018-12-11T11:44:12Z
date_published: 2018-11-03T00:00:00Z
date_updated: 2023-09-13T09:10:47Z
day: '03'
ddc:
- '570'
department:
- _id: SiHi
doi: 10.1186/s12864-018-5173-0
external_id:
  isi:
  - '000450976700002'
file:
- access_level: open_access
  checksum: a56516e734dab589dc7f3e1915973b4d
  content_type: application/pdf
  creator: dernst
  date_created: 2018-12-17T14:52:57Z
  date_updated: 2020-07-14T12:45:23Z
  file_id: '5712'
  file_name: 2018_BMCGenomics_Higareda.pdf
  file_size: 4629784
  relation: main_file
file_date_updated: 2020-07-14T12:45:23Z
has_accepted_license: '1'
intvolume: '        19'
isi: 1
issue: '1'
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
publication: BMC Genomics
publication_identifier:
  issn:
  - 1471-2164
publication_status: published
publisher: BioMed Central
publist_id: '8035'
quality_controlled: '1'
related_material:
  record:
  - id: '9807'
    relation: research_data
    status: public
  - id: '9808'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: Norepinephrine triggers an immediate-early regulatory network response in primary
  human white adipocytes
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 19
year: '2018'
...
