umu.sePublications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
The gut microbiome participates in transgenerational inheritance of low temperature responses in Drosophila melanogaster
Umeå University, Faculty of Science and Technology, Department of Molecular Biology (Faculty of Science and Technology). (Per Stenberg)ORCID iD: 0000-0003-1642-0301
Umeå University, Faculty of Science and Technology, Department of Molecular Biology (Faculty of Science and Technology). (Per Stenberg)
Umeå University, Faculty of Science and Technology, Department of Molecular Biology (Faculty of Science and Technology). Division of CBRN Security and Defence, FOI-Swedish, Defence Research Agency, Umeå, Sweden. (Per Stenberg)
Show others and affiliations
2018 (English)In: FEBS Letters, ISSN 0014-5793, E-ISSN 1873-3468, Vol. 592, no 24, p. 4078-4086Article in journal (Refereed) Published
Abstract [en]

Environmental perturbations induce transcriptional changes, some of which may be inherited even in the absence of the initial stimulus. Previous studies have focused on transfers through the germ-line although microbiota is also passed on to the offspring. Thus, we inspected the involvement of the gut microbiome in transgenerational inheritance of environmental exposures in Drosophila melanogaster. We grew flies in the cold versus control temperatures and compared their transcriptional patterns in both conditions as well as in their offspring. F2 flies grew in control temperature while we controlled their microbiota acquisition from either F1 sets. Transcriptional status of some genes was conserved transgenerationally, and a subset of these genes, mainly expressed in the gut, was transcriptionally dependent on the acquired microbiome. This article is protected by copyright. All rights reserved.

Place, publisher, year, edition, pages
John Wiley & Sons, 2018. Vol. 592, no 24, p. 4078-4086
National Category
Genetics
Identifiers
URN: urn:nbn:se:umu:diva-153266DOI: 10.1002/1873-3468.13278ISI: 000453789400008PubMedID: 30372516OAI: oai:DiVA.org:umu-153266DiVA, id: diva2:1262934
Funder
Knut and Alice Wallenberg FoundationAvailable from: 2018-11-13 Created: 2018-11-13 Last updated: 2019-01-08Bibliographically approved
In thesis
1. Regulation of gene expression in fruit flies: how does it start, and will it be remembered?
Open this publication in new window or tab >>Regulation of gene expression in fruit flies: how does it start, and will it be remembered?
2018 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

One of the most distinctive features of eukaryotic chromosomes is the bundling of DNA together with functionally associated RNA and proteins in chromatin. This allows huge amounts of DNA to be packed inside the very tiny space of the nucleus, and alterations in the structure of chromatin enable access to the DNA for transcription (“reading” genes by production of RNA copies). Much of the current knowledge of chromatin structure and regulation comes from studies of Drosophila melanogaster. When the chromatin structure is open the transcription of a gene can start after recruitment of the necessary factors. The main enzyme for gene transcription is Polymerase II (Pol II). For successful gene transcription, Pol II must not only be recruited to the gene’s promoter, but also escape from a pausing state which occurs soon after transcription initiation. CBP/P300 is one of the co-activators involved in transcriptional activation. In the studies this thesis is based upon, my colleagues and I (hereafter we) discovered a new function for CBP in transcription activation. Using high throughput sequencing techniques, we found that CBP directly stimulates recruitment of Pol II to promoters, and facilitates its release from the paused state, enabling progression to the elongation stage of transcription.

For cells to remember their identity following division during development, the transcriptional state of genes must be transmitted. Intensively studied players involved in this memory are the Polycomb group (PcG) proteins, responsible for maintaining the repressed state of important developmental genes. The core members are Polycomb repressive complex 1 and 2 (PRC1 and PRC2), which are recruited in flies through poorly known mechanisms to target genes by so-called Polycomb response elements (PREs). Using Drosophila mutant cell lines, we showed that (in contrast to previous models) some PREs can recruit PRC1 even when PRC2 is absent. We also observed that at many PREs, PRC1 is needed for recruitment of PRC2 and concluded that targeting PRC complexes to PREs is a much more flexible and variable process than previously thought.

Some phenotypic effects of environmental changes can be transferred to subsequent generations. Previous efforts to identify the mechanisms involved have focused on material (mainly, but not only, DNA) transferred through germ cells. However, organisms’ microbiomes are also transferred to the next generation. Thus, to investigate possible contributions of microbiomes to such transfer, we used fruit flies as the microbiomes they inherit can be easily controlled. We altered some parents’ environmental conditions by lowering the temperature, then grew offspring that received microbiomes from cold-treated and control parents in control conditions and compared their transcriptional patterns. Our results suggest that most of the crosstalk between the microbiome and the fly happens in the gut, and that further investigation of this previously unsuspected mode of inheritance is warranted.

Place, publisher, year, edition, pages
Umeå: Umeå University, Department of Molecular Biology, 2018. p. 47
Keywords
Drosophila, epigenetics, transcription, gene regulation, transcription maintenance, CBP, polymerase pausing, Polycomb group proteins, transgenerational inheritance of transcriptional response, gut microbiome
National Category
Bioinformatics and Systems Biology Biochemistry and Molecular Biology
Research subject
Molecular Biology
Identifiers
urn:nbn:se:umu:diva-153271 (URN)978-91-7601-973-3 (ISBN)
Public defence
2018-12-07, Astrid Fagreus lecture hall (A103), Sjukhusområdet, byggnader 6A, Umeå, 13:00 (English)
Opponent
Supervisors
Available from: 2018-11-16 Created: 2018-11-14 Last updated: 2018-11-15Bibliographically approved

Open Access in DiVA

fulltext(523 kB)79 downloads
File information
File name FULLTEXT01.pdfFile size 523 kBChecksum SHA-512
39c85cfd844decf951b80f7769ff8ec0d6063ed22b1741d7def725d896d65e76b300713a0c3c852f1686c191d0c670b4b1de35f059cf91238e371479a5aa3574
Type fulltextMimetype application/pdf

Other links

Publisher's full textPubMed

Authority records BETA

Zare, AmanJohansson, Anna-MiaKarlsson, EdvinDelhomme, NicolasStenberg, Per

Search in DiVA

By author/editor
Zare, AmanJohansson, Anna-MiaKarlsson, EdvinDelhomme, NicolasStenberg, Per
By organisation
Department of Molecular Biology (Faculty of Science and Technology)Department of Ecology and Environmental Sciences
In the same journal
FEBS Letters
Genetics

Search outside of DiVA

GoogleGoogle Scholar
Total: 79 downloads
The number of downloads is the sum of all downloads of full texts. It may include eg previous versions that are now no longer available

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 443 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf