Umeå University's logo

umu.sePublications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • 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
Dissection of the Fgf8 regulatory landscape by in vivo CRISPR-editing reveals extensive intra- and inter-enhancer redundancy
Umeå University, Faculty of Medicine, Umeå Centre for Molecular Medicine (UCMM). Developmental Biology Unit, EMBL, Germany; (Epi)genomics of Animal Development Unit, Department of Developmental and Stem Cell Biology, Institut Pasteur, France; UMR3738, CNRS, Paris, France.ORCID iD: 0000-0003-1283-0784
Show others and affiliations
2021 (English)In: Nature Communications, E-ISSN 2041-1723, Vol. 12, no 1, article id 439Article in journal (Refereed) Published
Abstract [en]

Developmental genes are often regulated by multiple elements with overlapping activity. Yet, in most cases, the relative function of those elements and their contribution to endogenous gene expression remain poorly characterized. An example of this phenomenon is that distinct sets of enhancers have been proposed to direct Fgf8 in the limb apical ectodermal ridge and the midbrain-hindbrain boundary. Using in vivo CRISPR/Cas9 genome engineering, we functionally dissect this complex regulatory ensemble and demonstrate two distinct regulatory logics. In the apical ectodermal ridge, the control of Fgf8 expression appears distributed between different enhancers. In contrast, we find that in the midbrain-hindbrain boundary, one of the three active enhancers is essential while the other two are dispensable. We further dissect the essential midbrain-hindbrain boundary enhancer to reveal that it is also composed by a mixture of essential and dispensable modules. Cross-species transgenic analysis of this enhancer suggests that its composition may have changed in the vertebrate lineage.

Place, publisher, year, edition, pages
Springer Nature, 2021. Vol. 12, no 1, article id 439
National Category
Developmental Biology
Identifiers
URN: urn:nbn:se:umu:diva-180806DOI: 10.1038/s41467-020-20714-yISI: 000613518600007PubMedID: 33469032Scopus ID: 2-s2.0-85099540540OAI: oai:DiVA.org:umu-180806DiVA, id: diva2:1533115
Available from: 2021-03-03 Created: 2021-03-03 Last updated: 2023-03-28Bibliographically approved

Open Access in DiVA

fulltext(3508 kB)212 downloads
File information
File name FULLTEXT01.pdfFile size 3508 kBChecksum SHA-512
f9cb64405d7efa81dea0541d4f5b46e8b812b6bc9614171953e12f07f94f4ec7a5a1781a6ff9e853862ff6bf29f67ad512354656d0f45ef9af1d86117c9f1ef6
Type fulltextMimetype application/pdf

Other links

Publisher's full textPubMedScopus

Authority records

Hörnblad, Andreas

Search in DiVA

By author/editor
Hörnblad, Andreas
By organisation
Umeå Centre for Molecular Medicine (UCMM)
In the same journal
Nature Communications
Developmental Biology

Search outside of DiVA

GoogleGoogle Scholar
Total: 212 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: 722 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • 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