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Commit 632c4be4 authored by Sebastian Triesch's avatar Sebastian Triesch
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Update README.md

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......@@ -21,5 +21,27 @@ This project was mainly conducted at the [Institute of Plant Biochemistry at HHU
- https://orcid.org/0000-0002-9134-6511
- Benjamin Stich
- https://orcid.org/0000-0001-6791-8068
- Steven Kelly
- https://orcid.org/0000-0003-1250-7055
- Andreas P.M.Weber
- https://orcid.org/0000-0003-0970-4672
## Abstract
C3-C4 intermediate photosynthesis has evolved at least five times convergently in the Brassicaceae, despite
this family lacking _bona fide_ C4 species. The establishment of this carbon concentrating mechanism is known
to require a complex suite of ultrastructural modifications as well as changes in spatial expression patterns,
which are both thought to be underpinned by a reconfiguration of existing gene-regulatory networks. However,
to date, the mechanisms which underpin the reconfiguration of these gene networks are largely unknown.
In this study, we used a pan-genomic association approach to identify genomic features that could confer
differential gene expression toward the C3-C4 intermediate state by analysing eight C3 species and seven
C3-C4 species from five independent origins in the Brassicaceae. We found a strong correlation between
transposable element (TE) insertions in cis-regulatory regions and the C3-C4 intermediacy. Specifically, our
study revealed 113 gene models in which presence of a TE within a gene correlates with C3-C4 intermediate
photosynthesis. In this set, genes involved in the photorespiratory glycine shuttle are enriched, including the
glycine decarboxylase P-protein whose expression domain undergoes a spatial shift during the transition to
C3-C4 photosynthesis. When further interrogating this gene, we discovered independent TE insertions in its
upstream region which we conclude to be responsible for causing the spatial shift in _GLDP1_ gene expression.
Our findings hint at a pivotal role of TEs in the evolution of C3-C4 intermediacy, especially in mediating
differential spatial gene expression.
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