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Plant Genome Evolution, Amsterdam, The Netherlands, September 6th-8th 2015 alj@uin.no
Basin-wide transcriptomic response of the eelgrass Zostera marina
to a simulated heatwave
Jueterbock A.1,∗
, Franssen S.U.2
, Bergmann N.3
, Gu, J.4
, Coyer J.A.5
, Reusch T.B.H. 6
, Bornberg-Bauer E.4
, Olsen J.L.7
1 Faculty of Biosciences and Aquaculture, University of Nordland, BodĂž, Norway
2 Institut fšur Populationsgenetik, Vetmeduni Vienna, Austria
3 Integrated School of Ocean Sciences (ISOS), Kiel University, Germany
4 Institute for Evolution and Biodiversity, University of Mšunster, Germany
5 Shoals Marine Laboratory, Cornell University, Portsmouth, USA
6 GEOMAR Helmholtz-Centre for Ocean Research Kiel, Evolutionary Ecology of Marine Fishes, Germany
7 Marine Benthic Ecology and Evolution Group, Centre for Ecological and Evolutionary Studies, University of Groningen, The Netherlands
13c3b7f
BACKGROUND
Heat waves are a major threat for Zostera marina, the pre-
dominant seagrass in the northern hemisphere. In previous
studies, Z. marina was found to be more heat tolerant at the
southern edge of its European distribution (Mediterranean, [1]).
Here, we asked whether inherent heat resistance is a unique
characteristic of Mediterranean seagrass or if Z. marina
adapted to warm temperatures in parallel along the Ameri-
can and European thermal clines.
METHODS
Sampling sites Common-garden heat-stress Bioinformatics data analysis
Weekly average sea surface temperature (SST) at four sam-
pling sites with contrasting thermal regimes.
Following 50 days of acclimation, we created a realistic heat-
wave and recovery period.
Samples for RNAseq were taken at two time points under heat-
stress (T2 and T3: 0 and 5 days at 25.5◩
C) and at three time
points under recovery (T5. T7. and T9: 1, 20, and 30 days at
19◩
C) along with control samples at all ïŹve time points.
WorkïŹ‚ow of data analysis with color codes representing
grouping of samples/libraries.
Location G (Gabicce Mare) D (Doverodde) W (Waquoit) GB (Great Bay)
Atlantic/Mediterranean M A
North/South S N S N
Condition Control Heated Recovery C H R C H R C H R
Timepoint 2 3 5 7 9 2 3 5 7 9
Genotype, Library 1 2 3
RNAseq (Illumina) + Quality control
Alignment (splice-aware)
Zostera marina genome
Annotation
Filtering reads
Duplicates
Ambiguous mappings
Non-annotated mappings
Expression proïŹles (rlog transformed)
Gene Library 1 Library 2 Library 3 ...
mRNA1 3.6 5.9 6.4 ...
... ... ... ... ...
RESULTS AND DISCUSSION
Heat response Adaptive differentiation Frontloaded genes
Heat-responsive genes (ca. 3300) were more differently ex-
pressed between Mediterranean and Atlantic samples than
between Northern and Southern samples, both under heat-
stress and under control/recovery conditions.
Hierarchical cluster on the ïŹrst ïŹve principal components of
heat-responsive gene expression in all samples.
D: Doverodde, G: Gabicce Mare, GB: Great Bay, W: Waquoit;
c: control samples, w: stressed samples. Numbers indicate
sampling time points.
At 21 genes, Mediterranean samples showed expression differ-
ences from Atlantic samples that were putatively adaptive to
contrasting temperatures, as these genes were also adap-
tively differentiated between Northern and Southern samples.
Venn diagram of adaptively differentiated genes.
Differentially expressed (gray numbers) or adaptively differenti-
ated (black numbers) genes between Atlantic (A) and Mediter-
ranean (M) samples and between Northern (N) and Southern
(S) samples.
In 498 genes the Mediterranean samples showed higher con-
stitutive expression than the Atlantic samples.
Enriched molecular functions in the frontloaded frontloaded
genes were dominated by’methyltransferase activity’ (epigenetic
regulation of gene expression).
The size of the rectangles reïŹ‚ect the p-value for enrichment.
Faster recovery of gene expression in both southern popula-
tions suggests reduced sensitivity to global warming at the
species’ southern edge of distribution.
Much of the previously observed North-South differentiation
along the European coast [e.g. 1] might be explained by the
adaptive transcriptomic differentiation between Mediter-
ranean and Atlantic seagrass.
Frontloading of heat-responsive genes may convey heat-
hardening in Mediterranean seagrass. Differential methyla-
tion could explain the rapid transcriptomic differentiation of
Mediterranean from Atlantic seagrass.
References
[1] Franssen SU, Gu J, Bergmann N, Winters G, Klostermeier UC, Rosenstiel P, Bornberg-Bauer E & Reusch, TBH (2011): Transcriptomic resilience
to global warming in the seagrass Zostera marina, a marine foundation species. Proceedings of the National Academy of Sciences
108(48):19276–19281
CONCLUSIONS
Faster recovery and parallel transcriptomic differentiation of
the two Southern seagrass populations suggest that Z. marina
adapted to warm temperatures at least partly (at 24 genes) in
parallel along the European and Atlantic thermal clines. Most
of the transcriptomic North-South differentiation along the Euro-
pean coast, however, can be explained by strong adaptive dif-
ferentiation (at 170 genes) between Atlantic and Mediter-
ranean seagrass. Transcriptomic adaptation to the thermally
unique Mediterranean must have been rapid and might have
been driven by epigenetic regulation of gene expression.
Constitutive overexpression of heat responsive genes might be
energetically costly and, instead of reducing sensitivity to cli-
mate change, could undermine the potential of Mediterranean
seagrass to respond to additional anthropogenic stress.

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Basin-wide transcriptomic response of the eelgrass Zostera marina to a simulated heatwave

  • 1. Plant Genome Evolution, Amsterdam, The Netherlands, September 6th-8th 2015 alj@uin.no Basin-wide transcriptomic response of the eelgrass Zostera marina to a simulated heatwave Jueterbock A.1,∗ , Franssen S.U.2 , Bergmann N.3 , Gu, J.4 , Coyer J.A.5 , Reusch T.B.H. 6 , Bornberg-Bauer E.4 , Olsen J.L.7 1 Faculty of Biosciences and Aquaculture, University of Nordland, BodĂž, Norway 2 Institut fšur Populationsgenetik, Vetmeduni Vienna, Austria 3 Integrated School of Ocean Sciences (ISOS), Kiel University, Germany 4 Institute for Evolution and Biodiversity, University of Mšunster, Germany 5 Shoals Marine Laboratory, Cornell University, Portsmouth, USA 6 GEOMAR Helmholtz-Centre for Ocean Research Kiel, Evolutionary Ecology of Marine Fishes, Germany 7 Marine Benthic Ecology and Evolution Group, Centre for Ecological and Evolutionary Studies, University of Groningen, The Netherlands 13c3b7f BACKGROUND Heat waves are a major threat for Zostera marina, the pre- dominant seagrass in the northern hemisphere. In previous studies, Z. marina was found to be more heat tolerant at the southern edge of its European distribution (Mediterranean, [1]). Here, we asked whether inherent heat resistance is a unique characteristic of Mediterranean seagrass or if Z. marina adapted to warm temperatures in parallel along the Ameri- can and European thermal clines. METHODS Sampling sites Common-garden heat-stress Bioinformatics data analysis Weekly average sea surface temperature (SST) at four sam- pling sites with contrasting thermal regimes. Following 50 days of acclimation, we created a realistic heat- wave and recovery period. Samples for RNAseq were taken at two time points under heat- stress (T2 and T3: 0 and 5 days at 25.5◩ C) and at three time points under recovery (T5. T7. and T9: 1, 20, and 30 days at 19◩ C) along with control samples at all ïŹve time points. WorkïŹ‚ow of data analysis with color codes representing grouping of samples/libraries. Location G (Gabicce Mare) D (Doverodde) W (Waquoit) GB (Great Bay) Atlantic/Mediterranean M A North/South S N S N Condition Control Heated Recovery C H R C H R C H R Timepoint 2 3 5 7 9 2 3 5 7 9 Genotype, Library 1 2 3 RNAseq (Illumina) + Quality control Alignment (splice-aware) Zostera marina genome Annotation Filtering reads Duplicates Ambiguous mappings Non-annotated mappings Expression proïŹles (rlog transformed) Gene Library 1 Library 2 Library 3 ... mRNA1 3.6 5.9 6.4 ... ... ... ... ... ... RESULTS AND DISCUSSION Heat response Adaptive differentiation Frontloaded genes Heat-responsive genes (ca. 3300) were more differently ex- pressed between Mediterranean and Atlantic samples than between Northern and Southern samples, both under heat- stress and under control/recovery conditions. Hierarchical cluster on the ïŹrst ïŹve principal components of heat-responsive gene expression in all samples. D: Doverodde, G: Gabicce Mare, GB: Great Bay, W: Waquoit; c: control samples, w: stressed samples. Numbers indicate sampling time points. At 21 genes, Mediterranean samples showed expression differ- ences from Atlantic samples that were putatively adaptive to contrasting temperatures, as these genes were also adap- tively differentiated between Northern and Southern samples. Venn diagram of adaptively differentiated genes. Differentially expressed (gray numbers) or adaptively differenti- ated (black numbers) genes between Atlantic (A) and Mediter- ranean (M) samples and between Northern (N) and Southern (S) samples. In 498 genes the Mediterranean samples showed higher con- stitutive expression than the Atlantic samples. Enriched molecular functions in the frontloaded frontloaded genes were dominated by’methyltransferase activity’ (epigenetic regulation of gene expression). The size of the rectangles reïŹ‚ect the p-value for enrichment. Faster recovery of gene expression in both southern popula- tions suggests reduced sensitivity to global warming at the species’ southern edge of distribution. Much of the previously observed North-South differentiation along the European coast [e.g. 1] might be explained by the adaptive transcriptomic differentiation between Mediter- ranean and Atlantic seagrass. Frontloading of heat-responsive genes may convey heat- hardening in Mediterranean seagrass. Differential methyla- tion could explain the rapid transcriptomic differentiation of Mediterranean from Atlantic seagrass. References [1] Franssen SU, Gu J, Bergmann N, Winters G, Klostermeier UC, Rosenstiel P, Bornberg-Bauer E & Reusch, TBH (2011): Transcriptomic resilience to global warming in the seagrass Zostera marina, a marine foundation species. Proceedings of the National Academy of Sciences 108(48):19276–19281 CONCLUSIONS Faster recovery and parallel transcriptomic differentiation of the two Southern seagrass populations suggest that Z. marina adapted to warm temperatures at least partly (at 24 genes) in parallel along the European and Atlantic thermal clines. Most of the transcriptomic North-South differentiation along the Euro- pean coast, however, can be explained by strong adaptive dif- ferentiation (at 170 genes) between Atlantic and Mediter- ranean seagrass. Transcriptomic adaptation to the thermally unique Mediterranean must have been rapid and might have been driven by epigenetic regulation of gene expression. Constitutive overexpression of heat responsive genes might be energetically costly and, instead of reducing sensitivity to cli- mate change, could undermine the potential of Mediterranean seagrass to respond to additional anthropogenic stress.