Publications
NIBIOs employees contribute to several hundred scientific articles and research reports every year. You can browse or search in our collection which contains references and links to these publications as well as other research and dissemination activities. The collection is continously updated with new and historical material.
2020
Authors
Lélis A. Carlos-Júnior Joel C. Creed Rob Marrs Rob J. Lewis Timothy P. Moulton Rafael Feijó-Lima Matthew SpencerAbstract
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Authors
Hendrik Andersen Jan Cermak Julia Fuchs Peter Knippertz Marco Gaetani Julian Quinting Sebastian Sippel Roland VogtAbstract
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Abstract
Recent discoveries have highlighted multiple mitotically and meiotically inherited alterations in gene expression that could not be explained solely by changes in the DNA sequence but were acknowledged as epigenetic. The modern view on epigenetics considers it as an integral part of genetics. Epigenetic mechanisms are encoded by genes in the genome and contribute to an essential part of genomic diversity, significantly extending its regulatory abilities. Epigenetic mechanisms involve molecular chromatin alterations through DNA methylation and histone modifications, as well as, complex non-coding RNAs and related enzyme machinery leading to changes in gene expression and resulting in changing phenotypes. In plants, epigenetic mechanisms may occur over their lifetime and across multiple generations, and can contribute substantially to phenotypic plasticity, stress responses, disease resistance, acclimation and adaptation to habitat conditions. In this review, we summarize recent advances with regards to Norway spruce epigenomics. We first consider the large size of the spruce genome that is linked to epigenetic mechanisms and why epigenomics is vitally important for spruce. Then, we discuss the molecular machinery supporting epigenetic mechanisms in Norway spruce and putative gene models involved. We presume substantial extension of gene families of epigenetic regulators and non-coding RNAs, especially in reproductive tissues. Norway spruce was the first species among forest trees in which epigenetic memory and epigenetic mechanisms were studied. The induction of an epigenetic memory during sexual reproduction and somatic embryogenesis has been described in Norway spruce. We discuss the latest results of epigenomic variation and epigenetic memory studies in Norway spruce and define the future perspectives for epigenetic studies. However, there is still a long way to decipher how the epigenetic mechanisms are involved in maintaining the stability of the spruce epigenome, how the epigenome is set to produce the epigenetic memory phenomenon and how these may result in an increased rate of adaptation to a changing environment.
Authors
Svenja B. Kroeger Daniel T. Blumstein Kenneth B. Armitage Jane Margaret Reid Julien G.A. MartinAbstract
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Authors
Selamawit Araya Kidane Beira H. Meressa Solveig Haukeland Trine Hvoslef-Eide Christer Magnusson Marjolein Couvreur Wim Bert Danny L. CoyneAbstract
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Authors
Matti Maltamo Janne Räty L. Korhonen E. Kotivuori M. Kukkonen H. Peltola J. Kangas P. PackalenAbstract
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Authors
Willem-Jan Emsens Rudy van Diggelen Camiel J. S. Aggenbach Tomáš Cajthaml Jan Frouz Agata Klimkowska Wiktor Kotowski Łukasz Kozub Yvonne Liczner Elke Seeber Hanna Marika Silvennoinen Franziska Tanneberger Jakub Vicena Mateusz Wilk Erik VerbruggenAbstract
Many of the world’s peatlands have been affected by water table drawdown and subsequent loss of organic matter. Rewetting has been proposed as a measure to restore peatland functioning and to halt carbon loss, but its effectiveness is subject to debate. An important prerequisite for peatland recovery is a return of typical microbial communities, which drive key processes. To evaluate the effect of rewetting, we investigated 13 fen peatland areas across a wide (>1500 km) longitudinal gradient in Europe, in which we compared microbial communities between drained, undrained, and rewetted sites. There was a clear difference in microbial communities between drained and undrained fens, regardless of location. Community recovery upon rewetting was substantial in the majority of sites, and predictive functional profiling suggested a concomitant recovery of biogeochemical peatland functioning. However, communities in rewetted sites were only similar to those of undrained sites when soil organic matter quality (as expressed by cellulose fractions) and quantity were still sufficiently high. We estimate that a minimum organic matter content of ca. 70% is required to enable microbial recovery. We conclude that peatland recovery after rewetting is conditional on the level of drainage-induced degradation: severely altered physicochemical peat properties may preclude complete recovery for decades.