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Featured researches published by Yao-Cheng Lin.


Nature | 2008

The genome of Laccaria bicolor provides insights into mycorrhizal symbiosis

Francis L. Martin; Andrea Aerts; Dag Ahrén; Annick Brun; E. G. J. Danchin; F. Duchaussoy; J. Gibon; Annegret Kohler; Erika Lindquist; V. Pereda; Asaf Salamov; Harris Shapiro; Jan Wuyts; D. Blaudez; M. Buée; P. Brokstein; Björn Canbäck; D. Cohen; P. E. Courty; P. M. Coutinho; Christine Delaruelle; John C. Detter; A. Deveau; Stephen P. DiFazio; Sébastien Duplessis; L. Fraissinet-Tachet; E. Lucic; P. Frey-Klett; C. Fourrey; Ivo Feussner

Mycorrhizal symbioses—the union of roots and soil fungi—are universal in terrestrial ecosystems and may have been fundamental to land colonization by plants. Boreal, temperate and montane forests all depend on ectomycorrhizae. Identification of the primary factors that regulate symbiotic development and metabolic activity will therefore open the door to understanding the role of ectomycorrhizae in plant development and physiology, allowing the full ecological significance of this symbiosis to be explored. Here we report the genome sequence of the ectomycorrhizal basidiomycete Laccaria bicolor (Fig. 1) and highlight gene sets involved in rhizosphere colonization and symbiosis. This 65-megabase genome assembly contains ∼20,000 predicted protein-encoding genes and a very large number of transposons and repeated sequences. We detected unexpected genomic features, most notably a battery of effector-type small secreted proteins (SSPs) with unknown function, several of which are only expressed in symbiotic tissues. The most highly expressed SSP accumulates in the proliferating hyphae colonizing the host root. The ectomycorrhizae-specific SSPs probably have a decisive role in the establishment of the symbiosis. The unexpected observation that the genome of L. bicolor lacks carbohydrate-active enzymes involved in degradation of plant cell walls, but maintains the ability to degrade non-plant cell wall polysaccharides, reveals the dual saprotrophic and biotrophic lifestyle of the mycorrhizal fungus that enables it to grow within both soil and living plant roots. The predicted gene inventory of the L. bicolor genome, therefore, points to previously unknown mechanisms of symbiosis operating in biotrophic mycorrhizal fungi. The availability of this genome provides an unparalleled opportunity to develop a deeper understanding of the processes by which symbionts interact with plants within their ecosystem to perform vital functions in the carbon and nitrogen cycles that are fundamental to sustainable plant productivity.


Nature | 2013

The Norway spruce genome sequence and conifer genome evolution

Björn Nystedt; Nathaniel R. Street; Anna Wetterbom; Andrea Zuccolo; Yao-Cheng Lin; Douglas G. Scofield; Francesco Vezzi; Nicolas Delhomme; Stefania Giacomello; Andrey Alexeyenko; Riccardo Vicedomini; Kristoffer Sahlin; Ellen Sherwood; Malin Elfstrand; Lydia Gramzow; Kristina Holmberg; Jimmie Hällman; Olivier Keech; Lisa Klasson; Maxim Koriabine; Melis Kucukoglu; Max Käller; Johannes Luthman; Fredrik Lysholm; Totte Niittylä; Åke Olson; Nemanja Rilakovic; Carol Ritland; Josep A. Rosselló; Juliana Stival Sena

Conifers have dominated forests for more than 200 million years and are of huge ecological and economic importance. Here we present the draft assembly of the 20-gigabase genome of Norway spruce (Picea abies), the first available for any gymnosperm. The number of well-supported genes (28,354) is similar to the >100 times smaller genome of Arabidopsis thaliana, and there is no evidence of a recent whole-genome duplication in the gymnosperm lineage. Instead, the large genome size seems to result from the slow and steady accumulation of a diverse set of long-terminal repeat transposable elements, possibly owing to the lack of an efficient elimination mechanism. Comparative sequencing of Pinus sylvestris, Abies sibirica, Juniperus communis, Taxus baccata and Gnetum gnemon reveals that the transposable element diversity is shared among extant conifers. Expression of 24-nucleotide small RNAs, previously implicated in transposable element silencing, is tissue-specific and much lower than in other plants. We further identify numerous long (>10,000 base pairs) introns, gene-like fragments, uncharacterized long non-coding RNAs and short RNAs. This opens up new genomic avenues for conifer forestry and breeding.


Proceedings of the National Academy of Sciences of the United States of America | 2011

Obligate biotrophy features unraveled by the genomic analysis of rust fungi

Sébastien Duplessis; Christina A. Cuomo; Yao-Cheng Lin; Andrea Aerts; Emilie Tisserant; Claire Veneault-Fourrey; David L. Joly; Stéphane Hacquard; Joelle Amselem; Brandi L. Cantarel; Readman Chiu; Pedro M. Coutinho; Nicolas Feau; Matthew A. Field; Pascal Frey; Eric Gelhaye; Jonathan M. Goldberg; Manfred Grabherr; Chinnappa D. Kodira; Annegret Kohler; Ursula Kües; Erika Lindquist; Susan Lucas; Rohit Mago; Evan Mauceli; Emmanuelle Morin; Claude Murat; Jasmyn Pangilinan; Robert F. Park; Matthew Pearson

Rust fungi are some of the most devastating pathogens of crop plants. They are obligate biotrophs, which extract nutrients only from living plant tissues and cannot grow apart from their hosts. Their lifestyle has slowed the dissection of molecular mechanisms underlying host invasion and avoidance or suppression of plant innate immunity. We sequenced the 101-Mb genome of Melampsora larici-populina, the causal agent of poplar leaf rust, and the 89-Mb genome of Puccinia graminis f. sp. tritici, the causal agent of wheat and barley stem rust. We then compared the 16,399 predicted proteins of M. larici-populina with the 17,773 predicted proteins of P. graminis f. sp tritici. Genomic features related to their obligate biotrophic lifestyle include expanded lineage-specific gene families, a large repertoire of effector-like small secreted proteins, impaired nitrogen and sulfur assimilation pathways, and expanded families of amino acid and oligopeptide membrane transporters. The dramatic up-regulation of transcripts coding for small secreted proteins, secreted hydrolytic enzymes, and transporters in planta suggests that they play a role in host infection and nutrient acquisition. Some of these genomic hallmarks are mirrored in the genomes of other microbial eukaryotes that have independently evolved to infect plants, indicating convergent adaptation to a biotrophic existence inside plant cells.


Nature Biotechnology | 2009

Genome sequence of the recombinant protein production host Pichia pastoris.

Kristof De Schutter; Yao-Cheng Lin; Petra Tiels; Annelies Van Hecke; Sascha Glinka; Jacqueline Weber-Lehmann; Pierre Rouzé; Yves Van de Peer; Nico Callewaert

The methylotrophic yeast Pichia pastoris is widely used for the production of proteins and as a model organism for studying peroxisomal biogenesis and methanol assimilation. P. pastoris strains capable of human-type N-glycosylation are now available, which increases the utility of this organism for biopharmaceutical production. Despite its biotechnological importance, relatively few genetic tools or engineered strains have been generated for P. pastoris. To facilitate progress in these areas, we present the 9.43 Mbp genomic sequence of the GS115 strain of P. pastoris. We also provide manually curated annotation for its 5,313 protein-coding genes.


Proceedings of the National Academy of Sciences of the United States of America | 2011

Obligate Biotrophy Features Unraveled by the Genomic Analysis of the Rust Fungi, Melampsora larici-populina and Puccinia graminis f. sp. tritici

Sébastien Duplessis; Christina A. Cuomo; Yao-Cheng Lin; Andrea Aerts; Emilie Tisserant; Claire Veneault-Fourrey; David L. Joly; Stéphane Hacquard; Joelle Amselem; Brandi L. Cantarel; Readman Chiu; Pedro Couthinho; Nicolas Feau; Matthew A. Field; Pascal Frey; Eric Gelhaye; Jonathan M. Goldberg; Manfred Grabherr; Chinnappa D. Kodira; Annegret Kohler; Ursula Kües; Erika Lindquist; Susan Lucas; Rohit Mago; Evan Mauceli; Emmanuelle Morin; Claude Murat; Jasmyn Pangilinan; Robert F. Park; Matthew Pearson

Rust fungi are some of the most devastating pathogens of crop plants. They are obligate biotrophs, which extract nutrients only from living plant tissues and cannot grow apart from their hosts. Their lifestyle has slowed the dissection of molecular mechanisms underlying host invasion and avoidance or suppression of plant innate immunity. We sequenced the 101-Mb genome of Melampsora larici-populina, the causal agent of poplar leaf rust, and the 89-Mb genome of Puccinia graminis f. sp. tritici, the causal agent of wheat and barley stem rust. We then compared the 16,399 predicted proteins of M. larici-populina with the 17,773 predicted proteins of P. graminis f. sp tritici. Genomic features related to their obligate biotrophic lifestyle include expanded lineage-specific gene families, a large repertoire of effector-like small secreted proteins, impaired nitrogen and sulfur assimilation pathways, and expanded families of amino acid and oligopeptide membrane transporters. The dramatic up-regulation of transcripts coding for small secreted proteins, secreted hydrolytic enzymes, and transporters in planta suggests that they play a role in host infection and nutrient acquisition. Some of these genomic hallmarks are mirrored in the genomes of other microbial eukaryotes that have independently evolved to infect plants, indicating convergent adaptation to a biotrophic existence inside plant cells.


Nature | 2013

Pan genome of the phytoplankton Emiliania underpins its global distribution

Betsy A. Read; Jessica Kegel; Mary J. Klute; Alan Kuo; Stephane C. Lefebvre; Florian Maumus; Christoph Mayer; John P. Miller; Adam Monier; Asaf Salamov; Jeremy R. Young; Maria Aguilar; Jean-Michel Claverie; Stephan Frickenhaus; Karina Gonzalez; Emily K. Herman; Yao-Cheng Lin; Johnathan A. Napier; Hiroyuki Ogata; Analissa F Sarno; Jeremy Shmutz; Declan C. Schroeder; Frederic Verret; Peter von Dassow; Klaus Valentin; Yves Van de Peer; Glen L. Wheeler; Emiliana Huxleyi; Joel B. Dacks; Charles F. Delwiche

Coccolithophores have influenced the global climate for over 200 million years. These marine phytoplankton can account for 20 per cent of total carbon fixation in some systems. They form blooms that can occupy hundreds of thousands of square kilometres and are distinguished by their elegantly sculpted calcium carbonate exoskeletons (coccoliths), rendering them visible from space. Although coccolithophores export carbon in the form of organic matter and calcite to the sea floor, they also release CO2 in the calcification process. Hence, they have a complex influence on the carbon cycle, driving either CO2 production or uptake, sequestration and export to the deep ocean. Here we report the first haptophyte reference genome, from the coccolithophore Emiliania huxleyi strain CCMP1516, and sequences from 13 additional isolates. Our analyses reveal a pan genome (core genes plus genes distributed variably between strains) probably supported by an atypical complement of repetitive sequence in the genome. Comparisons across strains demonstrate that E. huxleyi, which has long been considered a single species, harbours extensive genome variability reflected in different metabolic repertoires. Genome variability within this species complex seems to underpin its capacity both to thrive in habitats ranging from the equator to the subarctic and to form large-scale episodic blooms under a wide variety of environmental conditions.


New Phytologist | 2012

Insight into trade???off between wood decay and parasitism from the genome of a fungal forest pathogen

Åke Olson; Andrea Aerts; Fred O. Asiegbu; Lassaad Belbahri; Ourdia Bouzid; Anders Broberg; Björn Canbäck; Pedro M. Coutinho; Dan Cullen; Kerstin Dalman; Giuliana Deflorio; Linda T.A. van Diepen; Christophe Dunand; Sébastien Duplessis; Mikael Brandström Durling; Paolo Gonthier; Jane Grimwood; Carl Gunnar Fossdal; David Hansson; Bernard Henrissat; Ari M. Hietala; Kajsa Himmelstrand; Dirk Hoffmeister; Nils Högberg; Timothy Y. James; Magnus Karlsson; Annegret Kohler; Ursula Kües; Yong-Hwan Lee; Yao-Cheng Lin

Parasitism and saprotrophic wood decay are two fungal strategies fundamental for succession and nutrient cycling in forest ecosystems. An opportunity to assess the trade-off between these strategies is provided by the forest pathogen and wood decayer Heterobasidion annosum sensu lato. We report the annotated genome sequence and transcript profiling, as well as the quantitative trait loci mapping, of one member of the species complex: H. irregulare. Quantitative trait loci critical for pathogenicity, and rich in transposable elements, orphan and secreted genes, were identified. A wide range of cellulose-degrading enzymes are expressed during wood decay. By contrast, pathogenic interaction between H. irregulare and pine engages fewer carbohydrate-active enzymes, but involves an increase in pectinolytic enzymes, transcription modules for oxidative stress and secondary metabolite production. Our results show a trade-off in terms of constrained carbohydrate decomposition and membrane transport capacity during interaction with living hosts. Our findings establish that saprotrophic wood decay and necrotrophic parasitism involve two distinct, yet overlapping, processes.


Nature | 2016

The genome of the seagrass Zostera marina reveals angiosperm adaptation to the sea

Jeanine L. Olsen; Pierre Rouzé; Bram Verhelst; Yao-Cheng Lin; Till Bayer; Jonas Collén; Emanuela Dattolo; Emanuele De Paoli; Simon M. Dittami; Florian Maumus; Gurvan Michel; Anna R. Kersting; Chiara Lauritano; Rolf Lohaus; Mats Töpel; Thierry Tonon; Kevin Vanneste; Mojgan Amirebrahimi; Janina Brakel; Christoffer Boström; Mansi Chovatia; Jane Grimwood; Jerry Jenkins; Alexander Jueterbock; Amy Mraz; Wytze T. Stam; Hope Tice; Erich Bornberg-Bauer; Pamela J. Green; Gareth A. Pearson

Seagrasses colonized the sea on at least three independent occasions to form the basis of one of the most productive and widespread coastal ecosystems on the planet. Here we report the genome of Zostera marina (L.), the first, to our knowledge, marine angiosperm to be fully sequenced. This reveals unique insights into the genomic losses and gains involved in achieving the structural and physiological adaptations required for its marine lifestyle, arguably the most severe habitat shift ever accomplished by flowering plants. Key angiosperm innovations that were lost include the entire repertoire of stomatal genes, genes involved in the synthesis of terpenoids and ethylene signalling, and genes for ultraviolet protection and phytochromes for far-red sensing. Seagrasses have also regained functions enabling them to adjust to full salinity. Their cell walls contain all of the polysaccharides typical of land plants, but also contain polyanionic, low-methylated pectins and sulfated galactans, a feature shared with the cell walls of all macroalgae and that is important for ion homoeostasis, nutrient uptake and O2/CO2 exchange through leaf epidermal cells. The Z. marina genome resource will markedly advance a wide range of functional ecological studies from adaptation of marine ecosystems under climate warming, to unravelling the mechanisms of osmoregulation under high salinities that may further inform our understanding of the evolution of salt tolerance in crop plants.


Nature Communications | 2014

Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations

Yao-Cheng Lin; Morgane Boone; Leander Meuris; Irma Lemmens; Nadine Van Roy; Arne Soete; Joke Reumers; Matthieu Moisse; Stephane Plaisance; Radoje Drmanac; Jason Chen; Franki Speleman; Diether Lambrechts; Yves Van de Peer; Jan Tavernier; Nico Callewaert

The HEK293 human cell lineage is widely used in cell biology and biotechnology. Here we use whole-genome resequencing of six 293 cell lines to study the dynamics of this aneuploid genome in response to the manipulations used to generate common 293 cell derivatives, such as transformation and stable clone generation (293T); suspension growth adaptation (293S); and cytotoxic lectin selection (293SG). Remarkably, we observe that copy number alteration detection could identify the genomic region that enabled cell survival under selective conditions (i.c. ricin selection). Furthermore, we present methods to detect human/vector genome breakpoints and a user-friendly visualization tool for the 293 genome data. We also establish that the genome structure composition is in steady state for most of these cell lines when standard cell culturing conditions are used. This resource enables novel and more informed studies with 293 cells, and we will distribute the sequenced cell lines to this effect.


Developmental Cell | 2012

GOLVEN Secretory Peptides Regulate Auxin Carrier Turnover during Plant Gravitropic Responses

Ryan Whitford; Ana Fernandez; Ricardo Tejos; Amparo Cuéllar Pérez; Jürgen Kleine-Vehn; Steffen Vanneste; Andrzej Drozdzecki; Johannes Leitner; Lindy Abas; Maarten Aerts; Kurt Hoogewijs; Pawel Radoslaw Baster; Ruth De Groodt; Yao-Cheng Lin; Veronique Storme; Yves Van de Peer; Tom Beeckman; Annemieke Madder; Bart Devreese; Christian Luschnig; Jiri Friml; Pierre Hilson

Growth and development are coordinated by an array of intercellular communications. Known plant signaling molecules include phytohormones and hormone peptides. Although both classes can be implicated in the same developmental processes, little is known about the interplay between phytohormone action and peptide signaling within the cellular microenvironment. We show that genes coding for small secretory peptides, designated GOLVEN (GLV), modulate the distribution of the phytohormone auxin. The deregulation of the GLV function impairs the formation of auxin gradients and alters the reorientation of shoots and roots after a gravity stimulus. Specifically, the GLV signal modulates the trafficking dynamics of the auxin efflux carrier PIN-FORMED2 involved in root tropic responses and meristem organization. Our work links the local action of secretory peptides with phytohormone transport.

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Andrea Aerts

United States Department of Energy

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Sébastien Duplessis

Institut national de la recherche agronomique

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Ursula Kües

University of Göttingen

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