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Establishment of a Global Network for the in Situ Conservation of Crop Wild Relatives: Status and Needs
THEMATIC BACKGROUND STUDY Establishment of a Global Network for the In Situ Conservation of Crop Wild Relatives: Status and Needs Nigel Maxted and Shelagh Kell BACKGROUND STUDY PAPER NO. 39 October 2009 COMMISSION ON GENETIC RESOURCES FOR FOOD AND AGRICULTURE ESTABLISHMENT OF A GLOBAL NETWORK FOR THE IN SITU CONSERVATION OF CROP WILD RELATIVES: STATUS AND NEEDS by *By Nigel Maxted and Shelagh Kell The content of this document is entirely the responsibility of the authors, and does not .necessarily represent the views of the FAO, or its Members 2 * School of Biosciences, University of Birmingham. Disclaimer The content of this document is entirely the responsibility of the authors, and does not necessarily represent the views of the Food and Agriculture Organization of the United Nations (FAO), or its Members. The designations employed and the presentation of material do not imply the expression of any opinion whatsoever on the part of FAO concerning legal or development status of any country, territory, city or area or of its authorities or concerning the delimitation of its frontiers or boundaries. The mention of specific companies or products of manufacturers, whether or not these have been patented, does not imply that these have been endorsed by FAO in preference to others of a similar nature that are not mentioned. CONTENTS SUMMARY 6 ACKNOWLEDGEMENTS 7 PART 1: INTRODUCTION 8 1.1 Background and scope 8 1.2 The global and local importance of crop wild relatives 10 1.3 Definition of a crop wild relative 12 1.4 Global numbers of crop -
EFFECT of WEEDY RICE (Oryza Sativa L.)
EFFECT OF WEEDY RICE (Oryza sativa L.) ON THE YIELD OF CULTIVATED RICE (Oryza sativa L.) IN GREENHOUSE AND FIELD ENVIRONMENT SALMAH BINTI TAJUDDIN UNIVERSITI SAINS MALAYSIA 2014 EFFECT OF WEEDY RICE (Oryza sativa L.) ON THE YIELD OF CULTIVATED RICE (Oryza sativa L.) IN GREENHOUSE AND FIELD ENVIRONMENT by SALMAH BINTI TAJUDDIN Thesis submitted in fulfilment of the requirements for the degree of Master of Science AUGUST 2014 ACKNOWLEDGEMENTS My postgraduate (MSc) study at the Universiti Sains Malaysia (School of Biological Sciences) was a great challenge. It was made possible with the kind assistance of many individuals, either directly or indirectly, to whom I am indebted, not all of whom are mentioned in this page. First and foremost, my deepest appreciation goes to Prof. Mashhor Mansor for his strong support, unweary supervision and motivating guidance during the course of my study. In addition, I was also trained in writing scientific papers and had the opportunity to present scientific papers in seminars and conferences. Other academicians had also given support through inspirational motivations and guidance, particularly Dr. Azmi Man, Prof. Nashriyah Mat and Dr. Asyraf Mansor, my co-supervisors, to all of whom I am very grateful. I wish to thank the staff of the Malaysian Meteorological Department Pulau Pinang for providing me the necessary meteorological data needed for my thesis. The staff of MARDI (Seberang Perai) had been very helpful in my experimental work, especially En. Awang, En. Ebnil, En. Mustafa, Pn. Norhayati and Pn. Aqilah. The staff of USM for help me solve statistics analysis problems, particularly Dr. -
Why Are Momilactones Always Associated with Biosynthetic Gene Clusters in Plants? COMMENTARY Juan Zhanga,B and Reuben J
COMMENTARY Why are momilactones always associated with biosynthetic gene clusters in plants? COMMENTARY Juan Zhanga,b and Reuben J. Petersa,1 There is an emerging realization that plant genomes intriguing hints about the distinct evolutionary pres- contain biosynthetic gene clusters (BGCs) for more sures leading to not only their assembly but also that specialized metabolism in certain cases (1). However, of BGCs in plants more generally. while horizontal gene transfer seems to drive the as- As labdane-related diterpenoids, the momilac- sembly of self-sufficient BGCs in microbes, the limita- tones require dual cyclization reactions (9). Notably, tions of strict vertical gene transmission necessitate a identification of the two relevant cyclases revealed distinct driving force for the assembly of BGCs in that the genes for these consecutively acting enzymes plants. The evidence for horizontal gene transfer of are close together in the rice genome (2). Moreover, BGCs in microbes is derived from the appearance of the only other genes in the region encode two closely homologous such loci, leading to biosynthesis of the related cytochrome P450 (CYP) monooxygenases same (or very closely related) natural products, in phy- (CYP99A2 and CYP99A3) and two short-chain alcohol logenetically distinct species. By contrast, there has dehydrogenases/reductases (SDRs) (10). The two been much less investigation of such occurrences in SDRs also are closely related, and both can catalyze plants. This is a result of many fewer examples of oxidation of the penultimate intermediate 3β-hydroxy- BGCs, as well as instances of natural products that skip syn-pimaradien-19,6β-olide to form the characteristic across phylogenetic distances in this kingdom. -
Table S1 PF00931 Species Abbreviated Species
Table S1 PF00931 Species_abbreviated Species Taxon Database 223 Acoerulea Aquilegia coerulea dicot phytozome12.1.6 152 Acomosus Ananas comosus monocot phytozome12.1.6 124 Ahalleri Arabidopsis halleri dicot phytozome12.1.6 119 Ahypochondriacus Amaranthus hypochondriacus dicot phytozome12.1.6 105 Ahypochondriacus_v2.1 Amaranthus hypochondriacus dicot phytozome12.1.6 177 Alyrata Arabidopsis lyrata dicot phytozome12.1.6 376 Aoccidentale_v0.9 Anacardium occidentale dicot phytozome12.1.6 35 Aofficinalis_V1.1 Asparagus officinalis monocot phytozome12.1.6 160 Athaliana Arabidopsis thaliana columbia dicot phytozome12.1.6 160 Athaliana_Araport11 Arabidopsis thaliana columbia dicot phytozome12.1.6 99 Atrichopoda Amborella trichopoda Amborellales phytozome12.1.6 16 Bbraunii_v2.1 Botryococcus braunii Chlorophyta phytozome12.1.6 308 Bdistachyon Brachypodium distachyon monocot phytozome12.1.6 331 BdistachyonBD21-3_v1.1 Brachypodium distachyon Bd21-3 monocot phytozome12.1.6 535 Bhybridum_v1.1 Brachypodium hybridum monocot phytozome12.1.6 114 Boleraceacapitata Brassica oleracea capitata dicot phytozome12.1.6 187 BrapaFPsc Brassica rapa FPsc dicot phytozome12.1.6 235 Bstacei Brachypodium stacei monocot phytozome12.1.6 297 Bstricta Boechera stricta dicot phytozome12.1.6 414 Bsylvaticum_v1.1 Brachypodium sylvaticum monocot phytozome12.1.6 766 Carabica_v0.5 Coffea arabica dicot phytozome12.1.6 99 Carietinum_v1.0 Cicer arietinum dicot phytozome12.1.6 342 Cclementina Citrus clementina dicot phytozome12.1.6 96 Cgrandiflora Capsella grandiflora dicot phytozome12.1.6 -
Genomes of 13 Domesticated and Wild Rice Relatives Highlight Genetic Conservation, Turnover and Innovation Across the Genus Oryza
ARTICLES https://doi.org/10.1038/s41588-018-0040-0 Corrected: Publisher Correction Genomes of 13 domesticated and wild rice relatives highlight genetic conservation, turnover and innovation across the genus Oryza Joshua C. Stein1, Yeisoo Yu2,21, Dario Copetti2,3, Derrick J. Zwickl4, Li Zhang 5, Chengjun Zhang 5, Kapeel Chougule1,2, Dongying Gao6, Aiko Iwata6, Jose Luis Goicoechea2, Sharon Wei1, Jun Wang7, Yi Liao8, Muhua Wang2,22, Julie Jacquemin2,23, Claude Becker 9, Dave Kudrna2, Jianwei Zhang2, Carlos E. M. Londono2, Xiang Song2, Seunghee Lee2, Paul Sanchez2,24, Andrea Zuccolo 2,25, Jetty S. S. Ammiraju2,26, Jayson Talag2, Ann Danowitz2, Luis F. Rivera2,27, Andrea R. Gschwend5, Christos Noutsos1, Cheng-chieh Wu10,11, Shu-min Kao10,28, Jhih-wun Zeng10, Fu-jin Wei10,29, Qiang Zhao12, Qi Feng 12, Moaine El Baidouri13, Marie-Christine Carpentier13, Eric Lasserre 13, Richard Cooke13, Daniel da Rosa Farias14, Luciano Carlos da Maia14, Railson S. dos Santos14, Kevin G. Nyberg15, Kenneth L. McNally3, Ramil Mauleon3, Nickolai Alexandrov3, Jeremy Schmutz16, Dave Flowers16, Chuanzhu Fan7, Detlef Weigel9, Kshirod K. Jena3, Thomas Wicker17, Mingsheng Chen8, Bin Han12, Robert Henry 18, Yue-ie C. Hsing10, Nori Kurata19, Antonio Costa de Oliveira14, Olivier Panaud 13, Scott A. Jackson 6, Carlos A. Machado15, Michael J. Sanderson4, Manyuan Long 5, Doreen Ware 1,20 and Rod A. Wing 2,3,4* The genus Oryza is a model system for the study of molecular evolution over time scales ranging from a few thousand to 15 million years. Using 13 reference genomes spanning the Oryza species tree, we show that despite few large-scale chromosomal rearrangements rapid species diversification is mirrored by lineage-specific emergence and turnover of many novel elements, including transposons, and potential new coding and noncoding genes. -
The Genome Sequence of African Rice (Oryza Glaberrima) and Evidence for Independent Domestication
ARTICLES OPEN The genome sequence of African rice (Oryza glaberrima) and evidence for independent domestication Muhua Wang1,16, Yeisoo Yu1,16, Georg Haberer2,16, Pradeep Reddy Marri3,16, Chuanzhu Fan1,4, Jose Luis Goicoechea1, Andrea Zuccolo5, Xiang Song1, Dave Kudrna1, Jetty S S Ammiraju1,6, Rosa Maria Cossu7, Carlos Maldonado1, Jinfeng Chen8, Seunghee Lee1, Nick Sisneros1, Kristi de Baynast1, Wolfgang Golser1, Marina Wissotski1, Woojin Kim1, Paul Sanchez1,9, Marie-Noelle Ndjiondjop10, Kayode Sanni10, Manyuan Long11, Judith Carney12, Olivier Panaud13, Thomas Wicker14, Carlos A Machado15, Mingsheng Chen8, Klaus F X Mayer2, Steve Rounsley3 & Rod A Wing1 The cultivation of rice in Africa dates back more than 3,000 years. Interestingly, African rice is not of the same origin as Asian rice (Oryza sativa L.) but rather is an entirely different species (i.e., Oryza glaberrima Steud.). Here we present a high-quality assembly and annotation of the O. glaberrima genome and detailed analyses of its evolutionary history of domestication and selection. Population genomics analyses of 20 O. glaberrima and 94 Oryza barthii accessions support the hypothesis that O. glaberrima was domesticated in a single region along the Niger river as opposed to noncentric domestication events across Africa. We detected evidence for artificial selection at a genome-wide scale, as well as with a set of O. glaberrima genes orthologous to O. sativa genes that are known to be associated with domestication, thus indicating convergent yet independent selection of a common set of genes during two geographically and culturally distinct domestication processes. O. glaberrima Steud. is an African species of rice that was inde- Here we present a high-quality assembly and annotation of the pendently domesticated from the wild progenitor O. -
Whole-Genome Sequencing of Oryza Brachyantha Reveals Mechanisms Underlying Oryza Genome Evolution
ARTICLE Received 1 Oct 2012 | Accepted 11 Feb 2013 | Published 12 Mar 2013 DOI: 10.1038/ncomms2596 OPEN Whole-genome sequencing of Oryza brachyantha reveals mechanisms underlying Oryza genome evolution Jinfeng Chen1, Quanfei Huang2, Dongying Gao3, Junyi Wang2, Yongshan Lang2, Tieyan Liu1,BoLi1, Zetao Bai1, Jose Luis Goicoechea4, Chengzhi Liang1, Chengbin Chen5, Wenli Zhang6, Shouhong Sun1, Yi Liao1, Xuemei Zhang1, Lu Yang1, Chengli Song1, Meijiao Wang1, Jinfeng Shi1, Geng Liu2, Junjie Liu2, Heling Zhou2, Weili Zhou2, Qiulin Yu2,NaAn2, Yan Chen2, Qingle Cai2, Bo Wang2, Binghang Liu2, Jiumeng Min2, Ying Huang2, Honglong Wu2, Zhenyu Li2, Yong Zhang2,YeYin2, Wenqin Song5, Jiming Jiang6, Scott A. Jackson3, Rod A. Wing4, Jun Wang2,7,8 & Mingsheng Chen1 The wild species of the genus Oryza contain a largely untapped reservoir of agronomically important genes for rice improvement. Here we report the 261-Mb de novo assembled genome sequence of Oryza brachyantha. Low activity of long-terminal repeat retrotransposons and massive internal deletions of ancient long-terminal repeat elements lead to the compact genome of Oryza brachyantha. We model 32,038 protein-coding genes in the Oryza bra- chyantha genome, of which only 70% are located in collinear positions in comparison with the rice genome. Analysing breakpoints of non-collinear genes suggests that double-strand break repair through non-homologous end joining has an important role in gene movement and erosion of collinearity in the Oryza genomes. Transition of euchromatin to heterochromatin in the rice genome is accompanied by segmental and tandem duplications, further expanded by transposable element insertions. The high-quality reference genome sequence of Oryza brachyantha provides an important resource for functional and evolutionary studies in the genus Oryza. -
Biology of RICE.Pmd
CONTENTS Foreword Preface Prologue 1. Rice as a Crop Plant ......................................................................................... 01 2. Taxonomy, Geographic Origin and Genomic Evolution.................................... 03 2.1 Taxonomy...................................................................................................... 03 2.2 Geographic origin........................................................................................... 03 2.3 Rice gene pool and species complexes.............................................................. 05 2.4 Sub-specific differentiation of the Asian cultivated rice .................................... 07 2.5 Important cultivated species/wild relatives in Southeast Asia............................ 08 2.6 Germplasm conservation ................................................................................ 10 3. Reproductive Biology....................................................................................... 12 3.1 Growth and development............................................................................... 12 3.2 Floral biology (adopted from Siddiq and Viraktamath, 2001) ........................ 17 3.3 Pollination and fertilization ............................................................................ 18 3.4 Seed dispersal ................................................................................................. 18 3.5 Seed dormancy ............................................................................................... 19 3.6 -
Rice Genomics: Over the Past Two Decades and Into the Future
Accepted Manuscript Mini Review Rice Genomics: Over the Past Two Decades and Into the Future Shuhui Song, Dongmei Tian, Zhang Zhang, Songnian Hu, Jun Yu PII: S1672-0229(19)30027-0 DOI: https://doi.org/10.1016/j.gpb.2019.01.001 Reference: GPB 331 To appear in: Genomics, Proteomics & Bioinformatics Received Date: 19 December 2018 Revised Date: 14 January 2019 Accepted Date: 23 January 2019 Please cite this article as: S. Song, D. Tian, Z. Zhang, S. Hu, J. Yu, Rice Genomics: Over the Past Two Decades and Into the Future, Genomics, Proteomics & Bioinformatics (2019), doi: https://doi.org/10.1016/j.gpb.2019.01.001 This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. Rice Genomics: Over the Past Two Decades and Into the Future Shuhui Song1,2,3,*,a, Dongmei Tian1,b, Zhang Zhang1,2,3,c, Songnian Hu2,3,d, Jun Yu2,3,*,e 1BIG Data Center, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China 2CAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China 3University of Chinese Academy of Sciences, Beijing 100049, China *Corresponding authors. E-mail: [email protected] (Yu J), [email protected] (Song S). -
A Lineage-Specific Centromere Retrotransposon in Oryza Brachyantha
The Plant Journal (2009) 60, 820–831 doi: 10.1111/j.1365-313X.2009.04005.x A lineage-specific centromere retrotransposon in Oryza brachyantha Dongying Gao1, Navdeep Gill1, Hye-Ran Kim2,3, Jason G Walling2, Wenli Zhang2, Chuanzhu Fan3, Yeisoo Yu3, Jianxin Ma1, Phillip SanMiguel4, Ning Jiang5, Zhukuan Cheng6, Rod A. Wing3, Jiming Jiang2 and Scott A. Jackson1,* 1Molecular and Evolutionary Genetics, Purdue University, 915 W. State Street, West Lafayette, IN 47907, USA, 2Department of Horticulture, University of Wisconsin-Madison, 1575 Linden Drive, Madison, WI 53706, USA, 3Arizona Genome Institute, Department of Plant Sciences, University of Arizona, 1657 E. Helen Street, Tucson, AZ 85721, USA, 4Genomics Core Facility, Purdue University, 915 W. State Street, West Lafayette, IN 47907, USA, 5Department of Horticulture, Michigan State University, East Lansing, MI 48824, USA, and 6State Key Laboratory of Plant Genomics and Center for Plant Gene Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China Received 6 June 2009; revised 28 July 2009; accepted 7 August 2009; published online 14 September 2009. *For correspondence (fax 765 496 7255; e-mail [email protected]). SUMMARY Most eukaryotic centromeres contain large quantities of repetitive DNA, such as satellite repeats and retrotransposons. Unlike most transposons in plant genomes, the centromeric retrotransposon (CR) family is conserved over long evolutionary periods among a majority of the grass species. CR elements are highly concentrated in centromeres, and are likely to play a role in centromere function. In order to study centromere evolution in the Oryza (rice) genus, we sequenced the orthologous region to centromere 8 of Oryza sativa from a related species, Oryza brachyantha. -
Molecular and Evolutionary Analysis of the Hd6 Photoperiod Sensitivity Gene Within Genus Oryza
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Springer - Publisher Connector Rice (2009) 2:56–66 DOI 10.1007/s12284-008-9019-2 Molecular and Evolutionary Analysis of the Hd6 Photoperiod Sensitivity Gene Within Genus Oryza Hiroko Yamane & Tomoko Ito & Harumi Ishikubo & Masaki Fujisawa & Harumi Yamagata & Kozue Kamiya & Yukiyo Ito & Masao Hamada & Hiroyuki Kanamori & Hiroshi Ikawa & Yuichi Katayose & Jianzhong Wu & Takuji Sasaki & Takashi Matsumoto Received: 27 April 2008 /Accepted: 31 October 2008 /Published online: 23 December 2008 # Springer Science + Business Media, LLC 2008 Abstract Heading date determines rice’s adaptation to its supported the hypothesis of independent domestication of area and cropping season. We analyzed the molecular indica and japonica rice. evolution of the Hd6 quantitative trait locus for photoperiod sensitivity in a total of 20 cultivated varieties and wild rice Keywords Oryza . Cultivated rice . Wild rice . Comparative species and found 74 polymorphic sites within its coding genomics . Heading date . Molecular evolution . Adaptation . region (1,002 bp), of which five were nonsynonymous Orthologous region . Nucleotide variation . Phylogenetic tree substitutions. Thus, natural mutations and modifications of the coding region of Hd6 within the genus Oryza have been suppressed during its evolution; this is supported by low Ka Introduction (≤0.003) and Ka/Ks (≤0.576) values between species, indicating purifying selection for a protein-coding gene. A Asian cultivated rice, Oryza sativa, is thought to have nonsynonymous substitution detected in the japonica originated from the Asian wild rice Oryza rufipogon only variety “Nipponbare” (a premature stop codon and non- about 10,000 years ago, although the place and time of its functional allele) was found within only some local domestication are still debated [8, 18, 22, 28]. -
A Host Plant Genome (Zizania Latifolia) After a Century-Long Endophyte Infection
The Plant Journal (2015) doi: 10.1111/tpj.12912 A host plant genome (Zizania latifolia) after a century-long endophyte infection Longbiao Guo1,†, Jie Qiu2,†, Zujing Han3,†, Zihong Ye4,†, Chao Chen3,†, Chuanjun Liu3, Xiufang Xin5, Chu-Yu Ye2, Ying-Ying Wang2, Hongqing Xie3, Yu Wang2, Jiandong Bao2, She Tang2, Jie Xu1, Yijie Gui2, Fei Fu2, Weidi Wang2, Xingchen Zhang2, Qianhua Zhu3, Xuanmin Guang3, Chongzhi Wang3, Haifeng Cui4, Daguang Cai6, Song Ge7, Gerald A. Tuskan8, Xiaohan Yang8, Qian Qian1, Sheng Yang He5, Jun Wang3,*, Xue-Ping Zhou9,* and Longjiang Fan2,* 1State Key Laboratory of Rice Biology, China National Rice Research Institute, Chinese Academy of Agricultural Sciences, Hangzhou 310006, China, 2Department of Agronomy & Zhejiang Key Laboratory of Crop Germplasm Resources, Zhejiang University, Hangzhou 310058, China, 3BGI-Shenzhen, Shenzhen 518083, China, 4College of Life Science, China Jiliang University, Hangzhou 310018, China, 5Howard Hughes Medical Institute, Department of Energy Plant Research Laboratory, and Department of Plant Biology, Michigan State University, East Lansing, MI 48864, USA, 6Department of Molecular Phytopathology, Christian-Albrechts-University of Kiel, D-24118, Kiel, Germany, 7State Key Laboratory of Systematic and Evolutionary Botany, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China, 8Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA, and 9State Key Laboratory of Rice Biology, Zhejiang University, Hangzhou 310058, China Received 24 January 2015; revised 26 May 2015; accepted 8 June 2015. *For correspondence (e-mails: [email protected], [email protected] or [email protected]). †These authors contributed equally to this work. SUMMARY Despite the importance of host–microbe interactions in natural ecosystems, agriculture and medicine, the impact of long-term (especially decades or longer) microbial colonization on the dynamics of host genomes is not well understood.