FANCM promotes class I interfering crossovers and suppresses class II non-interfering crossovers in wheat meiosis

[1]  Paul D. Shaw,et al.  An Induced Mutation in HvRECQL4 Increases the Overall Recombination and Restores Fertility in a Barley HvMLH3 Mutant Background , 2021, Frontiers in Plant Science.

[2]  I. Henderson,et al.  Crossover-active regions of the wheat genome are distinguished by DMC1, the chromosome axis, H3K27me3, and signatures of adaptation , 2021, Genome research.

[3]  Zhukuan Cheng,et al.  Replication protein A large subunit (RPA1a) limits chiasma formation during rice meiosis. , 2021, Plant physiology.

[4]  John A. Fozard,et al.  Diffusion-mediated HEI10 coarsening can explain meiotic crossover positioning in Arabidopsis , 2021, Nature Communications.

[5]  J. Higgins,et al.  ZYP1 is required for obligate cross-over formation and cross-over interference in Arabidopsis , 2021, Proceedings of the National Academy of Sciences.

[6]  Qichao Lian,et al.  The synaptonemal complex imposes crossover interference and heterochiasmy in Arabidopsis , 2021, Proceedings of the National Academy of Sciences.

[7]  Hyun Seob Cho,et al.  HIGH CROSSOVER RATE1 encodes PROTEIN PHOSPHATASE X1 and restricts meiotic crossovers in Arabidopsis , 2021, Nature Plants.

[8]  I. Henderson,et al.  Distal Bias of Meiotic Crossovers in Hexaploid Bread Wheat Reflects Spatio-Temporal Asymmetry of the Meiotic Program , 2021, Frontiers in Plant Science.

[9]  Xiang Li,et al.  Fanconi Anemia Ortholog FANCM Regulates Meiotic Crossover Distribution in Plants. , 2021, Plant physiology.

[10]  D. Leshkowitz,et al.  Redistribution of Meiotic Crossovers Along Wheat Chromosomes by Virus-Induced Gene Silencing , 2021, Frontiers in Plant Science.

[11]  I. Henderson,et al.  MutS homologue 4 and MutS homologue 5 Maintain the Obligate Crossover in Wheat Despite Stepwise Gene Loss following Polyploidization1[CC-BY] , 2020, Plant Physiology.

[12]  N. M. Hollingsworth,et al.  DNA Helicase Mph1FANCM Ensures Meiotic Recombination between Parental Chromosomes by Dissociating Precocious Displacement Loops. , 2020, Developmental cell.

[13]  J. Higgins,et al.  A Cytological Analysis of Wheat Meiosis Targeted by Virus-Induced Gene Silencing (VIGS). , 2020, Methods in molecular biology.

[14]  Wenli Zhang,et al.  The bread wheat epigenomic map reveals distinct chromatin architectural and evolutionary features of functional genetic elements , 2019, Genome Biology.

[15]  Bernardo J. Clavijo,et al.  Analysis of the recombination landscape of hexaploid bread wheat reveals genes controlling recombination and gene conversion frequency , 2019, Genome Biology.

[16]  Arthur T. O. Melo,et al.  Durum wheat genome highlights past domestication signatures and future improvement targets , 2019, Nature Genetics.

[17]  Jonathan D. G. Jones,et al.  Shifting the limits in wheat research and breeding using a fully annotated reference genome , 2018, Science.

[18]  K. Jordan,et al.  The genetic architecture of genome‐wide recombination rate variation in allopolyploid wheat revealed by nested association mapping , 2018, The Plant journal : for cell and molecular biology.

[19]  G. Droc,et al.  Unleashing meiotic crossovers in crops , 2018, bioRxiv.

[20]  G. Copenhaver,et al.  Meiotic Recombination: Mixing It Up in Plants. , 2018, Annual review of plant biology.

[21]  D. Charif,et al.  FANCM Limits Meiotic Crossovers in Brassica Crops , 2018, Front. Plant Sci..

[22]  Gerhard Dürnberger,et al.  Affinity proteomics reveals extensive phosphorylation of the Brassica chromosome axis protein ASY1 and a network of associated proteins at prophase I of meiosis , 2017, The Plant journal : for cell and molecular biology.

[23]  R. Mercier,et al.  Unleashing meiotic crossovers in hybrid plants , 2017, Proceedings of the National Academy of Sciences.

[24]  B. Servin,et al.  High-Resolution Mapping of Crossover Events in the Hexaploid Wheat Genome Suggests a Universal Recombination Mechanism , 2017, Genetics.

[25]  R. Martienssen,et al.  Natural variation and dosage of the HEI10 meiotic E3 ligase control Arabidopsis crossover recombination , 2017, Genes & development.

[26]  F. C. H. Franklin,et al.  Understanding and Manipulating Meiotic Recombination in Plants[OPEN] , 2017, Plant Physiology.

[27]  Leah Clissold,et al.  Uncovering hidden variation in polyploid wheat , 2017, Proceedings of the National Academy of Sciences.

[28]  J. Higgins,et al.  CENH3 morphogenesis reveals dynamic centromere associations during synaptonemal complex formation and the progression through male meiosis in hexaploid wheat , 2017, The Plant journal : for cell and molecular biology.

[29]  F. Han,et al.  De Novo Centromere Formation and Centromeric Sequence Expansion in Wheat and its Wide Hybrids , 2016, PLoS genetics.

[30]  L. Chelysheva,et al.  A DNA topoisomerase VI–like complex initiates meiotic recombination , 2016, Science.

[31]  Teresa A. Webster,et al.  High‐density SNP genotyping array for hexaploid wheat and its secondary and tertiary gene pool , 2015, Plant biotechnology journal.

[32]  L. Chelysheva,et al.  AAA-ATPase FIDGETIN-LIKE 1 and Helicase FANCM Antagonize Meiotic Crossovers by Distinct Mechanisms , 2015, PLoS genetics.

[33]  M. Grelon,et al.  The molecular biology of meiosis in plants. , 2015, Annual review of plant biology.

[34]  Jelle Van Leene,et al.  Multiple mechanisms limit meiotic crossovers: TOP3α and two BLM homologs antagonize crossovers in parallel to FANCM , 2015, Proceedings of the National Academy of Sciences.

[35]  Krystyna A. Kelly,et al.  Juxtaposition of heterozygous and homozygous regions causes reciprocal crossover remodelling via interference during Arabidopsis meiosis , 2015, eLife.

[36]  Hadi Quesneville,et al.  Structural and functional partitioning of bread wheat chromosome 3B , 2014, Science.

[37]  R. Mercier,et al.  FANCM-associated proteins MHF1 and MHF2, but not the other Fanconi anemia factors, limit meiotic crossovers , 2014, Nucleic acids research.

[38]  Zujun Yang,et al.  Oligonucleotides replacing the roles of repetitive sequences pAs1, pSc119.2, pTa-535, pTa71, CCS1, and pAWRC.1 for FISH analysis , 2014, Journal of Applied Genetics.

[39]  J. Higgins.  Analyzing meiosis in barley. , 2013, Methods in molecular biology.

[40]  M. Novatchkova,et al.  The Arabidopsis HEI10 Is a New ZMM Protein Related to Zip3 , 2012, PLoS genetics.

[41]  G. Copenhaver,et al.  FANCM Limits Meiotic Crossovers , 2012, Science.

[42]  J. Higgins,et al.  The Fanconi Anemia Ortholog FANCM Ensures Ordered Homologous Recombination in Both Somatic and Meiotic Cells in Arabidopsis[W] , 2012, Plant Cell.

[43]  Chenggui Han,et al.  A High Throughput Barley Stripe Mosaic Virus Vector for Virus Induced Gene Silencing in Monocots and Dicots , 2011, PloS one.

[44]  E. Sanchez-Moran,et al.  Pathways to meiotic recombination in Arabidopsis thaliana. , 2011, The New phytologist.

[45]  J. Slovin,et al.  A simplified method for differential staining of aborted and non-aborted pollen grains , 2010 .

[46]  Luke E. Berchowitz,et al.  Genetic Interference: Don’t Stand So Close to Me , 2010, Current genomics.

[47]  P. Shewry,et al.  Diversity of agronomic and morphological traits in a mutant population of bread wheat studied in the Healthgrain program , 2010, Euphytica.

[48]  E. Sanchez-Moran,et al.  Replication protein A (AtRPA1a) is required for class I crossover formation but is dispensable for meiotic DNA break repair , 2009, The EMBO journal.

[49]  J. Higgins,et al.  AtMSH5 partners AtMSH4 in the class I meiotic crossover pathway in Arabidopsis thaliana, but is not required for synapsis. , 2008, The Plant journal : for cell and molecular biology.

[50]  L. Steinmetz,et al.  High-resolution mapping of meiotic crossovers and non-crossovers in yeast , 2008, Nature.

[51]  J. Higgins,et al.  Expression and functional analysis of AtMUS81 in Arabidopsis meiosis reveals a role in the second pathway of crossing-over. , 2008, The Plant journal : for cell and molecular biology.

[52]  Luke E. Berchowitz,et al.  The Role of AtMUS81 in Interference-Insensitive Crossovers in A. thaliana , 2007, PLoS genetics.

[53]  F. C. H. Franklin,et al.  Meiotic Crossing-over: Obligation and Interference , 2006, Cell.

[54]  E. Sanchez-Moran,et al.  The Arabidopsis synaptonemal complex protein ZYP1 is required for chromosome synapsis and normal fidelity of crossing over. , 2005, Genes & development.

[55]  Hong Ma,et al.  The AtRAD51C Gene Is Required for Normal Meiotic Chromosome Synapsis and Double-Stranded Break Repair in Arabidopsis1 , 2005, Plant Physiology.

[56]  J. Higgins,et al.  The Arabidopsis MutS homolog AtMSH4 functions at an early step in recombination: evidence for two classes of recombination in Arabidopsis. , 2004, Genes & development.

[57]  N. Kleckner,et al.  Crossover/Noncrossover Differentiation, Synaptonemal Complex Formation, and Regulatory Surveillance at the Leptotene/Zygotene Transition of Meiosis , 2004, Cell.

[58]  R. Holland,et al.  Don't Stand So Close to Me , 2004, Psychological science.

[59]  D. Sandhu,et al.  Demarcating the gene-rich regions of the wheat genome. , 2004, Nucleic acids research.

[60]  C. Makaroff,et al.  The meiotic protein SWI1 is required for axial element formation and recombination initiation in Arabidopsis , 2003, Development.

[61]  F. Franklin,et al.  Asy1, a protein required for meiotic chromosome synapsis, localizes to axis-associated chromatin in Arabidopsis and Brassica , 2002, Journal of Cell Science.

[62]  S. Keeney,et al.  Meiosis-Specific DNA Double-Strand Breaks Are Catalyzed by Spo11, a Member of a Widely Conserved Protein Family , 1997, Cell.