BAC-Based Physical Map of the Rice Genome.

Slides:



Advertisements
Similar presentations
Mapping in Arabidopsis cont…
Advertisements

Genetic and physical maps around the sex-determining M- locus of the dioecious plant asparagus Telgmann-Rauber et al
Genome sequencing. Vocabulary Bac: Bacterial Artificial Chromosome: cloning vector for yeast Pac, cosmid, fosmid, plasmid: cloning vectors for E. coli.
Genome Sequencing in the Legumes Le et al Phylogeny Major sequencing efforts Minor sequencing efforts ~14 MY ~45 MY.
Status report on gap closure of the human chromosome 5 BAC map Authentication of C5 BAC maps Map and sequence status Gap status and steps used to close.
Physical Map and Organization of Arabidopsis thaliana Chromosome 4
Copyright © 2000 American Medical Association. All rights reserved.
BrGSP: the Brassica 'A' genome sequencing project
Lisa Edelmann, Raj K. Pandita, Bernice E. Morrow 
Tracy I. George, Joanna E. Wrede, Charles D. Bangs, Athena M
The Ashkenazic Jewish Bloom Syndrome Mutation blmAsh Is Present in Non-Jewish Americans of Spanish Ancestry  Nathan A. Ellis, Susan Ciocci, Maria Proytcheva,
Der(22) Syndrome and Velo-Cardio-Facial Syndrome/DiGeorge Syndrome Share a 1.5- Mb Region of Overlap on Chromosome 22q11  B. Funke, L. Edelmann, N. McCain,
Michael Cullen, Stephen P
Reciprocal Crossovers and a Positional Preference for Strand Exchange in Recombination Events Resulting in Deletion or Duplication of Chromosome 17p11.2 
cpDNAs with large deletions accumulate in cptk1 mutants.
Evidence for Sex-Specific Risk Alleles in Autism Spectrum Disorder
Clustered 11q23 and 22q11 Breakpoints and 3:1 Meiotic Malsegregation in Multiple Unrelated t(11;22) Families  Tamim H. Shaikh, Marcia L. Budarf, Livija.
Heterozygous Submicroscopic Inversions Involving Olfactory Receptor–Gene Clusters Mediate the Recurrent t(4;8)(p16;p23) Translocation  Sabrina Giglio,
The SPCH1 Region on Human 7q31: Genomic Characterization of the Critical Interval and Localization of Translocations Associated with Speech and Language.
Genomic Rearrangements Resulting in PLP1 Deletion Occur by Nonhomologous End Joining and Cause Different Dysmyelinating Phenotypes in Males and Females 
Sequencing update of tomato chromosome 3 Chinese Academy of Sciences
Molecular Cytogenetic Evidence for a Common Breakpoint in the Largest Inverted Duplications of Chromosome 15  A.E. Wandstrat, J. Leana-Cox, L. Jenkins,
A Multicolor FISH Assay Does Not Detect DUP25 in Control Individuals or in Reported Positive Control Cells  Yanina Weiland, Jürgen Kraus, Michael R. Speicher 
A Gene Mutated in Nephronophthisis and Retinitis Pigmentosa Encodes a Novel Protein, Nephroretinin, Conserved in Evolution  Edgar Otto, Julia Hoefele,
Lan Xiong, Malgorzata Labuda, Dong-Sheng Li, Thomas J
Evidence for a Nonallelic Heterogeneity of Epidermodysplasia Verruciformis with Two Susceptibility Loci Mapped to Chromosome Regions 2p21–p24 and 17q25 
Olfactory Receptor–Gene Clusters, Genomic-Inversion Polymorphisms, and Common Chromosome Rearrangements  Sabrina Giglio, Karl W. Broman, Naomichi Matsumoto,
Airong Li, Sonia Davila, Laszlo Furu, Qi Qian, Xin Tian, Patrick S
Identification of translocations (via homeologous exchanges) in four G3 plants using BAC-FISH. Identification of translocations (via homeologous exchanges)
Segregation distortion in chromosome 3.
Disruption of Contactin 4 (CNTN4) Results in Developmental Delay and Other Features of 3p Deletion Syndrome  Thomas Fernandez, Thomas Morgan, Nicole Davis,
High-Resolution Molecular Characterization of 15q11-q13 Rearrangements by Array Comparative Genomic Hybridization (Array CGH) with Detection of Gene Dosage 
Molecular and Fluorescence In Situ Hybridization Characterization of the Breakpoints in 46 Large Supernumerary Marker 15 Chromosomes Reveals an Unexpected.
Attention Deficit Hyperactivity Disorder: Fine Mapping Supports Linkage to 5p13, 6q12, 16p13, and 17p11  Matthew N. Ogdie, Simon E. Fisher, May Yang,
Chromosome 8 cDNA microarray gene expression profile of the amplified regions of 8p11–12 in SUM-44, -52, and -225 cells versus MCF10A HME control cells.
A, genomic copy number profiles of chromosome 8 with array CGH in SUM-44, -52, and A, genomic copy number profiles of chromosome 8 with array CGH.
Volume 10, Issue 6, Pages (June 2017)
Reciprocal Crossovers and a Positional Preference for Strand Exchange in Recombination Events Resulting in Deletion or Duplication of Chromosome 17p11.2 
E.J. Hollox, J.A.L. Armour, J.C.K. Barber 
Phenotype of S-Cp1-1 and mapping of the Cp1 locus.
Yaoyu Chen, Jarod Rollins, Beverly Paigen, Xiaosong Wang 
MetaPhase clustering results on the M-Y draft metagenome assembly.
The Arabidopsis NPR1 Gene That Controls Systemic Acquired Resistance Encodes a Novel Protein Containing Ankyrin Repeats  Hui Cao, Jane Glazebrook, Joseph.
by Meru J. Sadhu, Joshua S. Bloom, Laura Day, and Leonid Kruglyak
3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome  Lionel Willatt, James Cox, John Barber, Elisabet Dachs Cabanas,
Identifying Novel Genes for Atherosclerosis through Mouse-Human Comparative Genetics  Xiaosong Wang, Naoki Ishimori, Ron Korstanje, Jarod Rollins, Beverly.
Characteristics of AtSPO11-1–Dependent sRNAs.
Mean C-to-U editing ratios for most editing sites map to a region on chromosome 6 at 122 Mb. (A) Genome scan of mean C-to-U editing for 70 editing sites.
The first two principal components for the islet gene expression data for the 181 microarray probes that map to the chromosome 6 trans-eQTL hotspot with.
Numerical analysis of cell morphology of tapetal cells in wild type.
Defective organ development in mab1 mutants.
Der(22) Syndrome and Velo-Cardio-Facial Syndrome/DiGeorge Syndrome Share a 1.5- Mb Region of Overlap on Chromosome 22q11  B. Funke, L. Edelmann, N. McCain,
Structural Variations of the Kala4 Promoters in 21 Black Rice Varieties.The Kala4 promoters of 21 black rice varieties were classified into three types.
Identification, by Homozygosity Mapping, of a Novel Locus for Autosomal Recessive Congenital Ichthyosis on Chromosome 17p, and Evidence for Further Genetic.
Genomic structure of LTBP-4 around the 3rd 8-Cys repeat.
A Gene for an Autosomal Dominant Scleroatrophic Syndrome Predisposing to Skin Cancer (Huriez Syndrome) Maps to Chromosome 4q23  Young-Ae Lee, Howard P.
Fine mapping of SRT1. Fine mapping of SRT1. To fine map the SRT1 locus, we compared the sequencing data and developed a set of InDel markers in the 5 Mb.
Multiplexed Mutagenesis Using the Csy4 System in Tomato Protoplasts.
Volume 9, Issue 2, Pages (February 2002)
Markers for Mapping by Admixture Linkage Disequilibrium in African American and Hispanic Populations  Michael W. Smith, James A. Lautenberger, Hyoung.
Representative (A) orangutan (schematic of human chromosome 7, together with the mapping position of large-insert clones, is shown alongside) and (B) Karpas.
Identification of a ufo1 Candidate Gene from the Mapping Region.
Predicted Amino Acid Sequence of the Tomato Cf-4 Protein (Thomas et al
Christa Lese Martin, Andrew Wong, Alyssa Gross, June Chung, Judy A
Gene Body CG and CHG Methylation and Suppression of Centromeric CHH Methylation are Mediated by DECREASE IN DNA METHYLATION1 in Rice  Hisataka Numa, Katsushi.
Single nucleotide polymorphism array analysis can distinguish different genetic mechanisms that lead to loss of heterozygosity (LOH). Single nucleotide.
A, heatmap of copy number alterations determined by array CGH for a panel of 79 frozen NSCLC samples. A, heatmap of copy number alterations determined.
The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic,
AtSPO11-1–Dependent sRNAs Show Enrichment at Meiotic CO-Associated DNA Motifs. AtSPO11-1–Dependent sRNAs Show Enrichment at Meiotic CO-Associated DNA Motifs.
Integrated analysis of gene expression and copy number alterations.
Presentation transcript:

BAC-Based Physical Map of the Rice Genome. BAC-Based Physical Map of the Rice Genome. The RGP genetic markers used for anchoring are listed at right in red. Next to the RGP genetic markers are the genetic positions in centimorgans. In the middle is the physical map on scale. The anchored portions are shown in red and the gaps are shown in black. At left are the contigs in order. The positions of the centromeres are shown in yellow; they are based on the RGP genetic map (Harushima et al., 1998; Saji et al., 2001). The centromeres of chromosomes 1, 6, 7, and 9 are mapped to single genetic positions at 73.4, 65.8, 49.7, and 0.8 cM, respectively. The centromeres of chromosomes 3, 4, 5, 8, 11, and 12 are mapped in genetic intervals of 0.8 cM (85.2 to 86 cM), 3.7 cM (19.6 to 23.3 cM), 1.4 cM (53.2 to 54.6 cM), 3.5 cM (50.8 to 54.3 cM), 1.1 cM (54.8 to 55.9 cM), and 3.3 cM (48.2 to 51.5 cM), respectively. The centromere of chromosome 10 is mapped to 15.4 to 15.9 cM by FISH using a centromere-specific repeat as a probe (Cheng et al., 2001). The centromere of chromosome 2 was mapped originally to 50 to 50.3 cM (Harushima et al., 1998). However, this region (∼900 kb) is located within a single contig with a physical-to-genetic distance ratio of 369 kb/cM, whereas the neighboring contig has severely suppressed recombination (>1 Mb/cM). Therefore, we have included 50 to 54.6 cM as the centromeric region for chromosome 2. Mingsheng Chen et al. Plant Cell 2002;14:537-545 ©2002 by American Society of Plant Biologists