Suppression of a sister chromatid cohesion-defective mutant, eso1-G799D, by mutations in cohesin releaser, Wpl1. Suppression of a sister chromatid cohesion-defective.

Slides:



Advertisements
Similar presentations
BRCA2 Blue: Rad51; Green: BRCA2
Advertisements

Molecular Genetics 2010 Welcome to the course!. Molecular Genetics 2008 Welcome to the course! Describes the use of Molecular Genetics to study a range.
Have your clickers ready!. 1. In the nucleus 2. In the Golgi apparatus. 3. At the ribosomes. 4. In the DNA. 30.
BLOOM HELICASE (and BLOOM SYNDROME)
A change in the nucleotide sequence of DNA Ultimate source of genetic diversity Gene vs. Chromosome.
Membrane topology prediction of the SLC45A2 protein using TMHMM (v. 2
modified from: cell division genes activated
Figure 2 Sanger sequencing, conservation, and summary of known ACO2 mutations Sanger sequencing, conservation, and summary of known ACO2 mutations (A)
Workflow of one-step integration into any potential chromosome location. Workflow of one-step integration into any potential chromosome location. (A) After.
פחת ורווח הון סוגיות מיוחדות תהילה ששון עו"ד (רו"ח) ספטמבר 2015
Missense mutations in TNXB as a cause of VUR
Jacek Majewski  The American Journal of Human Genetics 
Multiple sequence alignment and analysis of SOFL proteins.
Figure 1. Type and distribution within KCNQ2 protein of variants in self-limiting epilepsy vs epileptic encephalopathy Type and distribution within KCNQ2.
Similarity of gene expression level (A) and nucleosome occupancy profile (B) between paralog pairs. Similarity of gene expression level (A) and nucleosome.
Mutations Any change in an organism’s DNA. Mutations in somatic cells only impact individual; mutations in gametes may impact offspring. 2 Types: A. Gene.
A Zygotic Checkpoint for Unrepaired Lesions
Deubiquitination of H2B by the SAGA complex destabilizes H2B.
Gene structures, positions of mutations, and protein domains of PRP18 paralogs in Arabidopsis. Gene structures, positions of mutations, and protein domains.
Cohesin and the Maternal Age Effect
(A) Six missense mutations in six essential genes that are not in annotated functional domains. (A) Six missense mutations in six essential genes that.
Familial history of hereditary haemorrhagic telangiectasis (HHT) of the 29-yr-old patient (•) with HHT and severe pulmonary arterial hypertension (PAH).
Genotype/Phenotype Analysis of a Photoreceptor-Specific ATP-Binding Cassette Transporter Gene, ABCR, in Stargardt Disease  Richard Alan Lewis, Noah F.
Figure 1 Dominant and recessive missense and nonsense variants in neurofilament light (NEFL)‏ Dominant and recessive missense and nonsense variants in.
Effect of the temperature-sensitive mutation hsp90G17OD on the activity of the c-src regulatory kinase Csk and on the maturation of c-srcK295M at the semirestrictive.
De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy  Lieve Claes, Jurgen Del-Favero, Berten Ceulemans, Lieven.
Splitting p63 The American Journal of Human Genetics
Sequence alignment of PHCCEx domains with secondary structure elements of the Tiam2 PHCCEx domain at the top. Sequence alignment of PHCCEx domains with.
Ataxia with Isolated Vitamin E Deficiency: Heterogeneity of Mutations and Phenotypic Variability in a Large Number of Families  Laurent Cavalier, Karim.
Understanding Human Cancer in a Fly?
Effect of dinB gene deletion on the frequency of spontaneously arisen TetR mutants in alkA tag mutS background. Effect of dinB gene deletion on the frequency.
Effect of dinB gene deletion on the frequency of spontaneously arisen TetR mutants in different genetic backgrounds. Effect of dinB gene deletion on the.
Identification of AR mutant defects in ABA, ethylene, and auxin response factors. Identification of AR mutant defects in ABA, ethylene, and auxin response.
Cohesin Releases DNA through Asymmetric ATPase-Driven Ring Opening
Analysis of GFP expression in gfp loss-of-function mutants.
Transcript length distribution resulting from different assemblies of the embryo samples across the three technologies (HiSeq, MiSeq, and PacBio). Transcript.
High-throughput ts allele sequencing.
Volume 14, Issue 9, Pages (March 2016)
Combined regulatory network with three identified modules.
GENETIC VARIATION Sources of Variation.
Cas9/gRNA-mediated gene deficiency in DF-1 cells.
Gene ontology (GO) term enrichment for significantly downregulated genes. Gene ontology (GO) term enrichment for significantly downregulated genes. Visualization.
Phylogenetic analysis and amino acid sequences comparison of HO endonucleases. Phylogenetic analysis and amino acid sequences comparison of HO endonucleases.
Figure 1 Pedigree and genetic findings
Statistics of cleavage sites and mutant-enriched sites.
Sampling locations and IDs for accessions sequenced in this study.
Coalescent analysis of nucleotide differentiation between high and low latitude samples. Coalescent analysis of nucleotide differentiation between high.
Distribution of deletions and insertions in the ade6-(GACC)7ΔT repeat.
Frequency distributions of flowering-time means for 145 accessions grown in long days. Frequency distributions of flowering-time means for 145 accessions.
Models of spreading of TCAT-like elements based on (A) retrotransposition of CR-3_TCa element. Models of spreading of TCAT-like elements based on (A) retrotransposition.
(A) yellow cDNA comparison among wild-type and ch mutants
Eff localizes in many bands and interbands of wild-type polytene chromosomes. Eff localizes in many bands and interbands of wild-type polytene chromosomes.
Frequency distribution of total leaf number for an F2 population derived from a cross of Van-0 with Ler, grown in long days. Frequency distribution of.
Spatial distribution of individual genotypes in a subpart (of size 500 grid units × 700 grid units) of the total grid after the last cycle in one replicate.
Effect of IS3 transposase on lac duplication formation.
Distribution of podocyte gene mutations in patients with genetic congenital nephrotic syndrome (CNS) and steroid–resistant nephrotic syndrome (SRNS). Distribution.
Schematic design of the SSM
Residues involved in Tim44’s interaction with Pam16 fall on one side of Tim44’s predicted N-terminal α-helix. Residues involved in Tim44’s interaction.
Comparison of rDNA histone modifications between mESCs and mNPCs.
Genetic Features of Chinese Patients with Gitelman Syndrome:
The C2H2 zinc-finger factor ztf-16 is required for ver-1 expression.
Surround integration and suppression in the direction domain.
miR-9 regulation of Pax6 expression.
Figure 2 Compound heterozygous mutations in ADAM22
–Relationship between the chiasma patterns and MI configurations of bivalent pairing with a distal FISH marker. –Relationship between the chiasma patterns.
Chromosomal Mutations
Volume 19, Issue 6, Pages (March 2009)
Information on sequenced Q. lobata adult #786.
Mapping of srt1 by BSA-seq.
Kaplan-Meier survival analysis of p53 mutation in the overall breast tumor series. Kaplan-Meier survival analysis of p53 mutation in the overall breast.
Presentation transcript:

Suppression of a sister chromatid cohesion-defective mutant, eso1-G799D, by mutations in cohesin releaser, Wpl1. Suppression of a sister chromatid cohesion-defective mutant, eso1-G799D, by mutations in cohesin releaser, Wpl1. (A) Application of the mixture sequencing strategy to eso1-G799D identified extragenic suppressors in wpl1. (B) Distribution of eso1-G799D suppressor mutations in Wpl1. Mutations are enriched in the Wapl domain of Wpl1. (C) Localization of Wpl1 missense mutations (which are conserved) in the structure of Wpl1 human homolog Wapl (Ouyang et al. 2013). Xingya Xu et al. G3 2018;8:1031-1038 ©2018 by Genetics Society of America