The trouble with binding sites Joe Pearson 1/11/10.

Slides:



Advertisements
Similar presentations
Exploiting transcription factor binding site clustering to identify cis-regulatory modules involved in pattern formation in the Drosophila genome ECS289A.
Advertisements

Outline Questions from last lecture? P. 40 questions on Pax6 gene Mechanism of Transcription Activation –Transcription Regulatory elements Comparison between.
1/25/10 runt and engrailed-dependent specification of midline glia.
Combined analysis of ChIP- chip data and sequence data Harbison et al. CS 466 Saurabh Sinha.
Gene regulation in cancer 11/14/07. Overview The hallmark of cancer is uncontrolled cell proliferation. Oncogenes code for proteins that help to regulate.
Speaker: HU Xue-Jia Supervisor: WU Yun-Dong Date: 19/12/2013.
Identification and Comparison of Midline Cis-Regulatory Elements.
Candidate Genes Interact with Sim::Tgo Yu-Chi Chen December 19 th, 2006 PART 1 (August-October)
Fusion cell gene profiling Identify mbo and CG15252 enhancer Molecular mechanism of target gene regulation by Dys::Tgo Dys::Tgo activation of CG13196 Dys:Tgo.
Microarrays and Cancer Segal et al. CS 466 Saurabh Sinha.
1.Notch signaling and midline cell development 2.Neuron/glia interactions; nrx.
Transcriptional regulation of tracheal fusion cell gene expression Isolate enhancer of three fusion cell expressed genes: dys, CG15252, CG13196 Identify.
Genes. Eukaryotic Protein-Coding Gene Structure codingnon-coding.
A modest collection of Midline CRMs Joe Pearson Lab Meeting 8/25/08.
Building a functional nervous system Immature CNS Cells Motorneurons Neurosecretory cells Glia Interneurons Cell fate determination Cell migration Apoptosis.
Rhomboid MLE regulation by Sim:Tgo and Su(H) 8/24/09.
1 Predicting Gene Expression from Sequence Michael A. Beer and Saeed Tavazoie Cell 117, (16 April 2004)
CS 374: Relating the Genetic Code to Gene Expression Sandeep Chinchali.
Cis-regultory module 10/24/07. TFs often work synergistically (Harbison 2004)
Computational Molecular Biology Biochem 218 – BioMedical Informatics Gene Regulatory.
* only 17% of SNPs implicated in freshwater adaptation map to coding sequences Many, many mapping studies find prevalent noncoding QTLs.
Lab Meeting Generation of CNS Neuronal and Glial Diversity Immature CNS Cells Interneurons Motorneurons Neurosecretory cells Glia.
Identification of SIP1-modulated genes during the epithelial-to-mesenchymal transition and interactions with KLF factors in EMT control Benjamin Koopmansch.
Regulation of Gene Expression Chapter 18. Warm Up Explain the difference between a missense and a nonsense mutation. What is a silent mutation? QUIZ TOMORROW:
YUEMIN DING Neuro-oncology Group Department of Molecular Neuroscience
Gene repression and activation
A Systems Approach to Infectious Disease Research: Influenza Develop a molecular network model of the interaction between influenza virus and the innate.
Molecular Basis for Relationship between Genotype and Phenotype DNA RNA protein genotype function organism phenotype DNA sequence amino acid sequence transcription.
Inference with Gene Expression and Sequence Data BMI/CS 776 Mark Craven April 2002.
Outline Molecular Cell Biology Assessment Review from last lecture Role of nucleoporins in transcription Activators and Repressors Epigenetic mechanisms.
Transcriptional Enhancers Looking out for the genes and each other Sridhar Hannenhalli Department of Cell Biology and Molecular Genetics Center for Bioinformatics.
Enhancers and 3D genomics Noam Bar RESEARCH METHODS IN COMPUTATIONAL BIOLOGY.
Evaluation of count scores for weight matrix motifs Project Presentation for CS598SS Hong Cheng and Qiaozhu Mei.
Prototypical eukaryotic gene
Background for Molecular Biology of Lactase Persistence
Stories arising… Joe Pearson 5/10/2009.
more regulating gene expression
binding sites 58 of the 473 unambiguously assigned phosphorylation sites are predicted by Scansite to be sites for binding. 50 of these correspond.
Nat. Rev. Clin. Oncol. doi: /nrclinonc
A Time to Divide: Does the Circadian Clock Control Cell Cycle?
Relationship between Genotype and Phenotype
A Zero-Knowledge Based Introduction to Biology
From Prescription to Transcription: Genome Sequence as Drug Target
Structural Rules and Complex Regulatory Circuitry Constrain Expression of a Notch- and EGFR-Regulated Eye Enhancer  Christina I. Swanson, Nicole C. Evans,
Genomic Regulatory Networks and Animal Development
Figure 3 Differences in renal cell carcinoma (RCC) between genders
Even-skipped gene regulation
Bearded Family Members Inhibit Neuralized-Mediated Endocytosis and Signaling Activity of Delta in Drosophila  Allison J. Bardin, François Schweisguth 
Control of splicing. Control of splicing. Cis acting elements, such as exon splicing enhancer sequences (ESE), exon splicing silencers (ESS), intron splicing.
In collaboration with Mikkelsen Lab
Volume 17, Issue 5, Pages (October 2016)
Nat. Rev. Gastroenterol. Hepatol. doi: /nrgastro
Volume 111, Issue 5, Pages (November 2002)
Novel p53 target genes identified by RNA-Seq, pSILAC and ChIP-Seq.
The Noncanonical Binding Site of the MED-1 GATA Factor Defines Differentially Regulated Target Genes in the C. elegans Mesendoderm  Gina Broitman-Maduro,
Volume 5, Issue 3, Pages (March 2000)
Rapid Evolutionary Rewiring of a Structurally Constrained Eye Enhancer
Nat. Rev. Urol. doi: /nrurol
The REF-1 Family of bHLH Transcription Factors Pattern C
Suboptimization of developmental enhancers
NsiR4 expression is mediated through an NtcA-activated promoter.
Molecular mechanism of enhanced xylose utilization by XylR mutations.
dex-1 expression in the seam cells is regulated by DAF-16.
Relationship between Genotype and Phenotype
Sequence variation of 16S rRNA gene primer-binding sites.
Molecular structure of MFS1 promoter genotypes.
Nat. Rev. Endocrinol. doi: /nrendo
Inactivation of human TRAC and CD52 genes by TALENs
REV-ERBα deficiency alters the epigenetic landscape and differentially affects clock gene expression in ILC3 subsets. REV-ERBα deficiency alters the epigenetic.
Opening Chromatin Molecular Cell
Presentation transcript:

The trouble with binding sites Joe Pearson 1/11/10

Long-Term Goal: Identify molecular mechanisms regulating midline gene expression Choose midline genes Identify midline CRMs Identify novel motifsIdentify matches to known motifs Test Motifs Confirm upstream regulatorIdentify upstream regulator Incorporate into midline development models

Notch/Su(H) in midline gene regulation Initial sim expression requires Su(H) sim, hlh-m5/8 (mesectoderm), rst F6d (midline) expression is expanded with Notch over-expression Su(H)/Notch required for multiple stages of midline development (Wheeler et al. ’08) Frequent Su(H) binding sites in midline primordium elements ElementSim:TgoSu(H) sim 3.7pE4(5)6 (10) sim 1.0pL21 sim Sandmann30 rho E-Ss21 Tl rst F6d22 ElementSim:TgoSu(H) btl 2330 Sema1b I1F3sC32 hlh m5/814 Kr StH0.610 Kr PP3.032 Sim:Tgo=ACGTG Su(H)=(T/C) (A/G) TG (A/G/T) GAA

Test cases for Sim-Su(H) cooperation rho MLE Sim Su(H) Sim sema1b I1F3sC Sim Su(H) Sim sim1.0pL Sim Su(H) Sim Su(H) Twi

Effects of mutating Sim, Su(H), Twist sites in midline CRMs Sim Required for Sema-1b and sim maintenance Maintains rho expression in midline subset Su(H) Not required for Sema-1b or sim maintenance Required for rho activation, “priming” for Sim maintenance Twist Not required for Sema-1b activation

Problems with Sema-1b results Sim sites required for all expression – including mesectoderm expression at stage 5? Su(H) sites may cause variation of initial expression (difficult to see by  -GFP) – also required for expression in subset of lateral cells Twist sites not required? Morel and Schweisguth, 2000 En Sim Sema-1b:GFP En Sim Sema-1b:GFP

sema-1b I1f3sC gfp expression w.t.SimMutSu(H)MutTwistMut st. 5 st. 9 sema1b I1F3sC Sim Su(H) Sim Su(H) Twi

How I explain sema-1b results Sim – Site #3 may also be Twist site (CACGTG) – Mutation abolishes initial and maintained expression Su(H) – Subtle alteration of levels/expression sharpness? Twist – I didn’t mutate 3 rd Twist site (Sim site #3) CCGCACGTGATT Sim site #3 Twist (for) Twist (rev) BTNP ChIP-Chip, 145 sites * *

CG ’ enhancer cg13333 gfp Motif A: AGGT(A/G)G CAGGTAG TAGGTGG CAGGTAG ACGTG GAGGTAG AAAAS SimTgo: ACGTG GFP Sim En TAGTeam CAGGTAG TAGGTAG CAGGCAG TAGGTAA

CG ’-GFP motif requirements wild-typeMotifA1-4ZldMut13 stage 11 stage 13 stage 14 midline CG ’-GFPSimEn

zelda is required for cg13333 expression Df(1)Exel6253/FM7cTwistGFPDf(1)Exel6253/Df(1)Exel6253 En cg13333 SimTauGFP zld tkr J. Watson

Resolving the CG13333 Cis-Trans conflict zelda is required for CG13333 epidermal and midline expression Zelda sites are not required for CG13333 midline expression How can I resolve zelda-Zelda conflict? – Identify which MotifA site (2,4) sufficient for midline expression – Use S2 cell culture reporter assays/EMSAs to test whether Zelda binds these sites Yes  Zelda is directly regulating CG13333 midline expression No  Zelda is not directly regulating CG13333 midline expression

zelda midline expression J. Watson

CG13333-Zelda