Prezentacja programu PowerPointbiotka.mol.uj.edu.pl/zbm/handouts/2005_01_receptors.pdf · HIF-1,...

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Nuclear receptors Nuclear receptors structure structure and function and function

Transcript of Prezentacja programu PowerPointbiotka.mol.uj.edu.pl/zbm/handouts/2005_01_receptors.pdf · HIF-1,...

Page 1: Prezentacja programu PowerPointbiotka.mol.uj.edu.pl/zbm/handouts/2005_01_receptors.pdf · HIF-1, NR, NR, NR NR, NR, NR. Power of. nuclear. receptors….. Prof. Laura Kufman Uniwerytet

Nuclear receptorsNuclear receptors

structure structure and functionand function

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NRNR

NRNR

NRNR

NRNR

NRNR

NRNR

NRNR

NRNR

NRNR

NRNR

NRNR

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Let’s start from a small fragment..... (?)Let’s start from a small fragment..... (?)

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Types of Types of leukemiasleukemias

A.A.

-- LymphoLymphoidid

-- MyeloMyeloidid

B.B.

-- acuteacute(results from a transformation relatively undifferentiated proge(results from a transformation relatively undifferentiated progenitor cells, with only limited nitor cells, with only limited capabilities of differentiation)capabilities of differentiation)

-- chronicchronic(results from a transformation of more differentiated cells, whi(results from a transformation of more differentiated cells, which have capability to mature)ch have capability to mature)

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Chronic Chronic myelomyeloidid leukemia (CML)leukemia (CML)-- sustains about sustains about 3% of cancers3% of cancers in humans (15in humans (15--20% all 20% all leukemiasleukemias in adults), in adults), approximately approximately 11--2 cases per 100 000 people2 cases per 100 000 people

-- average ageaverage age of diagnosed patients: of diagnosed patients: 53 years53 years (30% patients is older than 60 years, (30% patients is older than 60 years, less than 10% less than 10% underunder 20 years20 years ofof ageage))

-- in about half of patients the disease is in about half of patients the disease is asympthomaticasympthomatic and is detected during and is detected during routine blood controlroutine blood control

-- untreated is fataluntreated is fatal

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Chronic Chronic myelomyeloidid leukemia (CML)leukemia (CML)-- First cancer for which the First cancer for which the geneticalgenetical mutation causing the disease has been identified mutation causing the disease has been identified (1960, Philadelphia)(1960, Philadelphia)

-- Mutated chromosome Philadelphia forms after translocation fragmMutated chromosome Philadelphia forms after translocation fragment of long arm of ent of long arm of chromosome 9 (coding chromosome 9 (coding AblAbl kinasekinase) to long arm ) to long arm of chromosome 22 (coding of chromosome 22 (coding BcrBcr....) ....) (9 22)(9 22)

-- This mutation is present in 95% patients with This mutation is present in 95% patients with CML; it can also be found in CML; it can also be found in patintspatints with other with other leukemiasleukemias (e.g. in 15(e.g. in 15--30% cases of acute 30% cases of acute lymphoid leukemia)lymphoid leukemia)

-- Translocation leads to formation of hybrid geneTranslocation leads to formation of hybrid geneBcr/AblBcr/Abl and fusion protein of constitutive, and fusion protein of constitutive, unregulated unregulated kinasekinase activityactivity

Chromosome 9 Chromosome 9’

Chromosome 22 Philadelphia

AblBcr

Bcr/Abl

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TranslocationTranslocationBCRBCR--AblAbl

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Diagnostics of CMLDiagnostics of CML

-- in vast majority of patients Philadelphiain vast majority of patients Philadelphiachromosome can be detected using the chromosome can be detected using the StandarStandar cytogeneticcytogenetic methodsmethods

-- other good tools are FISH or RTother good tools are FISH or RT--PCRPCR

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Normal Normal AblAbl tyrosine tyrosine kinasekinase in leukocytes is associated with regulation of cell proliferatioin leukocytes is associated with regulation of cell proliferation n and differentiationand differentiation

BcrBcr--AblAbl kinasekinase, which is constitutively active leads to:, which is constitutively active leads to:-- increased proliferationincreased proliferation-- decreased rate of apoptosisdecreased rate of apoptosis-- decreased expression of decreased expression of adhesinsadhesins (attenuation of adhesion and disturbed signal (attenuation of adhesion and disturbed signal transduction from a bone morrow transduction from a bone morrow microenviromentmicroenviroment))

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Chronic Chronic myelomyeloidid leukemia (CML)leukemia (CML)- The most common symptoms at presentation in the chronic phase of CML include:fatigue, weight loss, abdominal fullness, bleeding, and sweating.

- As the disease progresses, bone pain and pain from splenic infarction may be seen, and end stage CML may present with signs and symptoms of acute leukaemia.

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Chronic Chronic myelomyeloidid leukemialeukemia(CML)(CML)Therapy:Therapy:

-- Bone mBone moorrowrrow transplantation transplantation (achievable for (achievable for less than 20% of new diagnosed patients)less than 20% of new diagnosed patients)

-- Treatment with interferonTreatment with interferon--α (α (IFNIFNαα))

-- chemotherapychemotherapy (e.g. (e.g. hydroxyureahydroxyurea))

-- GlGlivivecec

At advanced phase no treatment is effectiveAt advanced phase no treatment is effective

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GlGliivecvec ((imatinibimatinib))

-- first commercially available inhibitorfirst commercially available inhibitorof tyrosine of tyrosine kinasekinase accepted for a accepted for a clinical useclinical use

-- specifically inhibits specifically inhibits kinaseskinases BcrBcr--AblAbl, c, c--Kit (CD117) and PDGFKit (CD117) and PDGF--RR

-- this way it inhibits proliferation and apoptosis of cells exprethis way it inhibits proliferation and apoptosis of cells expressing those ssing those kinaseskinases

-- causes relatively mild sidecauses relatively mild side--effecteffect

-- significant improvement is observed in 49% significant improvement is observed in 49% pacjentówpacjentów in the chronic phase of CML, in the chronic phase of CML, who did not respond to treatment with who did not respond to treatment with IFNIFNαα

glivec

22--phenylaminopyrimidine derivativephenylaminopyrimidine derivative

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KinaKinasesses inhibitedinhibited byby glgliivecvec

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II II phasephase clinicalclinical trialtrial withwith glgliivecvec

532 532 patientspatients, 1, 1-- > 5 > 5 yearsyears ofof diagnosisdiagnosis, 400 mg , 400 mg glivecglivec//dayday

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HIFHIF--11

, NR

, NR

, NR

NR

, NR

, NR

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Power Power ofof nuclearnuclear receptorsreceptors…..…..

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Prof. Laura Prof. Laura KufmanKufmanUniwerytetUniwerytet JagiellońskiJagielloński

19171917

AmbystomaAmbystoma mexicanummexicanum

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-- -- Nuclear receptors exist in the all Nuclear receptors exist in the all MetazoaMetazoa sstudiedtudied, , but have not been found in the other organismsbut have not been found in the other organisms

-- Most of receptors are very old and conservative: mammalian protMost of receptors are very old and conservative: mammalian proteins eins have their counterparts in insectshave their counterparts in insects

-- NNuclear receptors sustain of one uclear receptors sustain of one superfamilysuperfamily, originating perhaps from , originating perhaps from one ancestorone ancestor

-- Primary nuclear receptor acted possibly as a constitutive, Primary nuclear receptor acted possibly as a constitutive, homodimerichomodimerictranscription factortranscription factor

Evolution of nuclear receptorsEvolution of nuclear receptors

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--inin CCenorhabditisenorhabditis eleganselegans more than 200more than 200 different different nucleanuclear r receptors have been found, receptors have been found, but in Drosophila but in Drosophila melanogastermelanogaster only 21 (they mediates e.g. action of only 21 (they mediates e.g. action of ekdysomeekdysome))

-- in human there are in human there are 4848 nuclear receptor genesnuclear receptor genes

-- on the protein level the number of receptors is higher on the protein level the number of receptors is higher ((alternative alternative splicing,splicing, different promoters,different promoters,postranslationalpostranslational modificationsmodifications))

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Modular structure of nuclear receptorsModular structure of nuclear receptors

A typical nuclear receptor is composed of A typical nuclear receptor is composed of several domains The variable NH2The variable NH2--terminal region (terminal region (region region

A/BA/B) contains the ) contains the ligandligand--independent independent AFAF--11transactivationtransactivation domain.domain.

The conserved DNAThe conserved DNA--binding domain binding domain ((DBD, region CDBD, region C) is responsible for the ) is responsible for the recognition of specific DNA sequencesrecognition of specific DNA sequences

A variable linker A variable linker region Dregion D connects DBD connects DBD to the E/F regionto the E/F region

The conserved The conserved E/FE/F region contains region contains ligandligandbinding domain (binding domain (LBDLBD), ), dimerizationdimerizationstructure and structure and ligandligand--dependenddependend AF2 AF2 transactivationtransactivation domain

several domains

domain

ArandaAranda A. & A. & PascualPascual A. A. PhysiolPhysiol Rev 2001.Rev 2001.

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RRegion A/Begion A/B

The most variable in respect of size and sequence. Very often iThe most variable in respect of size and sequence. Very often it includes AFt includes AF--1. 1.

The alternative splicing occurs usually within this domainThe alternative splicing occurs usually within this domain

Perhaps this domain is responsible for cellPerhaps this domain is responsible for cell--specific action of the nuclear receptorsspecific action of the nuclear receptors

It can be It can be phosphorylatedphosphorylated by different by different kinaseskinases involved in signal transduction involved in signal transduction (MAPK, (MAPK, cyclinecycline--dependent dependent kinaseskinases)), which regulates the activity of the receptor, which regulates the activity of the receptor

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RRegion DBDegion DBD (domain C)(domain C)

The most conservative domain responsible for recognizing of theThe most conservative domain responsible for recognizing of the consensesconsenses sequences of sequences of DNADNA

There are There are 2 2 zinc fingers divided by the fragment of zinc fingers divided by the fragment of 6060--70 70 aminoacidsaminoacids –– in each finger in each finger four four cysteinescysteines coordinates one zinc ioncoordinates one zinc ion

The sequence at the base of the first finger The sequence at the base of the first finger (P box) (P box) recognizes DNA, whereas the recognizes DNA, whereas the sequence at the base of the second finger sequence at the base of the second finger (D box) (D box) is involved in the receptor is involved in the receptor dimerizationdimerization

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DBD of nuclear receptorDBD of nuclear receptor DBDDBD consists of two zinc fingers. In the zinc consists of two zinc fingers. In the zinc fingers, four conserved fingers, four conserved cysteinescysteines coordinate a coordinate a zinc ion.zinc ion.

First finger contains First finger contains P boxP box residues, involved residues, involved in the discrimination of the response elementin the discrimination of the response element

Second finger contains Second finger contains D boxD box, which form a , which form a dimerizationdimerization interfaceinterface

CTE CTE (COOH(COOH--terminal extension) is critical for terminal extension) is critical for monomericmonomeric DNA bindingDNA binding

ArandaAranda A. & A. & PascualPascual A. A. PhysiolPhysiol Rev 2001.Rev 2001.

Fingers form the DBDFingers form the DBDthat recognizes a hemithat recognizes a hemi--sitesiteof the response elementof the response element

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HingHingee rregion egion (domain D)(domain D)

Moderately conservative,Moderately conservative, bindsbinds DBD DBD andand LBD, LBD, allowingallowing for a for a rotationrotation ofof DBDDBD

VeryVery oftenoften itit includesincludes a a nuclearnuclear localizationlocalization signalssignals

MutationsMutations withinwithin thisthis region region unablesunables thethe interactioninteraction ofof thethe receptor receptor withwith coco--repressorsrepressors

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RRegion LBDegion LBD ((domaindomain E)E)ItIt bindsbinds ligand ligand andand mediatesmediates homohomo-- oror heterohetero--dimerdimerizationization andand interationinteration withwith heatheat

shockshock proteinsproteins

On On thethe 1212thth helisehelise itit containscontains anan AFAF--22 domaindomain, , responsibleresponsible for a ligandfor a ligand--dependent dependent transactivationtransactivation. . MutationsMutations withinwithin AF2 AF2 maymay leadlead to e.g. to e.g. androgenandrogen--insensitivityinsensitivity syndromesyndrome, , oror thyroidthyroid hormoneshormones--insensitivityinsensitivity syndomesyndome..

ThisThis domaindomain incluesinclues alsoalso otherother sequencessequences necessarynecessary for for transactivationtransactivation disperseddispersed inin thetherestingresting receptor, but receptor, but locatedlocated closelyclosely eacheach otherother uponupon ligand ligand bindingbinding..

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Unligated Ligated

LBD of nuclear receptorLBD of nuclear receptor

Cylinders represents aCylinders represents a--helices that are helices that are numbered from 1numbered from 1--12.12.

Note different position of the COOHNote different position of the COOH--terminal helix 12 that contains the core terminal helix 12 that contains the core AFAF--2 domain2 domain

ArandaAranda A. & A. & PascualPascual A. A. PhysiolPhysiol Rev 2001.Rev 2001.

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Domain structure of nuclear receptorsDomain structure of nuclear receptors

A. LazarA. Lazar

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N-terminal DBD LBD

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NNuclearuclear receptorsreceptors regulateregulate transcriptiontranscription throughthrough bindingbinding to consensus to consensus sequencesequence inin thethe targettarget genesgenes. . TheseThese sequencessequences areare usuallyusually locatedlocated withinwithinpromoterpromoter, but , but sometimessometimes theythey areare eveneven severalseveral thousandthousand nucleotidesnucleotides upup--oror downdown--streamstream ofof thethe start start ofof transcriptiontranscription sitesite..

TATA box

TATA box

TATA box

TATA box

consensus consensus sequensesequense

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Signal transduction by Signal transduction by hormonshormons via nuclear receptvia nuclear recept

A. LazarA. Lazar

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Consensus Consensus sequencessequences ofof nuclearnuclear receptorsreceptors

Consensus Consensus sequencesequence consistsconsists ofof 6 6 nunucleotidescleotides: :

AGAGAAAACACA ((recognizedrecognized by by thethe steroid steroid hormonehormone receptorsreceptors))

AGAGGGTCATCA ((recognizedrecognized by by thethe otherother receptorsreceptors))

AGAGTTTCATCA ((recognizedrecognized by by thethe otherother receptorsreceptors))

fragment fragment ofofacylCoAacylCoA oxidaseoxidasepromoterpromoter

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SomeSome nuclearnuclear receptorsreceptors actact as as monomermonomerssbindingbinding to to hexamerhexamer ofof nucleotidesnucleotides..

Most Most receptorsreceptors actact as as dimersdimers, , bindingbinding to to thethe sequencesequence ofof twotwo hexamershexamers

DimersDimers cancan be be bothboth homohomo-- oror heterodimersheterodimers. In . In thethe latterlatter casecase thethe partner for partner for heterodimerizationheterodimerization isis alwaysalways a a nuclearnuclear receptor receptor RXR

e.g.e.g. NurrNurr--11

RXR

RXRRXRERERGR

RARRARTRTRVDRVDRPPAR

GR

PPAR

homodimershomodimers heterodimersheterodimers

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Consensus Consensus sequencessequences ofof nuclearnuclear receptorsreceptors

consensus consensus sequencessequences recognizedrecognized by a by a dimersdimers cancan be:be:

palindrompalindromss ((onlyonly suchsuch sequencessequences cancan be be recognizedrecognized by steroid by steroid hormonehormone receptorsreceptors))

reversedreversed palindromspalindroms

directdirect repetitionsrepetitions (DR1, DR2, DR3 etc.)

AGGTCA...TGACCTAGGTCA...TGACCTTCCAGT...ACTGGATCCAGT...ACTGGA

ACTGGA...TCCAGTACTGGA...TCCAGTTGACCT...AGGTCATGACCT...AGGTCA

(DR1, DR2, DR3 etc.)

AGGTCA...AGGTCAAGGTCA...AGGTCATCCAGT...TCCAGTTCCAGT...TCCAGT

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Binding of receptors toBinding of receptors to theirtheir consensus consensus sequencessequences

Receptors can bind as monomers, Receptors can bind as monomers, homodimershomodimers or RXR or RXR heterodimersheterodimers..

Steroid receptors bind as Steroid receptors bind as homodimershomodimers to to palindromicpalindromicelements spaced by three elements spaced by three nucleotides.nucleotides.

MonomericMonomeric binding requires the binding requires the halfhalf--core motif precede by a 5’core motif precede by a 5’--flanking A/T reach sequence.flanking A/T reach sequence.

HeterodimersHeterodimers can can recognmizerecognmizediverse diverse HREsHREs in which halfin which half--core core motifs can be arranged as motifs can be arranged as polindromespolindromes, direct repeats or , direct repeats or inverted inverted polindromespolindromes

ArandaAranda A. & A. & PascualPascual A. A. PhysiolPhysiol Rev 2001.Rev 2001.

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Permissive and nonPermissive and non--permissive permissive heterodimerheterodimer

Permissive Permissive heterodimersheterodimers, such as PPAR/RXR, can be activated by , such as PPAR/RXR, can be activated by ligandsligandsof either RXR or its partner receptor and are synergistically acof either RXR or its partner receptor and are synergistically activated in the tivated in the presence of both presence of both ligandsligands..

ArandaAranda A. & A. & PascualPascual A. A. PhysiolPhysiol Rev 2001.Rev 2001.

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Permissive and nonPermissive and non--permissive permissive heterodimerheterodimer

In In nonnon--permissive permissive heterodimersheterodimers, such as RXR/RAR, , such as RXR/RAR, heterodimerizationheterodimerizationprecludes binding of the RXR precludes binding of the RXR ligandligand. .

Binding of Binding of ligandligand to the RAR moiety causes receptor activation and allows to the RAR moiety causes receptor activation and allows binding of the RXR binding of the RXR ligandligand resulting in synergism. resulting in synergism.

ArandaAranda A. & A. & PascualPascual A. A. PhysiolPhysiol Rev 2001.Rev 2001.

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Mechanism of action of nuclear receptorsMechanism of action of nuclear receptors

LigandLigand can be generated in three different can be generated in three different ways: ways:

11) an active ) an active ligandligand or hormone is synthesized in a or hormone is synthesized in a classical endocrine organ and enters the cell, classical endocrine organ and enters the cell,

22) the ) the ligandligand may be generated from a precursor or may be generated from a precursor or prohormoneprohormone within the target cell, and within the target cell, and

33) the ) the ligandligand may be a metabolite synthesized may be a metabolite synthesized within the target cell.within the target cell.

The The unligandedunliganded receptor may have a nuclear receptor may have a nuclear location. However, some steroid receptors are location. However, some steroid receptors are cytoplasmiccytoplasmic in the absence of in the absence of ligandligand due to their due to their association with a large association with a large multiproteinmultiprotein complex of complex of chaperones, including Hsp90 and Hsp56. chaperones, including Hsp90 and Hsp56. LigandLigandbinding induces dissociation of the complex and binding induces dissociation of the complex and nuclear translocation. Once in the nucleus, the nuclear translocation. Once in the nucleus, the receptors regulate transcription by binding, receptors regulate transcription by binding, generally as generally as dimersdimers, to hormone response , to hormone response elements (elements (HREsHREs) normally located in regulatory ) normally located in regulatory regions of target genes.

Nuclear receptors are Nuclear receptors are activated after activated after ligandligand binding. binding.

ArandaAranda A. & A. & PascualPascual A. A. PhysiolPhysiol Rev 2001.Rev 2001.

regions of target genes.

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ClassificationClassification ofof nuclearnuclear receptorsreceptors-- on on thethe basisbasis ofof primaryprimary structurestructure nuclearnuclear receptorsreceptors theythey cancan be be classifiedclassified to to 7 7 familiesfamilies, , but one but one familyfamily maymay containcontain receptorsreceptors for for veryvery distinctdistinct ligandsligands, , whereaswhereas thethe same ligand same ligand cancan be be boudboud by by membersmembers ofof differentdifferent familiesfamilies..

On On thethe basisbasis ofof ligand ligand bindingbinding andand dimerizationdimerization nuclearnuclearreceptorsreceptors cancan be be classifiedclassified to to 4 4 typtypeses::

TypTypee II ((homodimerhomodimericic receptorreceptorss ofof steroid steroid hormoneshormones)) –– e.g.e.g. ER,ER, AR, GR, MR.AR, GR, MR.

TypTypee IIII ((hodimerichodimeric orphansorphans) ) –– e.g. e.g. RXRRXR

TTypypee IIIIII ((heterodimersheterodimers) ) –– e.g. e.g. TRTR, , RAR, VDR, PPAR.RAR, VDR, PPAR.

TypTypee IVIV ((monomericmonomeric orphansorphans) ) –– e.g. Nurre.g. Nurr--11

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Mechanism of action of nuclear receptorsMechanism of action of nuclear receptors

Nuclear receptors can be also Nuclear receptors can be also activated independently of activated independently of ligandligandbinding. binding.

Some receptors may be Some receptors may be constitutively active. constitutively active.

Activity of others is modulated by Activity of others is modulated by other means, for instance other means, for instance phosphoryphosphory--lationlation mediated by mediated by hormones and growth factors that hormones and growth factors that stimulate diverse signal stimulate diverse signal transduction pathways.transduction pathways.

ArandaAranda A. & A. & PascualPascual A. A. PhysiolPhysiol Rev 2001.Rev 2001.

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ThankThank youyou andand seesee youyou nextnext weekweek......

WhatWhat wouldwould be be profitableprofitable to to rememberremember inin JuneJune::

-- structurestructure ofof nuclearnuclear receptorsreceptors

-- thethe wayway ofof actionaction ofof nuclearnuclear receptorsreceptors

SSlideslides cancan be be foundfound inin thethe librarylibrary andand atat thethe HemeHeme OxygenaseOxygenase Fan Fan ClubClubpagepage::

https://https://biotka.mol.uj.edu.pl/~hemeoxygenasebiotka.mol.uj.edu.pl/~hemeoxygenase