Epigenetic Was Lamarck still right? Was Lamarck still right?

Transcription

Epigenetic Was Lamarck still right? Was Lamarck still right?
Epigenetic
Was Lamarck
still right?
Epigenetik/ v. Eggeling 1
1. Introducing Epigenetics
2. Molecular basis
3. Imprinting
4. Diseases as a model for Epigenetics
5. Methylation and demethylation in development
6. Epigenetic phenomena during cloning and at artificial
fertilization
7. Heritage of environment or acquired traits
- or was Lamarck still right?
Epigenetik/ v. Eggeling 2
1 Introducing Epigenetics
Epigenetik/ v. Eggeling 3
Definition
Epigenetik: (επι [gr]: beneath, over)
In biology, the term epigenetics refers to changes in phenotype (appearance)
or gene expression caused by mechanisms other than changes in the
underlying DNA sequence, hence the name epi- (Greek: over; above) genetics. These changes may remain through cell devision for the remainder
of the cell's life and may also last for multiple generations. However, there
is no change in the underlying DNA sequence of the organism; instead, nongenetic factors cause the organism's genes to behave (or "express
themselves") differently.
Die Epigenetik betrifft Vorgänge, die sich ‘epi’ - d. h. neben oder über der
DNA abspielen und dazu führen, daß die kodierte Information in einem Gen
aktiv wird und einen bestimmten zellulären Prozeß in Gang setzt, der
schließlich zur Ausprägung eines bestimmten Merkmals (Phänotyps) des
Individuums führt
Epigenetik/ v. Eggeling 4
Epigenetic
How epigenetic phenomena were found?
Nucleus transplantation experiments with mice
Egg with only
female nuclei
?
Small placenta
Abortion of fetuses
Egg with only
male nuclei
?
Big placenta
Epigenetik/ v. Eggeling 5
Epigenetic
..but also 3000 years ago epigenetic phenomena were
visible in breeding ....
Maultier (Kreuzung von Eselhengst [donkey] und Pferdestute [mare]): mule
Maulesel (Kreuzung von Pferdehengst [stallion] und Eselstute): hinny
Epigenetik/ v. Eggeling 6
Conclusion
• These results are not compatible with Mendels rules
• There must be factors that lead to differences
depending whether the DNA is processed over
oogenesis or spermatogenesis
Epigenetik/ v. Eggeling 7
Gliederung
2 Molecular bases
Epigenetik/ v. Eggeling 8
Nukleosomen
Nukleosomen bei
der Verpackung
von DNA
Den Kern der
Nukleosomen bilden die
Histone H2A, H2B, H3, H4
(je 2x)
Epigenetik/ v. Eggeling 9
Molecular bases of Epigenetics
• Methylation of so-called CpG-Island
Here one methyl group (CH3) is
added to the cytosine
• Histon deacethylation
• Methylation and histon
deacetylation suppress transcription
• Inactivation by methylation is known
for
Fungi
Plants
Mammals
Epigenetik/ v. Eggeling 10
Molecular bases of Epigenetics
(active)
(inactive)
Interaction with heterochromatin proteins
H3K9 acetylation H3K4 metylation
DNA Methylation
H3K27 methylation
Euchromatin proteins
Epigenetik/ v. Eggeling 11
The cellular memory or the histon code
Nucleosomes with modified tails are
carrier of epigenetic information.
Especially important for the
inheritance of gene expression
Azetyliertes Lysin
Ubiquiniertes Lysin
Methyliertes Lysin
Phosphoryl-Lysin
Methyliertes Arginin
Epigenetik/ v. Eggeling 12
Changing chromatin structure
•
The histon code allow a high number of modification
•
50 Million CpG sites could be methylated or un-methylated
in a haploid genome
•
25000000 combinatorial options for the methylation pattern
•
For this reason the epigenetic variety could very high
Epigenetik/ v. Eggeling 13
The cellular memory or the histon code
Epigenetik/ v. Eggeling 14
3 Imprinting
Epigenetik/ v. Eggeling 15
Imprinting
Definition:
[imprint (engl.): aufdrücken, einprägen]
Genomic imprinting is a genetic phenomenon by which certain genes
are expressed in a parent-of-origin-specific manner. It is an inheritance
process independent of the classical Mendeleian inheritance. Imprinted
genes are either expressed only from the allele inherited from the mother
(eg. H19 or CDKN1C), or in other instances from the allele inherited
from the father (eg. IGF2). Forms of genomic imprinting have been
demonstrated in insects, mammals and flowering plants.
Genomic imprinting is an epigenetic process that involves methylation
and histone modifications in order to achieve monoallelic gene
expression without altering the genetic sequence. These epigenetic marks
are established in the germline and are maintained throughout all somatic
cells of an organism.
Beim Imprinting wird festgelegt, welche Gene von der Mutter oder dem
Vater für eine normale Entwicklung des Kindes ab- bzw. angeschaltet
werden müssen
Epigenetik/ v. Eggeling 16
Imprinting
• Zygotes with only maternal or only paternal genetic
material result not in normal offspring
• Male and female provide an not equal genetic
contribution to offspring
• In men 100 – 200 genes were assumed to be affected by
imprinting (e. g. sex-specific differentially methylated)
Epigenetik/ v. Eggeling 17
Imprinting
GEN A
Mat. Allel
Pat. Allel
GEN B
Mat. Allel
Pat. Allel
Epigenetik/ v. Eggeling 18
Gliederung
4 Diseases as a model for epigenetic
Epigenetik/ v. Eggeling 19
Imprinted chromosomal regions
Epigenetik/ v. Eggeling 20
Diseases as a model for epigenetic
• Uniparental Disomies
• Mutations in the methylation machinery
• Hypo- or hyper methylation in carcinogenesis
Epigenetik/ v. Eggeling 21
Uniparental Disomies (UPD)
Here there is no false imprinting, but
the chromosomes of one single parent
are passed to the offspring.
Microsatellite analysis
But the effect is the same
Zygote
pat
mat
Normal
mat
mat
UPD
Epigenetik/ v. Eggeling 22
Imprinted chromosomal regions
Epigenetik/ v. Eggeling 23
Uniparentale Disomies (UPD)
Angelman-Syndrom (AS) and Prader-Willi-Syndrom (PWS) [15q11-13]
normal situation
PWS
AS
mat
pat
Angelman
Syndrome
PWS
Prader-Willi
syndrome
AS
uniparental Disomy
PWS
AS
pat
mat
pat
mat
active Gene
inactive Gene
Epigenetik/ v. Eggeling 24
Mutations in the methylation machinery
DNA-Cytosin-Methyltransferases
DNMT1
DNMT3a
DNMT3b
Methylation of hemimethylated DNA
new methylation
new methylation
Methyl-CpG-binding proteins
MECP2
Mediate between methylation and
deazetylation
Epigenetik/ v. Eggeling 25
Mutations in the methylation machinery
DNMT1
ATR-X Syndrom
(-thalassaemia, mental retardation,
X-linked)
DNMT3
FMR1
ICF Syndrom
(Immune-deficience, centromeric
instability, facial anomaly)
Fra X Syndrom
(fragile X)
MeCP2
RETT Syndrom
Epigenetik/ v. Eggeling 26
Mutations in the methylation machinery
Rett syndrome – Defect
Methyl binding protein
Binding to methyl groups leads to a deacetylation of local histones and
thereby to suppression of transcription
The Rett syndrome is the most common cause of mental retardation in
women (lethal for male embryos; ca. 1:10000)
Epigenetik/ v. Eggeling 27
Rett syndrome
DNA Methylation
H3K9 acetylation H3K4 metylation
H3K27 methylation
Interaction with heterochromatin proteins
Euchromatin proteins
Epigenetik/ v. Eggeling 28
Beckwith-Wiedemann Syndrom
(BWS)
maternal
paternal
active
inactive
chromatin disruption
Epigenetik/ v. Eggeling 29
Cancer and methylation
Inactivation of the tumor suppressor gene p16 by methylation
Promotor
exon 1
CpG islands
exon 2
exon 3
RNA
Tumor suppressor (Protein)
M M M
M M M
exon 1
exon 2
exon 3
no suppressor
Further proliferation of maligne cells
Epigenetik/ v. Eggeling 30
Epigenetik/ v. Eggeling 31
Cancer and methylation
• Global hypo-methylation, but local hyper-methylation
• Silencing of TSGs leads to growth advantage (methylation
of pRB leads to unilateral Retinoblastoma, of VHL renal
cell carcinoma)
• Silencing of mismatch repair genes (MMR) stops repair ->
accumulation of mutation
• Elevated methylation with age
• 5-Methylcytosine could chemically affected easily ->
mutations (e.g. Melanoma: meth-C -> UV -> T)
Epigenetik/ v. Eggeling 32
Methylation and aging
Epigenetik/ v. Eggeling 33
Summary (Imprinting and diseases)
• For the proper development of offspring the
appropriate genes has to be imprinted
• So, for one gene the maternal allele has to be
inactivated, but the paternal activated. For another
gene it could be vice versa
• False imprinting pattern, but also defects or loss of
enzymes, which act methylation, result in several
diseases
Epigenetik/ v. Eggeling 34
Gliederung
5 Methylation und Demethylation
during Development
Epigenetik/ v. Eggeling 35
Methylation und Demethylation during Development
Epigenetik/ v. Eggeling 36
Methylation und Demethylation during Development
Generationswechsel
imprinted methylated genes
imprintete non-methylated genes
non-imprinted maternal genes
non-imprinted paternal genes
Epigenetik/ v. Eggeling 37
Detection of Methylation
Immuno staining of a mouse zygote with Anti-5-Methylcytosin
paternal
3h
6h
8h
maternal
2 cell-state
22h
32h
4 cell-state
45h
Meyer et al. 2000
Epigenetik/ v. Eggeling 38
Where epigenetic modifications can be set?
Deletion of
methylation of not
imprinted genes
Fertilization
Embryo
Environmental
impacts
Adult
Germ cells
Deletion of all
methylation
Cloning and in-vitro Fertilization (IVF) can lead to problems!
Epigenetik/ v. Eggeling 39
Epigenetik/ v. Eggeling 40
Summary (Methylation and Development)
• Methylation or imprints will be deleted in
primordial germ cells and in zygote completely or
partially, respectively
• How acquired characteristics or influences from
development can be inherited?
Epigenetik/ v. Eggeling 41
6 Epigenetic phenomena during cloning and invitro fertilization
Epigenetik/ v. Eggeling 42
Epigenetic und Cloning
Somatic cell
Enucleated egg
Genome of only one single parent!
Clone
Epigenetik/ v. Eggeling 43
Epigenetic und Cloning
The cloned lamb is bigger and dies earlier!
Epigenetik/ v. Eggeling 44
Epigenetic und in-vitro fertilization (IVF)
Also by in-vitro fertilization and especially by ICSI (intra
cytoplasmatic Sperm injection) there are data indicating on
problems:
 Children are smaller
 The probability by ICSI is higher for BeckwithWiedemann Syndrome (11p15)
 Children get more often a Retinoblastom
Epigenetik/ v. Eggeling 45
7 Heritage of environmental influences or
acquired traits
- was Lamarck still right?
Epigenetik/ v. Eggeling 46
Heritage of environmental influences or acquired traits
Drosophila (fruit fly)
Special elements (Fab-7) can be inherited epigenetically
through mitosis and meiosis
(Cavalli und Paro 1998; Cell)
Epigenetik/ v. Eggeling 47
Heritage of environmental influences or acquired traits
Mouse:
Special nutrition
Fur color stays
changed over
generations
Treatment with
cancerogenic
drugs
Also offspring
have a higher
incidence for
tumors
Malnutrition
Offspring are
smaller
Epigenetik/ v. Eggeling 48
Heritage of environmental influences or acquired traits
Human:
Father have had
a low intake in his
SGP
Lower lethality from
cardiovascular
diseases
Generally reach
higher age
Grandfather
has eaten a lot
Macrodome of mother
by malnutrition
during early
embryonic
development
High lethality
from diabetes
Children with lower weight and
height
Epigenetik/ v. Eggeling 49
Darwin und Mendel
Darwin postulated selection as main
mechanism in evolution
Charles Darwin (1809-1882)
Mendel proved that traits can be inherited in
a special way
Gregor Mendel (1822-1884)
Epigenetik/ v. Eggeling 50
Was war Lamarcks Theorie?
Quintessence of Lamarckism
 Animal adapt to a changing environment. The acquired traits
are inherited, if both parents possess them
Jean-Baptiste Lamarck
(1744-1829)
• Introduced the term
„Biology“
• Introduced the term of
animal classes
Epigenetik/ v. Eggeling 51
Lamarcks therory as als ideology
Trofim Lyssenko (1898-1976) -> Lyssenkoism
• Aquired traits could be inherited
• Species can be convertedt o each other
He is responsible for the shameful backwardness of Soviet biology
and of genetics in particular, for the dissemination of pseudoscientific views, for adventurism, for the degradation of learning,
and for the defamation, firing, arrest, even death, of many genuine
scientists (1964).
Epigenetik/ v. Eggeling 52
Georg Schneider (1909-1970)
Director of the Ernst-Haeckel-House. Brought theories of
Lyssenkos to Jena
Epigenetik/ v. Eggeling 53
Bisherige Kritik an Lamarcks Theorie
Criticism to Lamarck's evolution theory:
Lamarcks evolution theory has a big error,
because it tells that individually aquired traits
will be inherited; that means that genetic
information has to be changed in the germ
cells.
Epigenetik/ v. Eggeling 54
Epigenetik/ v. Eggeling 55
Facts to caesarean section;
•In Brasilia 4 of 5 women
•In USA 4 of 10
•In Germany 3 of 10
Allergy
Astma
Diabetes Typ 1
20 % higher methylation of lymphocytes
Is birth may be to fast?
Epigenetik/ v. Eggeling 56
Fearless by methylation antagonists?
• Suizid patients – special genes in brain are higher methylated
• Children misused have lower activity of glucocortikoid
receptor
• Rats with deficits in parental care have a lower stress tolerance
Epigenetik/ v. Eggeling 57
Some additional Facts:
Epigenetik/ v. Eggeling 58
70% of the human genome are
transcribed - but only 2% encode
for proteins! | © dkfz.de
Epigenetik/ v. Eggeling 59
Short and long noncoding RNA
Coding or
functional
RNA
(fRNA)
Noncoding
RNA
(ncRNA)
Small
nucleolar
(snoRNA)
Transfer
RNA (tRNA)
Ribosomale
RNA (rRNA)
microRNA
(miRNA)
Short/small
interferring
(siRNA)
Long
noncoding
(lncRNA)
Piwiinteracting
(piRNA)
Piwi: P-element induced wimpy testis (Drosophila)
Epigenetik/ v. Eggeling 60
Long non-coding RNAs (long ncRNAs, lncRNA)
are in general considered (somewhat arbitrarily) as
non-protein coding transcripts longer than 200
nucleotides.
A recent study found only one-fifth of transcription
across the human genome is associated with
protein-coding genes, indicating at least four-times
more long non-coding than coding RNA sequences.
But lncRNA could also code for proteins!
Epigenetik/ v. Eggeling 61
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Epigenetik/ v. Eggeling 63
2011
Epigenetik/ v. Eggeling 64
Conclusion:
• Epigenetic is an additional way of
inheritance
• Investigation in men and mice could show
that influences of environment can be
transmitted to the next generation
• The molecular mechanisms stay unclear
until now
• The evolutionary advantage of epigenetic
could be a faster adaption to a changing
environment
Epigenetik/ v. Eggeling 65
What is coming up?
Epigenetik/ v. Eggeling 66
Zusätzliche Folien
Epigenetik/ v. Eggeling 67
Hatte jetzt Lamarck doch recht?
JA und NEIN
 Epigenetik ist ein zusätzliche Form der Vererbung
 Umwelteinflüsse können über Generationen
weitergegeben werden.
 Können dies aber erworbene Eigenschaften sein?
 Molekulare Mechnismen, die eine epigenetische
Vererbung über Generationen ermöglichen sind bisher
nur ansatzweise erkannt
Epigenetik/ v. Eggeling 68
Durch wissenschaftliche Forschungen hat das
anthropozentrische Weltbild viele Kränkungen erfahren
Kopernikus
Darwin
Human Genom Projekt
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Methylierung und Demethylierung
Epigenetik/ v. Eggeling 78
Molekulare Grundlagen der Epigenetik
Methylierung
Nachteile
• Erhöhung der Mutationsrate
(5-Methylcytosine als
endogenes Mutagen)
• Wichtige Gene, die die
Proliferation steuern, können
inaktiviert werden (z. B. TSG,
MMR)
• Änderung der Stabilität der
Chromatinstruktur
• Homologe Rekombination ist
reduziert
Vorteile
• X-Chromosome
Inaktivierung
• Suppression von
parasitären Sequenzen
• Imprinting
Epigenetik/ v. Eggeling 79
Begriffsdefinition
Genetik
Epigenetik
wie können Umwelteinflüsse
zu Mutationen in den Genen
führen?
Können Umwelteinflüsse den
regulatorischen Zustand der
Gene verändern?
Epigenetik/ v. Eggeling 80
Molecular bases of Epigenetics
common disease genetic and epigenetic (CDGE)
Epigenetik/ v. Eggeling 81
Jean Baptiste Lamarck
Rudyard Kipling
„adaptive change“
Epigenetik/ v. Eggeling 82