Docstoc

Epigenetic

Document Sample
Epigenetic Powered By Docstoc
					From Wikipedia, the free encyclopedia

Epigenetics

Epigenetics
become fully differentiated cells. In other words, a single fertilized egg cell - the zygote - changes into the many cell types including neurons, muscle cells, epithelium, blood vessels et cetera as it continues to divide. It does so by activating some genes while inhibiting others. [3]

This article is part of the series on: Gene expression a Molecular biology topic (portal) (Glossary) Introduction to Genetics General flow: DNA > RNA > Protein special transfers (RNA > RNA, RNA > DNA, Protein > Protein) Genetic code Transcription Transcription (Transcription factors, RNA Polymerase,promoter) post-transcriptional modification (hnRNA,Splicing) Translation Translation (Ribosome,tRNA) post-translational modification (functional groups, peptides, structural changes) gene regulation epigenetic regulation (Hox genes, Genomic imprinting) transcriptional regulation post-transcriptional regulation (sequestration, alternative splicing,miRNA) post-translational regulation (reversible,irrevesible) 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 divisions 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;[1] instead, non-genetic factors cause the organism’s genes to behave (or "express themselves") differently.[2] The best example of epigenetic changes in eukaryotic biology is the process of cellular differentiation. During morphogenesis, totipotent stem cells become the various pluripotent cell lines of the embryo which in turn

Etymology and definitions
According to Dr. Steve Folmar, the word epigenetics has had many definitions, and much of the confusion surrounding its usage relates to these definitions having changed over time. Initially it was used in a broader, less specific sense but it has become more narrowly linked to specific molecular phenomena occurring in organisms.[4] Epigenetics (as in "epigenetic landscape") was coined by C. H. Waddington in 1942 as a portmanteau of the words genetics and epigenesis.[5] Epigenesis (see contrasting principle of preformationism) is an older word to describe the differentiation of cells from their initial totipotent state in embryonic development. When Waddington coined the term the physical nature of genes and their role in heredity was not known; he used it as a conceptual model of how genes might interact with their surroundings to produce a phenotype. Robin Holliday defined epigenetics as "the study of the mechanisms of temporal and spatial control of gene activity during the development of complex organisms."[6] Thus epigenetic can be used to describe any aspect other than DNA sequence that influences the development of an organism. The modern usage of the word is more narrow, referring to heritable traits (over rounds of cell division and sometimes transgenerationally) that do not involve changes to the underlying DNA sequence.[7] The Greek prefix epi- in epigenetics implies features that are "on top of" or "in addition to" genetics; thus epigenetic traits exist on top of or in addition to the traditional molecular basis for inheritance. The similarity of the word to "genetics" has generated many parallel usages. The "epigenome" is a parallel to the word "genome," and refers to the overall epigenetic state of a cell. The phrase "genetic code" has also been adapted—the "epigenetic code" has been used to describe the set of epigenetic features that create different phenotypes in different cells. Taken to its extreme, the "epigenetic code" could represent the total state of the cell, with the position of each molecule accounted for; more typically, the term is used in reference to systematic efforts to measure specific, relevant forms of

1

From Wikipedia, the free encyclopedia
epigenetic information such as the histone code or DNA methylation patterns. Epigenetic was also used by the psychologist Erik Erikson in his Psychosocial development theory, however that usage is of primarily historical interest. [8]

Epigenetics

Molecular basis of epigenetics
The molecular basis of epigenetics is complex. It involves modifications of the activation of certain genes, but not the basic structure of DNA. Additionally, the chromatin proteins associated with DNA may be activated or silenced. This accounts for why the differentiated cells in a multi-cellular organism express only the genes that are necessary for their own activity. Epigenetic changes are preserved when cells divide. Most epigenetic changes only occur within the course of one individual organism’s lifetime, but some epigenetic changes are inherited from one generation to the next.[9] Specific epigenetic processes include paramutation, bookmarking, imprinting, gene silencing, X chromosome inactivation, position effect, reprogramming, transvection, maternal effects, the progress of carcinogenesis, many effects of teratogens, regulation of histone modifications and heterochromatin, and technical limitations affecting parthenogenesis and cloning. Epigenetic research uses a wide range of molecular biologic techniques to further our understanding of epigenetic phenomena, including chromatin immunoprecipitation (together with its large-scale variants ChIP-on-chip and ChIP-seq), fluorescent in situ hybridization, methylation-sensitive restriction enzymes, DNA adenine methyltransferase identification (DamID) and bisulfite sequencing. Furthermore, the use of bioinformatic methods is playing an increasing role (computational epigenetics).

DNA associates with histone proteins to form chromatin. remodeling is accomplished through several distincly different mechanisms: 1. The first way is post translational modification of the amino acids that make up histone proteins. Histone proteins are made up of long chains of amino acids. If the amino acids that are in the chain are changed, the shape of the histone sphere might be modified. DNA is not completely unwound during replication. It is possible, then, that the modified histones may be carried into each new copy of the DNA. Once there, these histones may act as templates, initiating the surrounding new histones to be shaped in the new manner. By altering the shape of the histones around it, these modified histones would ensure that a differentiated cell would stay differentiated, and not convert back into being a stem cell. 2. The second way is the addition of methyl groups to the DNA, at CpG sites, to convert cytosine to 5-methylcytosine. Cytosine is the nucleotide that our cells can "read." Our cells cannot "read" methylcytosine. If DNA is conceived as an instruction manual again, changing cytosine to methylcytosine would be like changing the font on a Word document to "wingdings." The contention would be that since the cell can no longer "read" the gene, the gene is turned off. The way that the cells stay differentiated in the case of DNA methylation is clearer to us than it is in the case of histone shape. Basically, certain enzymes (such as DNMT1) have a higher affinity for the methylated cytosine. If this enzyme reaches a "hemimethylated" portion of DNA (where methylcytosine is in only one of the two DNA strands) the enzyme will methylate the other half.

Mechanisms
Several types of epigenetic inheritance systems may play a role in what has become known as cell memory:[10]

DNA methylation and chromatin remodeling
Because the phenotype of a cell or individual is affected by which of its genes are transcribed, heritable transcription states can give rise to epigenetic effects. There are several layers of regulation of gene expression. One way that genes are regulated is through the remodeling of chromatin. Chromatin is the complex of DNA and the histone proteins with which it associates. Histone proteins are little spheres that DNA wraps around. If the way that DNA is wrapped around the histones changes, gene expression can change as well. Chromatin

2

From Wikipedia, the free encyclopedia
Although modifications occur throughout the histone sequence, the unstructured termini of histones (called histone tails) are particularly highly modified. These modifications include acetylation, methylation, ubiquitylation, phosphorylation and sumoylation. Acetylation is the most highly studied of these modifications. For example, acetylation of the K14 and K9 lysines of the tail of histone H3 by histone acetyltransferase enzymes (HATs) is generally correlated with transcriptional competence. One mode of thinking is that this tendency of acetylation to be associated with "active" transcription is biophysical in nature. Because it normally has a positively charged nitrogen at its end, lysine can bind the negatively charged phosphates of the DNA backbone and prevent them from repelling each other. The acetylation event converts the positively charged amine group on the side chain into a neutral amide linkage. This removes the positive charge, causing the DNA to repel itself. When this occurs, complexes like SWI/SNF and other transcriptional factors can bind to the DNA, thus opening it up and exposing it to enzymes like RNA polymerase so transcription of the gene can occur. In addition, the positively charged tails of histone proteins from one nucleosome may interact with the histone proteins on a neighboring nucleosome, causing them to pack closely. Lysine acetylation may interfere with these interactions, causing the chromatin structure to open up. Lysine acetylation may also act as a beacon to recruit other activating chromatin modifying enzymes (and basal transcription machinery as well). Indeed, the bromodomain — a protein segment (domain) that specifically binds acetyl-lysine — is found in many enzymes that help activate transcription, including the SWI/SNF complex (on the protein polybromo). It may be that acetylation acts in this and the previous way to aid in transcriptional activation. The idea that modifications act as docking modules for related factors is borne out by histone methylation as well. Methylation of lysine 9 of histone H3 has long been associated with constitutively transcriptionally silent chromatin (constitutive heterochromatin). It has been determined that a chromodomain (a domain that specifically binds methyl-lysine) in the transcriptionally repressive protein HP1 recruits HP1 to K9 methylated regions. One example that seems to refute this biophysical model for acetylation is that tri-methylation of histone H3 at lysine 4 is strongly associated with (and required for full) transcriptional activation. Tri-methylation in this case would introduce a fixed positive charge on the tail. It should be emphasized that differing histone modifications are likely to function in differing ways; acetylation at one position is likely to function differently than acetylation at another position. Also, multiple

Epigenetics
modifications may occur at the same time, and these modifications may work together to change the behavior of the nucleosome. The idea that multiple dynamic modifications regulate gene transcription in a systematic and reproducible way is called the histone code. DNA methylation frequently occurs in repeated sequences, and may help to suppress ’junk DNA’:[11] Because 5-methylcytosine is chemically very similar to thymidine, CpG sites are frequently mutated and become rare in the genome, except at CpG islands where they remain unmethylated. Epigenetic changes of this type thus have the potential to direct increased frequencies of permanent genetic mutation. DNA methylation patterns are known to be established and modified in response to environmental factors by a complex interplay of at least three independent DNA methyltransferases, DNMT1, DNMT3A and DNMT3B, the loss of any of which is lethal in mice.[12] DNMT1 is the most abundant methyltransferase in somatic cells,[13] localizes to replication foci,[14] has a 10–40-fold preference for hemimethylated DNA and interacts with the proliferating cell nuclear antigen (PCNA).[15] By preferentially modifying hemimethylated DNA, DNMT1 transfers patterns of methylation to a newly synthesized strand after DNA replication, and therefore is often referred to as the ‘maintenance’ methyltransferase.[16] DNMT1 is essential for proper embryonic development, imprinting and Xinactivation.[12][17] Chromosomal regions can adopt stable and heritable alternative states resulting in bistable gene expression without changes to the DNA sequence. Epigenetic control is often associated with alternative covalent modifications of histones. The stability and heritability of states of larger chromosomal regions are often thought to involve positive feedback where modified nucleosomes recruit enzymes that similarly modify nearby nucleosomes. A simplified stochastic model for this type of epigenetics is found here [18] . Because DNA methylation and chromatin remodeling play such a central role in many types of epigenic inheritance, the word "epigenetics" is sometimes used as a synonym for these processes. However, this can be misleading. Chromatin remodeling is not always inherited, and not all epigenetic inheritance involves chromatin remodeling.[19] It has been suggested that the histone code could be mediated by the effect of small RNAs. The recent discovery and characterization of a vast array of small (21- to 26-nt), non-coding RNAs suggests that there is an RNA component, possibly involved in epigenetic gene regulation. Small interfering RNAs can modulate transcriptional gene expression via epigenetic modulation of targeted promoters.[20]

3

From Wikipedia, the free encyclopedia

Epigenetics

RNA transcripts and their encoded proteins
Sometimes a gene, after being turned on, transcribes a product that (either directly or indirectly) maintains the activity of that gene. For example, Hnf4 and MyoD enhance the transcription of many liver- and muscle-specific genes, respectively, including their own, through the transcription factor activity of the proteins they encode. Other epigenetic changes are mediated by the production of different splice forms of RNA, or by formation of double-stranded RNA (RNAi). Descendants of the cell in which the gene was turned on will inherit this activity, even if the original stimulus for gene-activation is no longer present. These genes are most often turned on or off by signal transduction, although in some systems where syncytia or gap junctions are important, RNA may spread directly to other cells or nuclei by diffusion. A large amount of RNA and protein is contributed to the zygote by the mother during oogenesis or via nurse cells, resulting in maternal effect phenotypes. A smaller quantity of sperm RNA is transmitted from the father, but there is recent evidence that this epigenetic information can lead to visible changes in several generations of offspring.[21]

Structural inheritance systems
For more details on this topic, see Structural inheritance. In ciliates such as Tetrahymena and Paramecium, genetically identical cells show heritable differences in the patterns of ciliary rows on their cell surface. Experimentally altered patterns can be transmitted to daughter cells. It seems existing structures act as templates for new structures. The mechanisms of such inheritance are unclear, but reasons exist to assume that multicellular organisms also use existing cell structures to assemble new ones.[28]

Functions and consequences
Development
Somatic epigenetic inheritance, particularly through DNA methylation and chromatin remodeling, is very important in the development of multicellular eukaryotic organisms. The genome sequence is static (with some notable exceptions), but cells differentiate in many different types, which perform different functions, and respond differently to the environment and intercellular signalling. Thus, as individuals develop, morphogens activate or silence genes in an epigenetically heritable fashion, giving cells a "memory". In mammals, most cells terminally differentiate, with only stem cells retaining the ability to differentiate into several cell types ("totipotency" and "multipotency"). In mammals, some stem cells continue producing new differentiated cells throughout life, but mammals are not able to respond to loss of some tissues, for example, the inability to regenerate limbs, which some other animals are capable of. Unlike animals, plant cells do not terminally differentiate, remaining totipotent with the ability to give rise to a new individual plant. While plants do utilise many of the same epigenetic mechanisms as animals, such as chromatin remodeling, it has been hypothesised that plant cells do not have "memories", resetting their gene expression patterns at each cell division using positional information from the environment and surrounding cells to determine their fate.[29]

Prions
For more details on this topic, see Prions. Prions are infectious forms of proteins. Proteins generally fold into discrete units which perform distinct cellular functions, but some proteins are also capable of forming an infectious conformational state known as a prion. Although often viewed in the context of infectious disease, prions are more loosely defined by their ability to catalytically convert other native state versions of the same protein to an infectious conformational state. It is in this latter sense that they can be viewed as epigenetic agents capable of inducing a phenotypic change without a modification of the genome.[22] Fungal prions are considered epigenetic because the infectious phenotype caused by the prion can be inherited without modification of the genome. PSI+ and URE3, discovered in yeast in 1965 and 1971, are the two best studied of this type of prion.[23][24] Prions can have a phenotypic effect through the sequestration of protein in aggregates, thereby reducing that protein’s activity. In PSI+ cells, the loss of the Sup35 protein (which is involved in termination of translation) causes ribosomes to have a higher rate of read-through of stop codons, an effect which results in suppression of nonsense mutations in other genes.[25] The ability of Sup35 to form prions may be a conserved trait. It could confer an adaptive advantage by giving cells the ability to switch into a PSI+ state and express dormant genetic features normally terminated by premature stop codon mutations.[26][27]

Medicine
Epigenetics has many and varied potential medical applications. Congenital genetic disease is well understood, and it is also clear that epigenetics can play a role, for example, in the case of Angelman syndrome and PraderWilli syndrome. These are normal genetic diseases caused by gene deletions or inactivation of the genes, but are unusually common because individuals are essentially hemizygous because of genomic imprinting, and therefore a single gene knock out is sufficient to

4

From Wikipedia, the free encyclopedia
cause the disease, where most cases would require both copies to be knocked out.[30]

Epigenetics

Transgenerational epigenetic observations
Marcus Pembrey and colleagues also observed that the paternal (but not maternal) grandsons of Swedish boys who were exposed to famine in the 19th century were less likely to die of cardiovascular disease; if food was plentiful then diabetes mortality in the grandchildren increased, suggesting that this was a transgenerational epigenetic inheritance.[38]

Evolution
Although epigenetics in multicellular organisms is generally thought to be a mechanism involved in differentiation, with epigenetic patterns "reset" when organisms reproduce, there have been some observations of transgenerational epigenetic inheritance (e.g., the phenomenon of paramutation observed in maize). Although most of these multigenerational epigenetic traits are gradually lost over several generations, the possibility remains that multigenerational epigenetics could be another aspect to evolution and adaptation. These effects may require enhancements to the standard conceptual framework of the modern evolutionary synthesis.[31][32] Epigenetic features may play a role in short-term adaptation of species by allowing for reversible phenotype variability. The modification of epigenetic features associated with a region of DNA allows organisms, on a multigenerational time scale, to switch between phenotypes that express and repress that particular gene.[33] Whereas the DNA sequence of the region is not mutated, this change is reversible. It has also been speculated that organisms may take advantage of differential mutation rates associated with epigenetic features to control the mutation rates of particular genes.[33] Epigenetic changes have also been observed to occur in response to environmental exposure—for example, mice given some dietary supplements have epigenetic changes affecting expression of the agouti gene, which affects their fur color, weight, and propensity to develop cancer.[34][35]

Cancer and developmental abnormalities
A variety of compounds are considered as epigenetic carcinogens—they result in an increased incidence of tumors, but they do not show mutagen activity (toxic compounds or pathogens that cause tumors incident to increased regeneration should also be excluded). Examples include diethylstilbestrol, arsenite, hexachlorobenzene, and nickel compounds. Many teratogens exert specific effects on the fetus by epigenetic mechanisms.[39][40] While epigenetic effects may preserve the effect of a teratogen such as diethylstilbestrol throughout the life of an affected child, the possibility of birth defects resulting from exposure of fathers or in second and succeeding generations of offspring has generally been rejected on theoretical grounds and for lack of evidence.[41] However, a range of male-mediated abnormalities have been demonstrated, and more are likely to exist.[42] FDA label information for Vidaza(tm), a formulation of 5-azacitidine (an unmethylatable analog of cytidine that causes hypomethylation when incorporated into DNA) states that "men should be advised not to father a child" while using the drug, citing evidence in treated male mice of reduced fertility, increased embryo loss, and abnormal embryo development. In rats, endocrine differences were observed in offspring of males exposed to morphine.[43] In mice, second generation effects of diethylstilbesterol have been described occurring by epigenetic mechanisms.[44] In 2008, the National Institutes of Health announced that $190 million had been earmarked for epigenetics research over the next five years. In announcing the funding, government officials noted that epigenetics has the potential to explain mechanisms of aging, human development, and the origins of cancer, heart disease, mental illness, as well as several other conditions. Some investigators, like Randy Jirtle, PhD, of Duke University Medical Center, think epigenetics may ultimately turn out to have a greater role in disease than genetics.[45]

Epigenetic effects in humans
Genomic imprinting and related disorders
Some human disorders are associated with genomic imprinting, a phenomenon in mammals where the father and mother contribute different epigenetic patterns for specific genomic loci in their germ cells.[36] The most well-known case of imprinting in human disorders is that of Angelman syndrome and Prader-Willi syndrome—both can be produced by the same genetic mutation, chromosome 15q partial deletion, and the particular syndrome that will develop depends on whether the mutation is inherited from the child’s mother or from their father.[37] This is due to the presence of genomic imprinting in the region. Beckwith-Wiedemann syndrome is also associated with genomic imprinting, often caused by abnormalities in maternal genomic imprinting of a region on chromosome 11.

5

From Wikipedia, the free encyclopedia

Epigenetics
• R. J. Sims III, K. Nishioka and D. Reinberg (2003) Histone lysine methylation: a signature for chromatin function. Trends Genet. 19, 629-637. • Rupert Sheldrake, A New Biology, morphogenetic fields. • B. D. Strahl and C. D. Allis (2000) The language of covalent histone modifications. Nature 403, 41-45. • C.H. Waddington (1942), The epigenotype. Endeavour 1, 18–20. • B. McClintock (1978) Mechanisms that Rapidly Reorganize the Genome. Stadler Symposium vol 10:25-48 • G.W. Grimes; K.J. Aufderheide; Cellular Aspects of Pattern Formation: the Problem of Assembly. Monographs in Developmental Biology, Vol. 22. Karger, Basel (1991) • Eva Jablonka and Marion J. Lamb Evolution in Four Dimensions: Genetic, Epigenetic, Behavioral, and Symbolic Variation in the History of Life The MIT Press (2005) ISBN 978-0262101073 • Article on The Philosophy of Molecular and Developmental Biology to appear in Blackwell’s Guide to Philosophy of Science,. P.K. Machamer and M. Silberstein (Eds). • Epigenetics edited by C. David Allis, Thomas Jenuwein, Danny Reinberg, and Marie-Laure Caparros. Cold Spring Harbor Press, 2007. • Evolution by Nicholas Barton, Derek Briggs, Jonathan Eisen, David Goldstein, and Nipam Patel. Cold Spring Harbor Press, 2007. • Chromatin and Gene Regulation: Mechanisms in Epigenetics by Bryan Turner. Blackwell Publishing, 2002. • Epigenetics edited by J. Tost. Caister Academic Press, 2008. • RNA and the Regulation of Gene Expression: A Hidden Layer of Complexity edited by K. V. Morris. Caister Academic Press, 2008. • Epigenetic biomarkers in psychiatric disorders British Journal of Pharmacology (2008) 155, 795–796; doi:10.1038/bjp.2008.254; published online 23 June 2008

Twin studies
Recent studies involving both dizogotic and monozygotic twins have produced some evidence of epigenetic influence in humans.[46][47][48]

Epigenetics in microorganisms
Bacteria make widespread use of postreplicative DNA methylation for the epigenetic control of DNA-protein interactions. Bacteria make use of DNA adenine methylation (rather than DNA cytosine methylation) as an epigenetic signal. DNA adenine methylation is important in bacteria virulence in organisms such as Escherichia coli, Salmonella, Vibrio, Yersinia, Haemophilus, and Brucella. In Alphaproteobacteria, methylation of adenine regulates the cell cycle and couples gene transcription to DNA replication. In Gammaproteobacteria, adenine methylation provides signals for DNA replication, chromosome segregation, mismatch repair, packaging of bacteriophage, transposase activity and regulation of gene expression.[49][50] The yeast prion PSI is generated by a conformational change of a translation termination factor, which is then inherited by daughter cells. This can provide a survival advantage under adverse conditions. This is an example of epigenetic regulation enabling unicellular organisms to respond rapidly to environmental stress. Prions can be viewed as epigenetic agents capable of inducing a phenotypic change without modification of the genome.[50]

See also
• • • • • • • • • • Epigenetic Theory Baldwinian evolution Barbara McClintock Centromere Evolutionary developmental psychology Histone code Molecular biology Somatic epitype Synthetic genetic array Weismann barrier

Further reading
• Oskar Hertwig, 1849-1922. Biological problem of today: preformation or epigenesis? The basis of a theory of organic development. W. Heinemann: London, 1896. • Rudolf Jaenisch and A. Bird (2003) Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals. Nat. Genet. 33 (Suppl) 245-254. • Joshua Lederberg,The Meaning of Epigenetics, The Scientist 15(18):6, Sep. 17, 2001.

Notes and references
[1] [2] [3] Adrian Bird (2007). "Perceptions of epigenetics". Nature 447: 396–398. doi:10.1038/nature05913. PMID 17522671 Special report: ’What genes remember’ by Philip Hunter | Prospect Magazine May 2008 issue 146 Reik, Wolf (2007-05-23). "Stability and flexibility of epigenetic gene regulation in mammalian development". Nature 447 (May (online)): 425–432. doi:10.1038/ nature05918. http://www.nature.com/nature/journal/ v447/n7143/full/nature05918.html. Retrieved on 2008-04-05.

6

From Wikipedia, the free encyclopedia
[4]

Epigenetics

[5] [6]

[7]

[8] [9] [10]

[11]

[12]

[13]

[14]

[15]

[16]

[17]

Roloff, T.C., Nuber, U.A., 2005 Chromatin , [18] I.B. Dodd, M.A. Micheelsen, K. Sneppen and G. Thon epigenetics and stem cells. Eur J Cell Biol. 84, (2007). Theoretical Analysis of Epigenetic Cell 123-135 Memory by Nucleosome Modification Cell C.H. Waddington (1942) (1977). "The epigenotype". 129:813-822. Endeavour 1: 18–20. doi:10.1016/0160-9327(77)90005-9. [19] Mark Ptashne, 2007. On the use of the word ‘epigenetic’. Current Biology, 17(7):R233-R236. Holliday, R., 1990. Mechanisms for the control of gene activity during development. Biol. Rev. doi:10.1016/j.cub.2007.02.030 Cambr. Philos. Soc. 65, 431-471 [20] Morris KV (2008). "Epigenetic Regulation of Gene Russo, V.E.A., Martienssen, R.A., Riggs, A.D., 1996 Expression". RNA and the Regulation of Gene Expression: Epigenetic mechanisms of gene regulation. Cold A Hidden Layer of Complexity. Caister Academic Press. Spring Harbor Laboratory Press, Plainview, NY. ISBN 978-1-904455-25-7. Epigenetics [21] Choi CQ (2006-05-25). "The Scientist: RNA can be V.L. Chandler (2007). "Paramutation: From Maize to hereditary molecule". The Scientist. http://www.theMice". Cell 128: 641–645. doi:10.1016/j.cell.2007.02.007. scientist.com/news/display/23494. Retrieved on 2006. Jablonka, E; Lamb MJ and Lachmann M (September [22] A. Yool and W.J. Edmunds (1998). "Epigenetic inheritance 1992). "Evidence, mechanisms and models for the and prions". Journal of Evolutionary Biology 11: 241–242. inheritance of acquired characteristics". J. Theoret. Biol. doi:10.1007/s000360050085. 158 (2): 245–268. doi:10.1016/S0022-5193(05)80722-2. [23] B.S. Cox (1965). "[PSI], a cytoplasmic suppressor of superhttp://www.sciencedirect.com/ suppression in yeast". Heredity 20: 505–521. doi:10.1038/ science?_ob=ArticleURL&_udi=B6WMD-4KFTYG9-8&_user=10&_handle=Chdy.1965.65. WA-A-E-E-MsSAYWW-UUW-U-U-E-U-U-AAZEEUZCDZ[24] F. Lacroute (1971). "Non-Mendelian mutation allowing AAZDVYDBDZ-ADYZVZWEA-Eureidosuccinic acid uptake in yeast". Journal of U&_fmt=summary&_coverDate=09%2F21%2F1992&_rdoc=8&_orig=browse&_srch=%23toc%236932%231992%23998419997%23628456!&_cdi=6932 Bacteriology 106: 519–522. Chédin, F (1992). "The Chedin Laboratory". [25] S.W. Liebman and F. Sherman (1979). http://www.mcb.ucdavis.edu/faculty-labs/chedin/ "Extrachromosomal psi+ determinant suppresses research.htm. Retrieved on 2006-12-28. nonsense mutations in yeast". Journal of Bacteriology 139 ^ Li, E; Bestor TH and Jaenisch R (June 1992). "Targeted (3): 1068–1071. Free full text available mutation of the DNA methyltransferase gene results in [26] H.L. True and S.L. Lindquist (2000). "A yeast prion embryonic lethality". Cell 69 (6): 915–926. doi:10.1016/ provides a mechanism for genetic variation and 0092-8674(92)90611-F. http://www.sciencedirect.com/ phenotypic diversity". Nature 407: 477–483. doi:10.1038/ science?_ob=ArticleURL&_udi=B6WSN-4D57093-1R&_coverDate=06%2F12%2F1992&_alid=515191593&_rdoc=1&_fmt=&_orig=search&_qd=1&_ 35035005. Robertson, KD; Uzyolgi E, Lian G et al. (June 1999). "The [27] J. Shorter and S. Lindquist (2005). "Prions as adaptive human DNA methyltransferases (DNMTs) 1, 3a, 3b: conduits of memory and inheritance". Nature Reviews Coordinate mRNA expression in normal tissues and Genetics 6 (6): 435–450. doi:10.1038/nrg1616. overexpression in tumors". Nucleic Acids Res 27 (11): [28] Oyama, Susan; Paul E. Griffiths, Russell D. Gray (2001). 2291–2298. doi:10.1093/nar/27.11.2291. PMID 10325416. Cycles of Contingency: Developmental Systems and http://www.pubmedcentral.nih.gov/ Evolution. MIT Press. ISBN 0262650630. articlerender.fcgi?tool=pubmed&pubmedid=10325416. [29] Silvia Costa and Peter Shaw. 2006. ’Open Minded’ Leonhardt, H; Page AW, Weier HU, Bestor TH (November cells: how cells can change fate. Trends in Cell 1992). "A targeting sequence directs DNA Biology 17(3):101-106. doi:10.1016/j.tcb.2006.12.005 methyltransferase to sites of DNA replication in [30] Online ’Mendelian Inheritance in Man’ (OMIM) mammalian nuclei". Cell 71 (5): 865–873. doi:10.1016/ 105830 0092-8674(92)90561-P. http://www.sciencedirect.com/ [31] Jablonka, Eva; Marion J. Lamb (2005). Evolution in Four science?_ob=ArticleURL&_udi=B6WSN-4D0YB27-19&_coverDate=11%2F27%2F1992&_alid=515194074&_rdoc=1&_fmt=&_orig=search&_qd=1&_ Dimensions. MIT Press. ISBN 0-262-10107-6. Chuang, LS; Ian HI, Koh TW et al. (September 1997). [32] See also Denis Noble The Music of Life see esp pp93-8 "Human DNA-(cytosine-5) methyltransferase-PCNA and p48 where he cites Jablonka & Lamb and complex as a target for p21WAF1". Science 277 (5334): Massimo Pigliucci’s review of Jablonka and Lamb in 1996–2000. doi:10.1126/science.277.5334.1996. PMID Nature 435, 565-566 (2 June 2005) [33] ^ O.J. Rando and K.J. Verstrepen (2007). "Timescales of 9302295. Genetic and Epigenetic Inheritance". Cell 128: 655–668. Robertson, KD; Wolffe AP (October 2000). "DNA doi:10.1016/j.cell.2007.01.023. methylation in health and disease". Nat Rev Genet 1 (1): [34] Cooney, CA, Dave, AA, and Wolff, GL (2002). "Maternal 11–19. doi:10.1038/35049533. http://www.nature.com/ Methyl Supplements in Mice Affect Epigenetic Variation nrg/journal/v1/n1/abs/nrg1000_011a_fs.html. and DNA Methylation of Offspring". Journal of Nutrition Li, E; Beard C and Jaenisch R (December 1993). "Role for 132: 2393S–2400S. available online DNA methylation in genomic imprinting". Nature 366 (6453): 362–365. doi:10.1038/366362a0.

7

From Wikipedia, the free encyclopedia

Epigenetics

[35] Waterland RA and Jirtle RL (August 2003). "Transposable [43] Cicero, TJ; Adams NL, Giodarno A et al. (March 1991). elements: Targets for early nutritional effects on "Influence of morphine exposure during adolescence on epigenetic gene regulation". Molecular and Cellular the sexual maturation of male rats and the development Biology 23 (15): 5293–5300. doi:10.1128/ of their offspring". J Pharmacol Exp Ther. 256 (3): MCB.23.15.5293-5300.2003. PMID 12861015. 1086–1093. http://www.ncbi.nlm.nih.gov/entrez/ http://mcb.asm.org/cgi/content/full/23/15/5293. query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=200 [36] A.J. Wood and A.J. Oakey (2006). "Genomic imprinting in [44] Newbold, RR; Padilla-Banks E and Jefferson WN (June mammals: Emerging themes and established theories". 2006). "Adverse effects of the model environmental PLOS Genetics 2 (11): 1677–1685. doi:10.1371/ estrogen diethylstilbestrol are transmitted to subsequent journal.pgen.0020147. available online generations". Endocrinology 147 (6 Suppl): S11–S17. [37] J.H.M. Knoll, R.D. Nicholls, R.E. Magenis, J.M. Graham Jr, doi:10.1210/en.2005-1164. PMID 16690809. M. Lalande, S.A. Latt (1989). "Angelman and Prader-Willi [45] Beil, Laura (Winter, 2008). "Medicine’s New Epicenter? syndromes share a common chromosome deletion but Epigenetics: New field of epigenetics may hold the secret differ in parental origin of the deletion". American to flipping cancer’s "off" switch.". CURE (Cancer Updates, Journal of Medical Genetics 32: 285–290. doi:10.1002/ Research and Education). http://www.curetoday.com/ ajmg.1320320235. index.cfm/fuseaction/article.show/id/2/article_id/949. [38] Pembrey ME, Bygren LO, Kaati G, et al.. Sex-specific, [46] "The Claim: Identical Twins Have Identical DNA". New male-line transgenerational responses in humans. York Times. 2008. http://www.nytimes.com/2008/03/11/ Eur J Hum Genet 2006; 14: 159-66. PMID 16391557. health/11real.html. Robert Winston refers to this study in a lecture; see [47] Kaminsky, Zachary A (2009). "DNA methylation profiles also discussion at Leeds University, here in monozygotic and dizygotic twins". Nature Genetics 41: [39] Bishop, JB; Witt KL and Sloane RA (December 1997). 240. doi:10.1038/ng.286. "Genetic toxiticities of human teratogens". Mutat Res 396 [48] Fraga, M. F. (2005). "Epigenetic differences arise during (1-2): 9–43. http://www.sciencedirect.com/ the lifetime of monozygotic twins". Proceedings of the science?_ob=ArticleURL&_udi=B6T2C-3TGW0WR-19&_coverDate=12%2F12%2F1997&_alid=515200131&_rdoc=1&_fmt=&_orig=search&_qd=1& National Academy of Sciences 102: 10604. doi:10.1073/ [40] Gurvich, N; Berman MG, Wittner BS et al. (July 2004). pnas.0500398102. http://www.pnas.org/content/102/30/ "Association of valproate-induced teratogenesis with 10604.full. histone deacetylase inhibition in vivo". Faseb J 19 (9): [49] Casadesus J and Low D (September 2006). "Epigenetic 1166–1168. doi:10.1096/fj.04-3425fje. PMID 15901671. Gene Regulation in the Bacterial World". Microbiol Mol http://www.fasebj.org/cgi/reprint/04-3425fjev1. Biol Rev 70 (3): 830–856. doi:10.1128/MMBR.00016-06. [41] Smithells, D (November 1998). "Does thalidomide cause [50] ^ Tost J (editor). (2008). Epigenetics. Caister Academic second generation birth defects?". Drug Saf 19 (5): Press. ISBN 978-1-904455-23-3 . 339–341. doi:10.2165/00002018-199819050-00001. http://www.horizonpress.com/epi. http://www.ncbi.nlm.nih.gov/entrez/ query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=9825947. [42] Friedler, G (December 1996). "Paternal exposures: impact • DNA Is Not Destiny - Discover Magazine cover story on reproductive and developmental outcome. An • BBC - Horizon - 2005 - The Ghost In Your Genes overview". Pharmacol Biochem Behav 55 (4): 691–700. • Epigenetics article at Hopkins Medicine doi:10.1016/S0091-3057(96)00286-9. http://www.ncbi.nlm.nih.gov/entrez/ query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=8981601.

External links

Retrieved from "http://en.wikipedia.org/wiki/Epigenetics" Categories: Epigenetics This page was last modified on 17 May 2009, at 00:31 (UTC). All text is available under the terms of the GNU Free Documentation License. (See Copyrights for details.) Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc., a U.S. registered 501(c)(3) tax-deductible nonprofit charity. Privacy policy About Wikipedia Disclaimers

8


				
DOCUMENT INFO
Shared By:
Categories:
Tags:
Stats:
views:85
posted:5/18/2009
language:English
pages:8