DOCSLIB.ORG

Genomic Imprinting in Mammals: Its Life Cycle, Molecular Mechanisms and Reprogramming

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Genomic Imprinting in Mammals: Its Life Cycle, Molecular Mechanisms and Reprogramming npg Genomic imprinting and reprogramming Cell Research (2011) 21:466-473. 466 © 2011 IBCB, SIBS, CAS All rights reserved 1001-0602/11 $ 32.00 npg REVIEW www.nature.com/cr Genomic imprinting in mammals: its life cycle, molecular mechanisms and reprogramming Yufeng Li1, Hiroyuki Sasaki1 1Division of Epigenomics, Department of Molecular Genetics, Medical Institute of Bioregulation, Kyushu University, 3-1-1 Mai- dashi, Higashi-ku, Fukuoka 812-8582, Japan Genomic imprinting, an epigenetic gene-marking phenomenon that occurs in the germline, leads to parental-ori- gin-specific expression of a small subset of genes in mammals. Imprinting has a great impact on normal mammalian development, fetal growth, metabolism and adult behavior. The epigenetic imprints regarding the parental origin are established during male and female gametogenesis, passed to the zygote through fertilization, maintained throughout development and adult life, and erased in primordial germ cells before the new imprints are set. In this review, we focus on the recent discoveries on the mechanisms involved in the reprogramming and maintenance of the imprints. We also discuss the epigenetic changes that occur at imprinted loci in induced pluripotent stem cells. Keywords: genomic imprinting; reprogramming; DNA methylation; DNA demethylation; histone modification Cell Research (2011) 21:466-473. doi:10.1038/cr.2011.15; published online 1 February 2011 Introduction maternal allele [4]. To date, more than 100 imprinted genes have been identified in mice (http://www.mouse- In diploid organisms, the maternal and paternal alleles book.org/catalog.php?catalog=imprinting), and many of most autosomal genes are expressed at similar levels, of them are also imprinted in humans [5]. All imprinted and thus contribute equally to the phenotype. However, genes show either maternal-specific or paternal-specific in eutherian mammals (such as humans and mice) and mono-allelic expression, and their proper expression is marsupials, the parental alleles are not always function- essential for normal development, fetal growth, nutrient ally equivalent. This was first discovered in early 1980s metabolism and adult behavior. In humans, genetic and by embryological studies in mice: nuclear transfer ex- epigenetic disturbances in expression of the imprinted periments using pronuclear stage embryos showed that genes can cause well-known malformation disorders, reconstituted embryos with two maternal genomes and such as Prader-Willi syndrome, Angelman syndrome, no paternal complement and those with two paternal Beckwith-Wiedemann syndrome and Silver-Russell syn- genomes and no maternal complement never survive drome [5-7]. beyond mid-gestation. This suggested that the parental Most of the imprinted genes are found in clusters in genomes are functionally non-equivalent and marked or the genome, corresponding to the specific chromosomal imprinted differently during male and female gameto- segments identified by the above genetic studies. Such genesis [1, 2]. Almost at the same time, genetic experi- imprinted clusters often span hundreds to thousands of ments using chromosome translocations in mice showed kilobases. A given imprinted cluster can comprise both that specific chromosomal segments, but not the entire paternally and maternally expressed imprinted genes, genome, function differently depending on the parental some of which correspond to non-coding RNAs, and also origin [3]. Then, mouse Igf2r was identified as the first non-imprinted genes [8-10]. The clusters also contain imprinted gene in 1991: it was expressed only from the CpG-rich regions that are DNA-methylated only on one of the two parental chromosomes (differentially methy- lated regions, DMRs). At some DMRs, differential DNA methylation is also observed between sperm and oocytes, Correspondence: Hiroyuki Sasaki Fax: +81-92-642-6799 and therefore gametic in origin. These DMRs are called E-mail: [email protected] germline or gametic DMRs. In some cases, there is evi- Cell Research | Vol 21 No 3 | March 2011 Yufeng Li and Hiroyuki Sasaki npg 467 dence that the germline DMR functions as an imprinting control region, which controls the mono-allelic expres- sion of the imprinted genes and the methylation status of the other DMRs within the cluster [11]. Most of the germline DMRs are methylated in the female germline and only four DMRs (H19, Dlk1-Gtl2, Rasgrf1 and Zdbf2) are known to be methylated in the male germline [12, 13]. Importantly, mutations in the maintenance DNA methyltranferase DNMT1 disrupt the parental-origin- specific expression patterns of the imprinted genes in mouse embryos [14]. In addition to DNA methylation, other epigenetic modifications and factors, such as his- tone modifications, insulator proteins (such as CTCF) and long non-coding RNAs, are also involved in imprint- Figure 1 Life cycle of the genomic imprints. The paternal (blue) ing. and maternal imprints (red) are established in the germ-line The epigenetic modifications including DNA methyla- and maintained through fertilization and subsequent embryonic tion at the germline DMRs undergo dynamic reprogram- development. However, the imprints are erased in PGCs before ming during germ cell development but, on the other hand, the new imprints are set. The imprints need to be maintained during the extensive reprogramming that occurs in animal they are maintained and faithfully propagated throughout cloning and iPS cell generation (blue arrow). embryonic development [11, 15, 16]. The whole process is complex and regulated tightly. In this study, we review the recent discoveries on the mechanisms involved in the establishment, maintenance and erasure of the epigenetic tablished in the germline are transmitted to the zygote imprints. We also discuss the epigenetic changes ob- through fertilization and maintained faithfully throughout served at imprinted gene clusters in induced pluripoten- the development and adult life. Notably, the methylation tial stem (iPS) cells. imprints at the germline DMRs escape from the global epigenetic reprogramming that occurs in pre-implanta- Life cycle of the genomic imprints tion embryos [11, 16, 25]. The reprogramming at this stage includes the replacement of protamines by histones The life cycle of the genomic imprints in mammals in the paternal genome, active demethylation of the pa- is schematically shown in Figure 1. The cycle consists ternal genome [26] and subsequent passive demethyla- of three major steps: establishment, maintenance and tion of both parental genomes [27, 28]. After implanta- erasure, all of which are important for this biological tion, the differential methylation at the germline DMRs phenomenon. The establishment of the epigenetic im- has to survive another global epigenetic change, i.e., de prints occurs in male and female germ cells. In the male novo DNA methylation. While many genes including the germline, de novo DNA methylation of the four pater- pluripotency genes and germ-cell-specific genes become nally methylated germline DMRs occurs progressively highly methylated in early post-implantation embryos, in mitotically arrested (G1/G0) prospermatogonia (or the unmethylated allele of the DMR has to be protected gonocytes) after embryonic day 14.5 (E14.5). Then, the from this strong wave of de novo DNA methylation. In paternal methylation imprints become fully established fact, imprint maintenance is critical for the parental- in prospermatogonia by the neonatal stage [17-21]. In origin-specific mono-allelic expression of the imprinted the female germline, de novo DNA methylation initiates genes throughout development. asynchronously at different germline DMRs during the The last step of the imprint life cycle is the erasure of oocyte growth phase [22, 23]. Growing oocytes are at the the epigenetic imprints in primordial germ cells (PGCs): diplotene/dictyate stage of meiotic prophase I, and the this ensures the sex-dependent imprint establishment in maternal methylation imprints become fully established later stages of germ cell development described above. by the fully grown oocyte stage [22, 23]. The establish- PGCs are specified from the epiblast cells of early post- ment of the maternal methylation imprints is correlated implantation embryos. Then, PGCs proliferate actively, with the establishment of the functional imprints, which followed by migration to the genital ridge, the precursor was shown by the developmental potential of nuclear of the gonads, between E7.25 and E10.5. In this period, transferred bi-maternal embryos [24]. the genome of the PGCs undergoes epigenetic repro- The paternal and maternal epigenetic imprints es- gramming to restore pluripotency [25, 29, 30], but they www.cell-research.com | Cell Research 468 npg Genomic imprintingandreprogramming Table 1 Factors involved in the life cycle of the genomic imprints Step of the cycle Factor name Biochemical function Germ-line DMRs affected in knockout Reference Paternally methylated Maternally methylated DNMT3A de novo DNA methy- H19, Dlk1-Gtl2, Zdbf2, Rasgrf1 Snrpn, Peg1(Mest), Peg3, Igf2r [20, 21, 37-39] ltransferase DNMT3B Rasgrf1 [20, 38, 39] Establishment DNMT3L Cofactor of DNMT3A H19, Dlk1-Gtl2, Rasgrf1 Snrpn, Peg1, Peg3, Igf2r [20, 36, 38, 39 ,40] and DNMT3B KDM1B Histone H3K4 demethylase Peg1, Grb10, Zac1(Plagl1), Impact [45] ZFP57 KRAB zinc finger protein Snrpn [46] DNMT1 Maintenance DNA methy- H19, Rasgrf1 Igf2r, Peg3, Snrpn [14, 48-50] (DNMT1o ltransferase and DNMT1s) Maintenance ZFP57 KRAB zinc finger protein
Load more

Recommended publications
  • Key Features of Genomic Imprinting During Mammalian Spermatogenesis
    ogy: iol Cu ys r h re P n t & R y e s Anatomy & Physiology: Current m e o a t r a c n h Štiavnická et al., Anat Physiol 2016, 6:5 A Research ISSN: 2161-0940 DOI: 10.4172/2161-0940.1000236 Review Article Open Access Key Features of Genomic Imprinting during Mammalian Spermatogenesis: Perspectives for Human assisted Reproductive Therapy: A Review Miriama Štiavnická*1,2, Olga García Álvarez1, Jan Nevoral1,2, Milena Králíčková1,2 and Peter Sutovsky3,4 1Laboratory of Reproductive Medicine, Biomedical Centre, Department of Histology and Embryology, Charles University in Prague, Czech Republic 2Department of Histology and Embryology, Charles University in Prague, Czech Republic 3Division of Animal Science, and Departments of Obstetrics, Gynecology and Women’s Health, University of Missouri, Columbia, MO, USA 4Departments of Obstetrics, Gynaecology and Women’s Health, University of Missouri, Columbia, MO, USA *Corresponding author: Miriama Štiavnická, Laboratory of Reproductive Medicine, Biomedical Centre, Department of Histology and Embryology, Charles University in Prague, Czech Republic, Tel: +420377593808; E-mail: [email protected] Received date: June 23, 2016; Accepted date: August 16, 2016; Published date: August 23, 2016 Copyright: © 2016 Štiavnická M, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Abstract Increasing influence of epigenetics is obvious in all medical fields including reproductive medicine. Epigenetic alterations of the genome and associated post-translational modifications of DNA binding histones equally impact gamete development and maturation, as well as embryogenesis.
    [Show full text]
  • Genomic Imprinting, Action, and Interaction of Maternal and Fetal Genomes
    Genomic imprinting, action, and interaction of maternal and fetal genomes Eric B. Keverne1 Sub-Department of Animal Behaviour, University of Cambridge, Cambridge CB23 8AA, United Kingdom Edited by Donald W. Pfaff, The Rockefeller University, New York, NY, and approved October 16, 2014 (received for review July 9, 2014) Mammalian viviparity (intrauterine development of the fetus) and striatum (4). Moreover, the growth of the brain in parthe- introduced a new dimension to brain development, with the fetal nogenetic chimeras was enhanced by this increased gene dosage hypothalamus and fetal placenta developing at a time when the from maternally expressed alleles, whereas the brains of an- fetal placenta engages hypothalamic structures of the maternal drogenetic chimeras were smaller, especially relative to body generation. Such transgenerational interactions provide a basis for weight (3). These spatially distinct anatomical outcomes matched ensuring optimal maternalism in the next generation. This success to those brain regions found to be affected in human clinical has depended on genomic imprinting and a biased role of the studies on brain dysfunction seen in Prader–Willi and Angelman’s matriline. Maternal methylation imprints determine parent of origin syndromes (5, 6). The uniparental disomies of restricted chromo- expression of genes fundamental to both placental and hypotha- somal regions found in these clinical disorders were congruent lamic development. The matriline takes a further leading role for with the neural distribution of the chimeric cells. transgenerational reprogramming of these imprints. Developmen- Since these early findings, ∼100 genes have been identified tal errors are minimized by the tight control that imprinted genes to be “imprinted,” the majority of which have been shown to be have on regulation of downstream evolutionary expanded gene expressed in the placenta (7).
    [Show full text]
  • Genomic Imprinting : a General Overview
    Vol. 8(2), pp. 18-34, October 2013 DOI: 10.5897/BMBR07.003 ISSN 1538-2273 © 2013 Academic Journals Biotechnology and Molecular Biology Reviews http://www.academicjournals.org/BMBR Review Genomic imprinting: A general overview Muniswamy K.1* and Thamodaran P.2 1Division of Veterinary Biotechnology, Indian Veterinary Research Institute, Izatnagar- 243 122, India. 2Division of Veterinary Microbiology, TANUVAS, Chennai-600 007, India. Accepted 27 August, 2013 Usually, most of the genes are biallelically expressed but imprinted gene exhibit monoallelic expression based on their parental origin. Genomic imprinting exhibit differences in control between flowering plants and mammals, for instance, imprinted gene are specifically activated by demethylation, rather than targeted for silencing in plants and imprinted gene expression in plant which occur in endosperm. It also displays sexual dimorphism like differential timing in imprint establishment and RNA based silencing mechanism in paternally repressed imprinted gene. Within imprinted regions, the unusual occurrence and distribution of various types of repetitive elements may act as genomic imprinting signatures. Imprinting regulation probably at many loci involves insulator protein dependent and higher-order chromatin interaction, and/or non-coding RNAs mediated mechanisms. However, placenta- specific imprinting involves repressive histone modifications and non-coding RNAs. The higher-order chromatin interaction involves differentially methylated domains (DMDs) exhibiting sex-specific methylation that act as scaffold for imprinting, regulate allelic-specific imprinted gene expression. The paternally methylated differentially methylated regions (DMRs) contain less CpGs than the maternally methylated DMRs. The non-coding RNAs mediated mechanisms include C/D RNA and microRNA, which are invovled in RNA-guided post-transcriptional RNA modifications and RNA-mediated gene silencing, respectively.
    [Show full text]
  • Environmental Exposure to Endocrine Disrupting Chemicals Influences Genomic Imprinting, Growth, and Metabolism
    G C A T T A C G G C A T genes Review Environmental Exposure to Endocrine Disrupting Chemicals Influences Genomic Imprinting, Growth, and Metabolism Nicole Robles-Matos 1, Tre Artis 2 , Rebecca A. Simmons 3 and Marisa S. Bartolomei 1,* 1 Epigenetics Institute, Center of Excellence in Environmental Toxicology, Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, 9-122 Smilow Center for Translational Research, Philadelphia, PA 19104, USA; [email protected] 2 Division of Hematology/Oncology, Boston Children’s Hospital, Harvard Medical School, Boston, MA 02115, USA; [email protected] 3 Center of Excellence in Environmental Toxicology, Department of Pediatrics, Children’s Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, 1308 Biomedical Research Building II/III, Philadelphia, PA 19104, USA; [email protected] * Correspondence: [email protected] Abstract: Genomic imprinting is an epigenetic mechanism that results in monoallelic, parent-of- origin-specific expression of a small number of genes. Imprinted genes play a crucial role in mam- malian development as their dysregulation result in an increased risk of human diseases. DNA methylation, which undergoes dynamic changes early in development, is one of the epigenetic marks regulating imprinted gene expression patterns during early development. Thus, environmental insults, including endocrine disrupting chemicals during critical periods of fetal development, can alter DNA methylation patterns, leading to inappropriate developmental gene expression and disease risk. Here, we summarize the current literature on the impacts of in utero exposure to endocrine disrupting chemicals on genomic imprinting and metabolism in humans and rodents. We evaluate Citation: Robles-Matos, N.; Artis, T.; Simmons, R.A.; Bartolomei, M.S.
    [Show full text]
  • Genomic Imprinting: Employing and Avoiding Epigenetic Processes
    Downloaded from genesdev.cshlp.org on October 3, 2021 - Published by Cold Spring Harbor Laboratory Press REVIEW Genomic imprinting: employing and avoiding epigenetic processes Marisa S. Bartolomei1 Department of Cell and Developmental Biology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA Genomic imprinting refers to an epigenetic mark that genomic_imprinting for a full list), with the imprinting distinguishes parental alleles and results in a monoallelic, of many of these genes conserved in humans (http:// parental-specific expression pattern in mammals. Few www.otago.ac.nz/IGC). Although additional genes and phenomena in nature depend more on epigenetic mech- transcripts may be discovered using more modern se- anisms while at the same time evading them. The alleles quence analysis of transcriptomes, it is notable that the of imprinted genes are marked epigenetically at discrete first few published studies of this nature reported only elements termed imprinting control regions (ICRs) with a small number of novel imprinted genes, suggesting that their parental origin in gametes through the use of DNA many new widely expressed imprinted genes are not methylation, at the very least. Imprinted gene expression likely to be identified (Babak et al. 2008; Wang et al. is subsequently maintained using noncoding RNAs, 2008). Nevertheless, more detailed, allele-specific tran- histone modifications, insulators, and higher-order chro- scriptome analyses of purified cell populations should add matin structure. Avoidance is manifest when imprinted to the growing list of tissue-specific imprinted genes. genes evade the genome-wide reprogramming that oc- Imprinted genes have a variety of functions; many curs after fertilization and remain marked with their imprinted genes are important for fetal and placental parental origin.
    [Show full text]
  • Imprinted Genes and Multiple Sclerosis: What Do We Know?
    International Journal of Molecular Sciences Review Imprinted Genes and Multiple Sclerosis: What Do We Know? Natalia Baulina 1,2,* , Ivan Kiselev 1 and Olga Favorova 1,2 1 Institute of Translational Medicine, Pirogov Russian National Research Medical University, 117997 Moscow, Russia; [email protected] (I.K.); [email protected] (O.F.) 2 Center for Precision Genome Editing and Genetic Technologies for Biomedicine, Pirogov Russian National Research Medical University, 117997 Moscow, Russia * Correspondence: [email protected] Abstract: Multiple sclerosis (MS) is a chronic autoimmune neurodegenerative disease of the central nervous system that arises from interplay between non-genetic and genetic risk factors. The epige- netics functions as a link between these factors, affecting gene expression in response to external influence, and therefore should be extensively studied to improve the knowledge of MS molecular mechanisms. Among others, the epigenetic mechanisms underlie the establishment of parent-of- origin effects that appear as phenotypic differences depending on whether the allele was inherited from the mother or father. The most well described manifestation of parent-of-origin effects is genomic imprinting that causes monoallelic gene expression. It becomes more obvious that dis- turbances in imprinted genes at the least affecting their expression do occur in MS and may be involved in its pathogenesis. In this review we will focus on the potential role of imprinted genes in MS pathogenesis. Keywords: multiple sclerosis; parent-of-origin effect; genomic imprinting; DLK1-DIO3 locus; miRNA Citation: Baulina, N.; Kiselev, I.; 1. Introduction Favorova, O. Imprinted Genes and Multiple Sclerosis: What Do We Multiple sclerosis (MS) is a chronic autoimmune and neurodegenerative disease of Know? Int.
    [Show full text]
  • A Model System to Study Genomic Imprinting of Human Genes (Beckwith–Weidemann Syndrome͞gene Expression͞imprinting͞methylation͞prader–Willi Syndrome)
    Proc. Natl. Acad. Sci. USA Vol. 95, pp. 14857–14862, December 1998 Genetics A model system to study genomic imprinting of human genes (Beckwith–Weidemann syndromeygene expressionyimprintingymethylationyPrader–Willi syndrome) J. M. GABRIEL*†,M.J.HIGGINS‡,T.C.GEBUHR*†,T.B.SHOWS‡,S.SAITOH*†§, AND R. D. NICHOLLS*†¶ *Department of Genetics, Case Western Reserve University School of Medicine, and †Center for Human Genetics, University Hospitals of Cleveland, 10900 Euclid Avenue, Cleveland, OH 44106-4955; and ‡Department of Human Genetics, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY 14263 Edited by Francis H. Ruddle, Yale University, New Haven, CT, and approved October 2, 1998 (received for review December 19, 1997) ABSTRACT Somatic-cell hybrids have been shown to main- tumors, is caused both by maternal chromosome 11p15 loss or tain the correct epigenetic chromatin states to study develop- rearrangement and paternal isodisomy (6). Furthermore, muta- mental globin gene expression as well as gene expression on the tions in the imprinted p57KIP2 (CDKN1C) gene have been dis- active and inactive X chromosomes. This suggests the potential covered in some patients with Beckwith–Weidemann syndrome use of somatic-cell hybrids containing either a maternal or a (7), and the maternal (expressed) copy of this gene has been paternal human chromosome as a model system to study known shown to be preferentially deleted in many lung cancers (8) and imprinted genes and to identify as-yet-unknown imprinted genes. down-regulated in Wilms tumors (9, 10). Although the afore- Testing gene expression by using reverse transcription followed mentioned phenotypes are readily discernible, it is likely that by PCR, we show that functional imprints are maintained at four many more genes are subject to genomic imprinting, defects in previously characterized 15q11–q13 loci in hybrids containing a which may lead to more subtle phenotypes.
    [Show full text]
  • Crosstalk Between Mrna 3'-End Processing and Epigenetics
    UC Irvine UC Irvine Previously Published Works Title Crosstalk Between mRNA 3'-End Processing and Epigenetics. Permalink https://escholarship.org/uc/item/13d959vr Authors Soles, Lindsey V Shi, Yongsheng Publication Date 2021 DOI 10.3389/fgene.2021.637705 Peer reviewed eScholarship.org Powered by the California Digital Library University of California MINI REVIEW published: 04 February 2021 doi: 10.3389/fgene.2021.637705 Crosstalk Between mRNA 3'-End Processing and Epigenetics Lindsey V. Soles and Yongsheng Shi * Department of Microbiology and Molecular Genetics, School of Medicine, University of California Irvine, Irvine, CA, United States The majority of eukaryotic genes produce multiple mRNA isoforms by using alternative poly(A) sites in a process called alternative polyadenylation (APA). APA is a dynamic process that is highly regulated in development and in response to extrinsic or intrinsic stimuli. Mis-regulation of APA has been linked to a wide variety of diseases, including cancer, neurological and immunological disorders. Since the first example of APA was described 40 years ago, the regulatory mechanisms of APA have been actively investigated. Conventionally, research in this area has focused primarily on the roles of regulatory cis-elements and trans-acting RNA-binding proteins. Recent studies, however, have revealed important functions for epigenetic mechanisms, including DNA and histone modifications and higher-order chromatin structures, in APA regulation. Here we will discuss these recent findings and their implications
    [Show full text]
  • Gene Imprinting: Engraving the Pathogenesis of Heridetary Diseases
    American Journal of Immunology 10 (1): 14-22, 2014 ISSN: 1553-619X ©2014 Science Publication doi:10.3844/ajisp.2014.14.22 Published Online 10 (1) 2014 (http://www.thescipub.com/aji.toc) GENE IMPRINTING: ENGRAVING THE PATHOGENESIS OF HERIDETARY DISEASES 1Sandeep Satapathy, 2Roshan Kumar Singh and 1Harikrishnan Rajendran 1Departement of Biological Sciences, Indian Institute of Science Education and Research, Bhopal, India 2Departement of Zoology, University of Delhi, New Delhi, India Received 2014-01-11; Revised 2014-01-21; Accepted 2014-02-12 ABSTRACT Gene imprinting has conduited the scope of our understanding of phenotypic expression and its corelation with constituent genotype. It is an epigenetic process that involves DNA methylation and histone modulation to attain monoallelic gene expression without altering the genetic sequences. A distinctive model of non-mendelian genetics, imprinting extends the control over expression of traits and selection of the allele that would direct the same, in a manner decided by the parent of origin. The constitutive existence of this imprinting even after gametogenesis, throughout the somatic development extends a clue for its regulatory hold on several heridetary traits. Several heridetary diseases like Cancers, Russell- Silver syndrome, Beckwith-Wiedemann syndrome, Prader-Willi and Angelman Syndromes and Neurodegenration have shown to be a subsequent error in the genomic impriting process. So, understanding these epigenetic regulations can be a therapeutic strategy for disease modelling and especially targeting their patterns of heridetary inheritance. Keywords: Gene Silencing, Cancers, Neurodegenration, PEGs, MEGs, Heridetary, Russell-Silver Syndrome, Beckwith-Wiedemann Syndrome, Prader-Willi and Angelman Syndromes, Uniparental Disomy (UPD) 1. INTRODUCTION held steady in the stage of fertilization andeven thereafter throughout somatic development ( Fig.
    [Show full text]
  • Gain of Imprinting at Chromosome 11P15: a Pathogenetic Mechanism Identified in Human Hepatocarcinomas
    Gain of imprinting at chromosome 11p15: A pathogenetic mechanism identified in human hepatocarcinomas Christine Schwienbacher*, Laura Gramantieri†, Rosaria Scelfo*, Angelo Veronese*, George A. Calin*, Luigi Bolondi†, Carlo M. Croce‡, Giuseppe Barbanti-Brodano*, and Massimo Negrini*‡§ *Dipartimento di Medicina Sperimentale e Diagnostica, Universita`di Ferrara, via Luigi Borsari 46, 44100 Ferrara, Italy; †Dipartimento di Medicina Interna e Gastroenterologia, Universita`di Bologna, 40100 Bologna, Italy; and ‡Kimmel Cancer Institute, Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA 19107 Contributed by Carlo M. Croce, February 29, 2000 Genomic imprinting is a reversible condition that causes parental- in human tumorigenesis is the detection of loss of imprinting specific silencing of maternally or paternally inherited genes. (LOI) leading to biallelic expression of IGF2 in Wilms’ tumor Analysis of DNA and RNA from 52 human hepatocarcinoma sam- (18, 19). The same abnormality was later detected in BWS (20) ples revealed abnormal imprinting of genes located at chromo- and other neoplasms (21, 22). However, LOI represents a gain some 11p15 in 51% of 37 informative samples. The most frequently of expression of an otherwise imprinted IGF2 allele, a finding detected abnormality was gain of imprinting, which led to loss of that appears to contrast with the notion that loss of maternal expression of genes present on the maternal chromosome. As alleles at chromosome region 11p15 is a crucial event in tumor- compared with matched normal liver tissue, hepatocellular carci- igenesis and BWS. nomas showed extinction or significant reduction of expression of Here, we report that an epigenetic mechanism leading to loss one of the alleles of the CDKN1C, SLC22A1L, and IGF2 genes.
    [Show full text]
  • The Evolution of Genomic Imprinting: Costs, Benefits and Long-Term Consequences
    Biol. Rev. (2014), 89, pp. 568–587. 568 doi: 10.1111/brv.12069 The evolution of genomic imprinting: costs, benefits and long-term consequences Luke Holman∗ and Hanna Kokko Centre of Excellence in Biological Interactions, Division of Ecology, Evolution & Genetics, Research School of Biology, Australian National University, Daley Road, Canberra, Australian Capital Territory 0200, Australia ABSTRACT Genomic imprinting refers to a pattern of gene expression in which a specific parent’s allele is either under-expressed or completely silenced. Imprinting is an evolutionary conundrum because it appears to incur the costs of diploidy (e.g. presenting a larger target than haploidy to mutations) while foregoing its benefits (protection from harmful recessive mutations). Here, we critically evaluate previously proposed evolutionary benefits of imprinting and suggest some additional ones. We discuss whether each benefit is capable of explaining both the origin and maintenance of imprinting, and examine how the different benefits interact. We then outline the many costs of imprinting. Simple models show that circulating deleterious recessives can prevent the initial spread of imprinting, even if imprinting would be evolutionarily stable if it could persist long enough to purge these. We also show that imprinting can raise or lower the mutation load, depending on the selective regime and the degree of dominance. We finish by discussing the population-level consequences of imprinting, which can be both positive and negative. Imprinting offers many insights into evolutionary conflict, the interaction between individual- and population-level fitness effects, and the ‘gene’s-eye view’ of evolution. Key words: evolvability, genetic conflict, mutation load, ploidy, population fitness.
    [Show full text]
  • LECTURE 13: EPIGENETICS – IMPRINTING Reading: Ch. 18, P. 660-664 Problems: Ch. 18, Problems 21-24 Announcements:
    Amacher Lecture 13, 10/19/08 MCB C142/IB C163 LECTURE 13: EPIGENETICS – IMPRINTING Reading: Ch. 18, p. 660-664 Problems: Ch. 18, problems 21-24 Announcements: ** MIDTERM is Thursday, November 6th, from 7-9 pm. It will cover material through Monday, November 3rd. Room assignments will be finalized the week of the exam and posted on the website. No calculators may be used on the exam. Additional information about the midterm and office hours will be posted on the website. ------------------------------------------------------------------------------------------------------------------- In the 1980’s, scientists attempted to create gynogenetic or androgenetic diploids in mammals by putting either two female pronuclei or two male pronuclei into mouse eggs and then transferring the eggs into a foster mother. Control embryos derived from fusion of a maternally-derived pronucleus and a paternally-derived pronucleus developed normally, but embryos from the fusion of two maternally-derived pronuclei or two maternally-derived pronuclei did not develop normally. The only possible genetic difference between males and females in this experiment was the sex chromosomes, but even XX animals failed to thrive! We know now that one of the reasons that mammalian gynogenetic and androgenetic diploids cannot be made is because of an epigenetic phenomenon called genomic imprinting. The expression of an imprinted gene depends upon the parent (maternal or paternal) that transmits it. Epigenetic means “outside the genes”. Epigenetic inheritance describes a variant condition that does not involve a change in DNA sequence, yet is transmitted from one somatic cell generation to the next during development and growth of an organism. Maternal imprinting means that the allele of a particular gene inherited from the mother is transcriptionally silent and the paternally- inherited allele is active.
    [Show full text]