Article Data

  • Views 237
  • Dowloads 128

Reviews

Open Access

Evaluation of DNA methylation in the human genome: Why examine it and what method to use

  • J.P. Geisler1,*,
  • K. J. Manahan1
  • H. E. Geisler2

1Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA

2Division of Gynecologic Oncology, St. Vincent Hospitals, Indianapolis, Indiana, USA

DOI: 10.12892/ejgo20040119 Vol.25,Issue 1,January 2004 pp.19-24

Published: 10 January 2004

*Corresponding Author(s): J.P. Geisler E-mail:

Abstract

Purpose: Since its discovery 50 years ago, DNA methylation has been found to be an important part of gene regulation. Newer methods of analysis over the last decade have helped further the understanding of this epigenetic phenomenon. The purpose of this article is to describe current methods of analysis and discuss advantages and disadvantages of each and their possible roles in gynecologic malignancies.

Results: The methods for analysis of DNA methylation are divided into two major categories: 1) methods which utilize chemical methods or restriction enzymes to differentially cleave at cytosine versus 5-methylcytosine sites, 2) methods which utilize sodium bisulfite (NaHSO3) to specifically convert unmethylated cytosines to uracil (thymine after PCR). This recently developed method appears to be more sensitive and allows the investigator to specifically delineate the study site(s).

Conclusion: DNA methylation is important in the human genome. Its role in tumorigenesis is just beginning to be understood. While relying upon newly designed methods of analysis, further understanding of this epigenetic phenomenon and its role in gene expression and tumorigenesis will be forthcoming.

Keywords

Methylation; Tumor suppressor genes; CpG; Mutation

Cite and Share

J.P. Geisler,K. J. Manahan,H. E. Geisler. Evaluation of DNA methylation in the human genome: Why examine it and what method to use. European Journal of Gynaecological Oncology. 2004. 25(1);19-24.

References

[1] Hotchkiss R. D. J. Biol. Chem., 1948, 168, 315.

[2] Clark S. J., Harrison J., Paul C. L.: "Frommer M. High sensitivity mapping of methylated cytosines". Nuc. Acid. Res., 1994, 22, 2990.

[3] Ehrlich M., Gama-Sosa M. A., Huang L. H., Midgett R. M., Kuo K. C., McCune R. A., Gehrke C.: "Amount and distribution of 5-methylcytosine in human DNA from different types of cells". Nucleic Acids Res., 1982, 10, 2709.

[4] Momparler R. L., Bovenzi V.: ·'DNA methylation and cancer". J. Cell. Physiol., 2000, 183, 145.

[5] Neumann B., Barlow D. P.: "Multiple roles for DNA methylation in gametic imprinting". Curr. Opin. Genet. Develop., 1996, 6, 159.

[6] Barlow D. P.: "Gametic imprinting in mammals". Science, 1995, 270, 1610.

[7] Robertson K. D., Jones P. A.: "DNA methylation: past, present and future directions". Carcinogenesis, 2000, 21, 461.

[8] Kubota T.,N onoyama S.,To noki H.,M asumo M.,I maizumi Kojima M.,W akui K. et al.: "A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCR". Hum. Genet, 1999, 104, 49.

[9] Toyota M., Issa J.P. J.:'The role of DNA hypermethylation in human neoplasia". Electrophoresis, 2000, 21, 329.

[10] Rideout W. M. I., Coetzee G. A., Olumi A. F., Jones P. A.: "5-Methylcytosine as an endogenousmutagen in the human LDL receptor and p53 genes". Science, 1990, 249, 1288.

[11] Mathur P., Xu J., Dedon P. C.: "Cytosine methylation enhances DNA damage produced by groove binding and intercalatmg enediynes: studies with experamicins Al and C". Biochemistry, 1997, 36, 14868.

[12] Lou W.,K rill D.,D hir R.,B ecich M. J.,D ong J. T.,F rierson H.F. et al.: "Methylation of the CD44 metastasis suppressor gene in human prostate cancer". Cancer Res., 1999, 59, 2329.

[13] Tang x, Khun F R, Lee J J. Kemp B L, Lm D, Hong W k, Mao L “Hypermethylauon of death-assocmted protem (DAP) kinase promoter and aggressiveness in stage I non-small-cell lung cancer". J. Natl. Cancer Inst., 200, 92, 1511.

[14] Domann F. E., Rice J. C., Hendrix M. J. C., Futscher B. W.: "Epigenetic silencing of maspin gene expression in juman breast cancers". Int. J. Cancer, 2000, 85, 805.

[15] Baylin S. B., Herman J. G., Graff J. R., Vertino P. M., Issa J.P.: "Alterations in DNA methylation: a fundamental aspect of neoplasia". Adv Cancer Res., 1998, 72, 141.

[16] Kersting M.,F riedl C., Kraus A., Behn M., Pankow W., Schuerman M.: "Differentialfrequencies of p16'""" promoter hypermethylation, p53 mutation, and K-ras mutation in exfoliative material mark the development of lung cancer on symptomatic chronic smokers". J. Clin. Oncol., 2000, 18, 3221.

[17] Saluz H.. Jost J.P.: "A simple high-resolution procedure to study DNA methylation an in vivo DBA-protien interaction on a singlecopy gene level in higher eukaryotes". Proc. Natl. Acad. Sciences, 1989, 86, 2602.

[18] Thomassin H., Oakeley E. J., Grange T.: "Identification of 5-methylcytosine in complex genomes". Methods, 1999, 19, 465.

[19] Herman J. G., Graff J., Myohanen S., Nelkin B. D., Baylin S. B.: "Methylation-specific PCR: a novel PCR assay for methylation status of CpG islands". Proc. Natl. Acad. Sci. USA, 1996, 93, 9821.

[20] Tremblay K. D., Saam J. R., Ingram R. S., Tilgham S. M., Bartolomei M. S.: "A paternal-specific methylation imprint marks the alleles of the mouse H19 gene". Nat. Genetics, 1995, 9, 407.

[21] Stoger R., Kubicka P., Liu C. G., Kafri T., Razin A., Cedar H., Barlow D. P.: "Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal". Cell, 1993, 73, 1827.

[221 Aggerholm A., Hokland P., Guldberg P.: "DAP-kinase CpG island methylation in acute myeloid leukemia: methodology vs. biology?". Blood, 2000, 95, 2997.

[23] Zhang X., Huang C. J., Nazarian R., Ritchie T., de Vellis J. S., Noble E. P.: "Use of a single sequencing termination reaction to distinguish between cytosine and 5-methylcytosine in bisulfite-modified DNA". Biotechniques, 1997, 22, 850.

[24] Aggerholm A., Guldberg P., Hokland M., Hokland P.: "Extensive intr- and interindividual heterogeneity of p15INK4B methylation in acute myeloid leukemia". Cancer Res.. 1999, 59, 436.

[25] Katzenellenbogen R. A., Baylin S. B., Herman J. G.: " Hypermethylation of the DAP-kinase CpG island is a common alteration in B-cell malignancies". Blood, I 999, 93, 4347.

[26] Herman J. G.: "DAP-kinase methylation: methodology and biology". Blood, 2000, 95, 2998.

[27] Boyes J., Bird A.: "Repression of genes by DNA methylation depends on CpG density and promoter strenght: evidense for involvement of methyl-CpG binding". EMBO J., 1992, 11, 327.

[28] Herman J. G., Umar A., Polyak K.. Graff J. R., Ahuja N., Issa J.P. J. et al.: "Incidence and functional consequences of hMLHI promoter hypermethylation in colorectal carcinoma". Proc. Natl. Acad. Sci. USA, 1998, 95, 6870.

[29] Yanagisawa Y.,A kiyama Y.,I ida S.,I to E.,N omizu T.,S ugihara K. et al.: "Methylation of the hMLHI promoter in familial gastric cancer with microsatellite instability". Int. J. Cancer, 2000, 85, 50.

[30] Esteller M., Silva J. M., Dominguez G., Bonilla F., Matias-Guiu X., Lerma E. et al.: "Promoter hypermethylation and BRCA I inactivation and sporadic breast and ovarian tumors".J. Natl. Cancer Inst., 2000, 92, 564.

[31] Geisler J. P., Ratterman-Zogg M. A., Rathe J. A., Buller R. E.: "BRCAI dysfunction is common in ovarian cancer". J. Natl. Cancer Inst., 2002, 94, 61.

[32] Hilton J. L., Geisler J.P.. Rathe J. A., Hattermann-Zogg M. A., De Young B., Buller R. E.: "Inactivation of BRCAI and BRCA2 in ovarian cancer". J. Natl. Cancer Inst., 2002, 94. 1396.

[33] Geisler J.P., Sood A. L., Holmes R. J., Ratterman-Zogg M. A., Rathe J. A., Buller R. E.: "Mismatch repair gene expression defects contribute to microsatellite instability in ovarian cancer". Cancer (in press), 2003.

[34] Baylin S. B., Herman J. G.: "DNA hypermethylation in tumorigenesis: epigenetics joins genetics". Trends Genet., 2000, 16, 168.

[35] Newell-Price J., Clark A. J. L.. King P.: "DNA methylation and silencing of gene expression". Trends Enducrinol. Metabol., 2000. ll, 142.

[36] Fleisher A. S.,E steller M.,W ang S.,T amura G.,S uzuki H.,Y in J. et al.:" Hypermethylation of the hMLHI gene promoter mJuman gastric cancers with microsatellite instability". Cancer Res., 1999, 59, 1090.

Abstracted / indexed in

Science Citation Index Expanded (SciSearch) Created as SCI in 1964, Science Citation Index Expanded now indexes over 9,500 of the world’s most impactful journals across 178 scientific disciplines. More than 53 million records and 1.18 billion cited references date back from 1900 to present.

Biological Abstracts Easily discover critical journal coverage of the life sciences with Biological Abstracts, produced by the Web of Science Group, with topics ranging from botany to microbiology to pharmacology. Including BIOSIS indexing and MeSH terms, specialized indexing in Biological Abstracts helps you to discover more accurate, context-sensitive results.

Google Scholar Google Scholar is a freely accessible web search engine that indexes the full text or metadata of scholarly literature across an array of publishing formats and disciplines.

JournalSeek Genamics JournalSeek is the largest completely categorized database of freely available journal information available on the internet. The database presently contains 39226 titles. Journal information includes the description (aims and scope), journal abbreviation, journal homepage link, subject category and ISSN.

Current Contents - Clinical Medicine Current Contents - Clinical Medicine provides easy access to complete tables of contents, abstracts, bibliographic information and all other significant items in recently published issues from over 1,000 leading journals in clinical medicine.

BIOSIS Previews BIOSIS Previews is an English-language, bibliographic database service, with abstracts and citation indexing. It is part of Clarivate Analytics Web of Science suite. BIOSIS Previews indexes data from 1926 to the present.

Journal Citation Reports/Science Edition Journal Citation Reports/Science Edition aims to evaluate a journal’s value from multiple perspectives including the journal impact factor, descriptive data about a journal’s open access content as well as contributing authors, and provide readers a transparent and publisher-neutral data & statistics information about the journal.

Submission Turnaround Time

Conferences

Top