Literature DB >> 1764989

Methylation levels of maternal and paternal genomes during preimplantation development.

S K Howlett1, W Reik.   

Abstract

The methylation status of three highly repeated sequences was studied in sperm, eggs and preimplantation embryos with different combinations of parental chromosomes. High levels of methylation of the IAP and MUP sequence families were found in sperm and in eggs, whereas the L1 repeat was found to be highly methylated in sperm but only about 42% methylated in eggs. To assess how the two parental genomes behaved during preimplantation development, normal, fertilised embryos were compared with parthenogenetic embryos where the chromosomes are exclusively of maternal origin. It was observed that the high levels of methylation at the IAP and MUP sequences were retained through early development, with the first signs of demethylation at the IAP sequences apparent on both parental chromosomes in the blastocyst. Methylation at the sperm-derived L1 sequences dropped to about the same level as that of the egg-derived sequences by the late 2-cell stage, both then remain at this intermediate level until around the time of cavitation when levels fell to about 10% in the blastocyst. High levels of DNA methylase were detected in germinal vesicle and metaphase II oocytes; these high levels were maintained in fertilised and parthenogenetic embryos through into the morula and then declined to be undetectable in the blastocyst. Our comparison of maternal and paternal genomes suggests that methylation levels at repeat sequences are remarkably similar at the time of fertilisation or, as in the case of the L1 sequences, they become so during the first few cell cycles. Hence, there do not appear to be global methylation differences between the genomes that are retained through preimplantation development.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1991        PMID: 1764989     DOI: 10.1242/dev.113.1.119

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  72 in total

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2.  Novel methylation at GpC dinucleotide in the fish Sparus aurata genome.

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4.  5-Methylcytosine DNA glycosylase participates in the genome-wide loss of DNA methylation occurring during mouse myoblast differentiation.

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6.  Epigenetics and assisted reproductive technology: a call for investigation.

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Review 8.  High-throughput sequencing offers new insights into 5-hydroxymethylcytosine.

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9.  Multiple genes exhibit phenobarbital-induced constitutive active/androstane receptor-mediated DNA methylation changes during liver tumorigenesis and in liver tumors.

Authors:  Jennifer M Phillips; Jay I Goodman
Journal:  Toxicol Sci       Date:  2009-02-20       Impact factor: 4.849

10.  Alcohol exposure alters DNA methylation profiles in mouse embryos at early neurulation.

Authors:  Yunlong Liu; Yokesh Balaraman; Guohua Wang; Kenneth P Nephew; Feng C Zhou
Journal:  Epigenetics       Date:  2009-10-01       Impact factor: 4.528

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