Literature DB >> 487434

Methylated and unmethylated DNA compartments in the sea urchin genome.

A P Bird, M H Taggart, B A Smith.   

Abstract

Sea urchin (Echinus esculentus) DNA has been separated into high and low molecular weight fractions by digestion with the mCpG-sensitive restriction endonucleases Hpa II, Hha I and Ava I. The separation was due to differences in methylation at the recognition sequences for these enzymes because an mCpG-insensitive isoschizomer of Hpa II (Msp I) digested Hpa II-resistant DNA to low molecular weight, showing that many Hpa II sites were in fact present in this fraction; and because 3H-methyl methionine administered to embryos was incorporated into the high molecular weight Hpa II-, Hha I- and Ava I-resistant fraction, but not significantly into the low molecular weight fraction. The fraction resistant to Hpa II, Hha I and Ava I amounted to about 40% of the total DNA. It consisted of long sequence tracts between 15 and well over 50 kg in length, in which many sites for each of these enzymes were methylated consecutively. The remaining 60% of the genome, (m-), was not significantly methylated. Methylated and unmethylated fractions were considered to be subfractions of the genome because enriched unique sequences from one fraction cross-reassociated poorly with the other fraction and specific sequences were found in either (m+) or (m-) but not in both (see below). Similar (m+) and (m-) compartments were found in embryos, germ cells and adult somatic tissues. Furthermor, we found no evidence for changes in the sequence composition of (m+) or (m-) between sperm, embryo or intestine DNAs, although low levels of exchange would not have been detected. Using cloned Echinus histone DNA, heterologous 5S DNA and ribosomal DNA probes, we have found that each of these gene families belongs to the unmethylated DNA compartment in all the tissues examined. In particular, there was no detectable methylation of histone DNA either in early embryos, which are thought to be actively transcribing the bulk of histone genes, or in sperm and gastrulae, in which most histone genes are not being transcribed. In contrast to these gene families, sequences complementary to an internally repetitious Echinus DNA clone were found primarily in the methylated DNA compartment.

Entities:  

Mesh:

Substances:

Year:  1979        PMID: 487434     DOI: 10.1016/0092-8674(79)90329-5

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  69 in total

1.  Phenotypic switching in cells transformed with the herpes simplex virus thymidine kinase gene.

Authors:  M Ostrander; S Vogel; S Silverstein
Journal:  Mol Cell Biol       Date:  1982-06       Impact factor: 4.272

2.  Cleavage of methylated CCCGGG sequences containing either N4-methylcytosine or 5-methylcytosine with MspI, HpaII, SmaI, XmaI and Cfr9I restriction endonucleases.

Authors:  V Butkus; L Petrauskiene; Z Maneliene; S Klimasauskas; V Laucys; A Janulaitis
Journal:  Nucleic Acids Res       Date:  1987-09-11       Impact factor: 16.971

3.  DNA methylation pattern changes during development of a sea urchin.

Authors:  J Fronk; G A Tank; J P Langmore
Journal:  Biochem J       Date:  1992-05-01       Impact factor: 3.857

4.  CpG methylation is targeted to transcription units in an invertebrate genome.

Authors:  Miho M Suzuki; Alastair R W Kerr; Dina De Sousa; Adrian Bird
Journal:  Genome Res       Date:  2007-04-09       Impact factor: 9.043

Review 5.  Biological aspects of cytosine methylation in eukaryotic cells.

Authors:  M Hergersberg
Journal:  Experientia       Date:  1991-12-01

6.  Ribosomal DNA methylation in a flax genotroph and a crown gall tumour.

Authors:  K S Blundy; C A Cullis; A G Hepburn
Journal:  Plant Mol Biol       Date:  1987-05       Impact factor: 4.076

Review 7.  CpG islands and the regulation of transcription.

Authors:  Aimée M Deaton; Adrian Bird
Journal:  Genes Dev       Date:  2011-05-15       Impact factor: 11.361

8.  Methylation of genomes and genes at the invertebrate-vertebrate boundary.

Authors:  S Tweedie; J Charlton; V Clark; A Bird
Journal:  Mol Cell Biol       Date:  1997-03       Impact factor: 4.272

9.  Effect of site-specific methylation on DNA modification methyltransferases and restriction endonucleases.

Authors:  M Nelson; M McClelland
Journal:  Nucleic Acids Res       Date:  1989       Impact factor: 16.971

10.  Structure of the sea urchin U1 RNA repeat.

Authors:  D T Brown; G F Morris; N Chodchoy; C Sprecher; W F Marzluff
Journal:  Nucleic Acids Res       Date:  1985-01-25       Impact factor: 16.971

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.