Variation in restriction fragment length and methylation pattern of rat major histocompatibility complex class I genes

A. G. Uitterlinden, Jan Vijg, D. L. Knook

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

To investigate the methylation state of MHC class I sequences, genomic DNAs were digested in parallel with the restriction enzymes MspI and HpaII and subsequently analyzed by Southern blot hybridization. MspI and HpaII both recognize the sequence 5'-CCGG-3', but HpaII will not cut this sequence when the internal cytosine residue is methylated. When DNAs, isolated from the liver and spleen of WAG rats, were compared in this way, differences in the methylation patterns of these two organs were found. The data on the arrangement and methylation state of rat MHC class I sequences imply: haplotype-specific restriction fragment-length polymorphisms and methylation patterns; variation in MHC methylation pattern between organs; and a demethylated state of MHC sequences in tumors. These findings can be considered as a first step to a more complete direct examination of MHC methylation patterns in different tissues of aging rats. Such a study seems relevant in view of the suggestion that the function of DNA methylation in vertebrates is somehow related to the control of gene expression.

Original languageEnglish (US)
Pages (from-to)1805-1807
Number of pages3
JournalTransplantation Proceedings
Volume17
Issue number3
StatePublished - 1985
Externally publishedYes

Fingerprint

MHC Class I Genes
Major Histocompatibility Complex
Methylation
Cytosine
DNA Methylation
Southern Blotting
Restriction Fragment Length Polymorphisms
Haplotypes
Vertebrates
Spleen
Gene Expression
Liver
DNA
Enzymes
Neoplasms

ASJC Scopus subject areas

  • Surgery
  • Transplantation

Cite this

Variation in restriction fragment length and methylation pattern of rat major histocompatibility complex class I genes. / Uitterlinden, A. G.; Vijg, Jan; Knook, D. L.

In: Transplantation Proceedings, Vol. 17, No. 3, 1985, p. 1805-1807.

Research output: Contribution to journalArticle

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