Literature DB >> 2824285

Human muscle carbonic anhydrase: gene structure and DNA methylation patterns in fetal and adult tissues.

J Lloyd1, C Brownson, S Tweedie, J Charlton, Y H Edwards.   

Abstract

We report the isolation and analysis of genomic clones comprising the entire gene coding for the human muscle carbonic anhydrase, CAIII. The gene spans 10.3 kb and has a seven-exon/six-intron structure. A noncanonical TATA box, a CCAAT motif, and two CCGCCC elements are present in the sequences upstream of exon 1. Although the expression of CAIII shows strict tissue specificity, the gene exhibits a number of features normally associated with housekeeping enzymes. For example, there is 48% homology with a 25-bp consensus sequence between the TATA box and the cap site and there is a CpG-rich island spanning a 469-bp sequence near to the origin of transcription. Methylation studies suggest that some CCGG sites clustered in the CpG-rich island are undermethylated in DNA from fetal and adult muscle and in other tissues irrespective of CAIII expression. In contrast, several nonclustered CCGG sites show a methylation pattern that correlates with gene expression. However DNA from differentiated type II adult muscle fibers is undermethylated at these sites even though CAIII is not expressed.

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Year:  1987        PMID: 2824285     DOI: 10.1101/gad.1.6.594

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  5 in total

1.  The mouse carbonic anhydrase I gene contains two tissue-specific promoters.

Authors:  P Fraser; P Cummings; P Curtis
Journal:  Mol Cell Biol       Date:  1989-08       Impact factor: 4.272

2.  Structure of the carbonic anhydrase VI (CA6) gene: evidence for two distinct groups within the alpha-CA gene family.

Authors:  W Jiang; D Gupta
Journal:  Biochem J       Date:  1999-12-01       Impact factor: 3.857

3.  Structure and differential expression of two genes encoding carbonic anhydrase in Chlamydomonas reinhardtii.

Authors:  S Fujiwara; H Fukuzawa; A Tachiki; S Miyachi
Journal:  Proc Natl Acad Sci U S A       Date:  1990-12       Impact factor: 11.205

4.  Carbonic anhydrase II deficiency syndrome in a Belgian family is caused by a point mutation at an invariant histidine residue (107 His----Tyr): complete structure of the normal human CA II gene.

Authors:  P J Venta; R J Welty; T M Johnson; W S Sly; R E Tashian
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

5.  Mouse carbonic anhydrase III: nucleotide sequence and expression studies.

Authors:  S Tweedie; Y Edwards
Journal:  Biochem Genet       Date:  1989-02       Impact factor: 1.890

  5 in total

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