Literature DB >> 8213817

Hereditary overexpression of adenosine deaminase in erythrocytes: evidence for a cis-acting mutation.

E H Chen1, A P Tartaglia, B S Mitchell.   

Abstract

Overexpression of adenosine deaminase (ADA) in red blood cells is inherited as an autosomal dominant trait and causes hemolytic anemia. The increased ADA activity in erythrocytes is due to an increase in steady-state levels of ADA mRNA of normal sequence. Increased ADA mRNA may be due to a cis-acting mutation which results in increased transcription or a loss of down-regulation during erythroid differentiation. Alternatively, it is possible that the mutation is in a trans-acting factor which interacts with normal ADA transcriptional elements to cause overexpression in red blood cells. To discriminate between a cis-acting and a trans-acting mutation, we took advantage of a highly polymorphic TAAA repeat located at the tail end of an Alu repeat approximately 1.1 kb upstream of the ADA gene. Using PCR to amplify this region, we identified five different alleles in 19 members of the family. All 11 affected individuals had an ADA allele with 12 TAAA repeats, whereas none of the 8 normal individuals did. We conclude that this disorder results from a cis-acting mutation in the vicinity of the ADA gene.

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Year:  1993        PMID: 8213817      PMCID: PMC1682400     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  21 in total

1.  A single point mutation is the cause of the Greek form of hereditary persistence of fetal haemoglobin.

Authors:  M Berry; F Grosveld; N Dillon
Journal:  Nature       Date:  1992-08-06       Impact factor: 49.962

2.  A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.

Authors:  M M Bradford
Journal:  Anal Biochem       Date:  1976-05-07       Impact factor: 3.365

3.  Cell type-specific transcriptional regulation of the human adenosine deaminase gene.

Authors:  D L Lattier; J C States; J J Hutton; D A Wiginton
Journal:  Nucleic Acids Res       Date:  1989-02-11       Impact factor: 16.971

4.  Elevated erythrocyte adenosine deaminase activity in a patient with primary acquired sideroblastic anemia.

Authors:  H Kanno; H Fujii; K Tani; T Morisaki; K Takahashi; N Horiuchi; M Kizaki; T Ogawa; S Miwa
Journal:  Am J Hematol       Date:  1988-03       Impact factor: 10.047

5.  A case of red-cell adenosine deaminase overproduction associated with hereditary hemolytic anemia found in Japan.

Authors:  S Miwa; H Fujii; N Matsumoto; T Nakatsuji; S Oda; H Asano; S Asano
Journal:  Am J Hematol       Date:  1978       Impact factor: 10.047

6.  Easy calculations of lod scores and genetic risks on small computers.

Authors:  G M Lathrop; J M Lalouel
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

7.  Elevated adenosine deaminase activity and hereditary hemolytic anemia. Evidence for abnormal translational control of protein synthesis.

Authors:  E G Chottiner; H J Cloft; A P Tartaglia; B S Mitchell
Journal:  J Clin Invest       Date:  1987-03       Impact factor: 14.808

8.  Elevated erythrocyte adenosine deaminase activity in patients with acquired immunodeficiency syndrome.

Authors:  M J Cowan; R O Brady; K J Widder
Journal:  Proc Natl Acad Sci U S A       Date:  1986-02       Impact factor: 11.205

9.  Biochemical study of a case of hemolytic anemia with increased (85 fold) red cell adenosine deaminase.

Authors:  J L Pérignon; M Hamet; H A Buc; P H Cartier; M Derycke
Journal:  Clin Chim Acta       Date:  1982-09-15       Impact factor: 3.786

10.  Elevated erythrocyte adenosine deaminase activity in congenital hypoplastic anemia.

Authors:  B E Glader; K Backer; L K Diamond
Journal:  N Engl J Med       Date:  1983-12-15       Impact factor: 91.245

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