Literature DB >> 6863020

Studies of X-chromosome inactivation with an improved histochemical technique for ornithine carbamoyltransferase.

K A Wareham, S Howell, D Williams, E D Williams.   

Abstract

Studies of X-linked enzymes provide an approach to the study of tumour and normal cellular development. We have assessed the technique for the histochemical demonstration of one such enzyme, ornithine carbamoyltransferase (EC 2.1.3.3). Various stages in the Mizutani technique for ornithine carbamoyltransferase were re-examined, and the resulting improved technique applied to normal mice and to mice of the sparse fur strain (Spf) known to have an abnormal form of ornithine carbamoyltransferase inherited as an X-linked characteristic. Positive enzyme activity was present in all hepatocytes from normal mice, the strongest reaction being present in the periportal area with a gradual reduction of activity towards the centrilobular region. No activity was demonstrable in hepatocytes from hemizygous male Spf mice. In heterozygous female Spf mice, there was a clear-cut separation of ornithine carbamoyl-transferase-positive and -negative cells. These were present in very variable proportions in different liver lobes and different animals. Preliminary studies were also carried out using a high pH reaction mixture to detect the abnormal enzyme. These studies demonstrate conclusively the X-linkage of ornithine carbamoyltransferase in mice, showing the mosaic pattern of distribution predicted by the Lyon hypothesis. They show that the Spf strain of mice can be used for studies of both development and tumorigenesis in the liver, and that histochemical study of an animal strain with an X-linked enzyme abnormality provides a powerful investigative tool.

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Year:  1983        PMID: 6863020     DOI: 10.1007/bf01002969

Source DB:  PubMed          Journal:  Histochem J        ISSN: 0018-2214


  17 in total

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Authors:  A B NOVIKOFF; E ESSNER
Journal:  Am J Med       Date:  1960-07       Impact factor: 4.965

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Authors:  P J Fialkow
Journal:  Biochim Biophys Acta       Date:  1976-10-12

3.  X-chromosome inactivation in human liver: confirmation of X-linkage of ornithine transcarbamylase.

Authors:  F C Ricciuti; T D Gelehrter; L E Rosenberg
Journal:  Am J Hum Genet       Date:  1976-07       Impact factor: 11.025

4.  Abnormal ornithine carbamoyltransferase in mice having the sparse-fur mutation.

Authors:  R DeMars; S L LeVan; B L Trend; L B Russell
Journal:  Proc Natl Acad Sci U S A       Date:  1976-05       Impact factor: 11.205

Review 5.  The origin and development of human tumors studied with cell markers.

Authors:  P J Fialkow
Journal:  N Engl J Med       Date:  1974-07-04       Impact factor: 91.245

Review 6.  X-chromosome inactivation and developmental patterns in mammals.

Authors:  M F Lyon
Journal:  Biol Rev Camb Philos Soc       Date:  1972-01

Review 7.  Gene control of mammalian differentiation.

Authors:  B Mintz
Journal:  Annu Rev Genet       Date:  1974       Impact factor: 16.830

8.  X-linked transmission of ornithine-transcarbamylase deficiency.

Authors:  C R Scott; C C Teng; S I Goodman; A Greensher; J W Mace
Journal:  Lancet       Date:  1972-11-25       Impact factor: 79.321

9.  Cytochemical demonstration of ornithine carbamoyltransferase activity in liver mitochondria of rat and mouse.

Authors:  A Mizutani
Journal:  J Histochem Cytochem       Date:  1968-03       Impact factor: 2.479

10.  Ornithine transcarbamylase deficiency: a cause of lethal neonatal hyperammonemia in males.

Authors:  A G Campbell; L E Rosenberg; P J Snodgrass; C T Nuzum
Journal:  N Engl J Med       Date:  1973-01-04       Impact factor: 91.245

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  6 in total

Review 1.  Ornithine carbamoyl transferase deficiency: findings, models and problems.

Authors:  C Bachmann
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

2.  Differential methylation of the ornithine carbamoyl transferase gene on active and inactive mouse X chromosomes.

Authors:  L J Mullins; G Veres; C T Caskey; V Chapman
Journal:  Mol Cell Biol       Date:  1987-11       Impact factor: 4.272

Review 3.  The role of histochemical investigations in metabolic disorders affecting the liver.

Authors:  B D Lake
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

4.  In vivo nitrogen metabolism in ornithine transcarbamylase deficiency.

Authors:  M Yudkoff; Y Daikhin; I Nissim; A Jawad; J Wilson; M Batshaw
Journal:  J Clin Invest       Date:  1996-11-01       Impact factor: 14.808

5.  In vivo measurement of ureagenesis with stable isotopes.

Authors:  M Yudkoff; Y Daikhin; X Ye; J M Wilson; M L Batshaw
Journal:  J Inherit Metab Dis       Date:  1998       Impact factor: 4.982

6.  Clonal origin of mouse liver cell tumors.

Authors:  S Howell; K A Wareham; E D Williams
Journal:  Am J Pathol       Date:  1985-12       Impact factor: 4.307

  6 in total

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