Literature DB >> 6559636

Hybridization histochemistry: use of recombinant DNA for tissue localizations of specific mRNA populations.

J P Coghlan, J D Penschow, P J Hudson, H D Niall.   

Abstract

A procedure of in situ hybridization, termed hybridization histochemistry has been developed to locate in specially prepared whole sections of tissue those areas which contain specific mRNA populations, the presence of which would indicate that a certain gene is "switched on" and production of a specific protein or peptide is highly probable. In the main 32P-labelled recombinant DNA probes were used. These probes were complementary to several peptide hormones or enzymes. 32P-labelled DNA probes were favoured initially because the short time needed for exposure enabled the development of the procedure to proceed quickly. The results indicate that the mRNA's of the species being examined are present in whole sections of tissue in a physical state which leaves them accessible to cDNA probes. The results are highly reproducible and specific. Because the method allows a clear distinction to be made between those cells which manufacture a peptide or protein and those which have imported the material it will have a special use in resolving many controversies over specific sites of origin of peptides and proteins, especially in tissues e.g. CNS and gut which are functionally complex and morphologically heterogeneous.

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Year:  1984        PMID: 6559636     DOI: 10.3109/10641968409062551

Source DB:  PubMed          Journal:  Clin Exp Hypertens A        ISSN: 0730-0077


  11 in total

1.  Detection of mRNA and hnRNA using a digoxigenin labelled cDNA probe by in situ hybridization on frozen tissue sections.

Authors:  N Maggiano; L M Larocca; M Piantelli; F O Ranelletti; L Lauriola; R Ricci; A Capelli
Journal:  Histochem J       Date:  1991-02

2.  Ultrastructural detection of the vasopressin messenger RNA in the normal and Brattleboro rat.

Authors:  A F Guitteny; B Bloch
Journal:  Histochemistry       Date:  1989

3.  Localisation of immunoreactive kininogen and tissue kallikrein in the human nephron.

Authors:  C D Figueroa; A G MacIver; J C Mackenzie; K D Bhoola
Journal:  Histochemistry       Date:  1988

Review 4.  Hybridization histochemistry.

Authors:  J D Penschow; J Haralambidis; P E Darling; I A Darby; E M Wintour; G W Tregear; J P Coghlan
Journal:  Experientia       Date:  1987-07-15

5.  Activation of the human beta-interferon gene requires an interferon-inducible factor.

Authors:  T Enoch; K Zinn; T Maniatis
Journal:  Mol Cell Biol       Date:  1986-03       Impact factor: 4.272

6.  In situ hybridization using 32P labelled oligodeoxyribonucleotides for the cellular localisation of mRNA in neuronal and endocrine tissue. An analysis of procedural variables.

Authors:  J V Priestley; M A Hynes; V K Han; M Réthelyi; E R Perl; P K Lund
Journal:  Histochemistry       Date:  1988

Review 7.  Biochemistry and pharmacology of the renin-angiotensin system.

Authors:  C I Johnston
Journal:  Drugs       Date:  1990       Impact factor: 9.546

Review 8.  Gut endocrine and neural peptides.

Authors:  Anne E Bishop; Julia M Polak
Journal:  Endocr Pathol       Date:  1990-03       Impact factor: 3.943

9.  Visualisation of messenger RNA directing peptide synthesis by in situ hybridisation using a novel single-stranded cDNA probe. Potential for the investigation of gene expression and endocrine cell activity.

Authors:  I M Varndell; J M Polak; K L Sikri; C D Minth; S R Bloom; J E Dixon
Journal:  Histochemistry       Date:  1984

10.  Localization of atrial natriuretic peptide mRNA and immunoreactivity in the rat heart and human atrial appendage.

Authors:  Q Hamid; J Wharton; G Terenghi; C J Hassall; J Aimi; K M Taylor; H Nakazato; J E Dixon; G Burnstock; J M Polak
Journal:  Proc Natl Acad Sci U S A       Date:  1987-10       Impact factor: 11.205

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