Literature DB >> 18228343

Quantitative fluorescence in situ hybridization (Q-FISH).

Steven S S Poon1, Peter M Lansdorp1.   

Abstract

This unit describes a quantitative technique for measuring the lengths of telomere repeat sequences in individual chromosomes from single metaphase cells. The technique is based on fluorescence in situ hybridization (FISH) adapted for use with peptide nucleic acid (PNA) probes. PNA is an example of novel synthetic oligonucleotide "mimetic" which has a higher affinity than regular oligonucleotide (RNA or DNA) probes for complementary single-strand (ss) DNA sequences. PNA oligonucleotides have excellent penetration properties due to their small size (typically 15 to 18-mers) and can be directly labeled with fluorochromes. These properties have been exploited to develop quantitative fluorescence in situ hybridization (Q-FISH) onto denatured single-stranded chromosomal DNA target sequences. The latter can be present in preparations of fixed metaphase cells on slides (Q-FISH) or in heat-treated (interphase) cells in suspension (flow-FISH).

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Year:  2001        PMID: 18228343     DOI: 10.1002/0471143030.cb1804s12

Source DB:  PubMed          Journal:  Curr Protoc Cell Biol        ISSN: 1934-2616


  25 in total

1.  Probing the mitotic history and developmental stage of hematopoietic cells using single telomere length analysis (STELA).

Authors:  Mark Hills; Kai Lücke; Elizabeth A Chavez; Connie J Eaves; Peter M Lansdorp
Journal:  Blood       Date:  2009-04-09       Impact factor: 22.113

2.  Prolonged self-renewal activity unmasks telomerase control of telomere homeostasis and function of mouse hematopoietic stem cells.

Authors:  Sanja Sekulovic; Vala Gylfadottir; Irma Vulto; Maura Gasparetto; Yasmine Even; Christy Brookes; Clayton Smith; Connie J Eaves; Peter M Lansdorp; Fabio M Rossi; R Keith Humphries
Journal:  Blood       Date:  2011-07-05       Impact factor: 22.113

Review 3.  Early life stress and telomere length: investigating the connection and possible mechanisms: a critical survey of the evidence base, research methodology and basic biology.

Authors:  Idan Shalev
Journal:  Bioessays       Date:  2012-09-19       Impact factor: 4.345

4.  Chromosome orientation fluorescence in situ hybridization to study sister chromatid segregation in vivo.

Authors:  Ester Falconer; Elizabeth Chavez; Alexander Henderson; Peter M Lansdorp
Journal:  Nat Protoc       Date:  2010-07-01       Impact factor: 13.491

5.  Cooperative hybridization of γPNA miniprobes to a repeating sequence motif and application to telomere analysis.

Authors:  Ha H Pham; Connor T Murphy; Gopalsamy Sureshkumar; Danith H Ly; Patricia L Opresko; Bruce A Armitage
Journal:  Org Biomol Chem       Date:  2014-10-07       Impact factor: 3.876

6.  Observation and Quantification of Telomere and Repetitive Sequences Using Fluorescence In Situ Hybridization (FISH) with PNA Probes in Caenorhabditis elegans.

Authors:  Beomseok Seo; Junho Lee
Journal:  J Vis Exp       Date:  2016-08-04       Impact factor: 1.355

7.  Zscan4 Inhibits Maintenance DNA Methylation to Facilitate Telomere Elongation in Mouse Embryonic Stem Cells.

Authors:  Jiameng Dan; Philippe Rousseau; Swanand Hardikar; Nicolas Veland; Jiemin Wong; Chantal Autexier; Taiping Chen
Journal:  Cell Rep       Date:  2017-08-22       Impact factor: 9.423

8.  The Werner syndrome protein suppresses telomeric instability caused by chromium (VI) induced DNA replication stress.

Authors:  Fu-Jun Liu; Aaron Barchowsky; Patricia L Opresko
Journal:  PLoS One       Date:  2010-06-16       Impact factor: 3.240

9.  Human RAP1 inhibits non-homologous end joining at telomeres.

Authors:  Jay Sarthy; Nancy S Bae; Jonathan Scrafford; Peter Baumann
Journal:  EMBO J       Date:  2009-09-17       Impact factor: 11.598

10.  Rapid analysis of chromosome aberrations in mouse B lymphocytes by PNA-FISH.

Authors:  Sarah M Misenko; Samuel F Bunting
Journal:  J Vis Exp       Date:  2014-08-19       Impact factor: 1.355

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