Literature DB >> 17697125

Perichromatin fibrils as early markers of transcriptional alterations.

Marco Biggiogera1, Barbara Cisterna, Alessandro Spedito, Lorella Vecchio, Manuela Malatesta.   

Abstract

Perichromatin fibrils represent the morphological expression of transcription and co-transcriptional processing of pre-mRNA. They can be considered, hence, an example of work in progress. High resolution techniques such as electron microscopy demonstrate that perichromatin fibrils play a role as early markers of transcriptional alterations. In this paper, we review some experimental and physiological conditions impairing or modulating transcription as well as their effects on perichromatin fibrils. In all the situations reported, perichromatin fibrils show modifications in their amount and/or their associated proteins. Their movements are also affected, as well as their export or their intra-nuclear storage forms. Perichromatin fibrils therefore represent highly sensitive markers not only for monitoring transcriptional and processing rate but also for identifying the maturation level of pre-mRNA/mRNA occurring in the cell nucleus and the functional correlation with the cellular metabolic state.

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Year:  2007        PMID: 17697125     DOI: 10.1111/j.1432-0436.2007.00211.x

Source DB:  PubMed          Journal:  Differentiation        ISSN: 0301-4681            Impact factor:   3.880


  17 in total

1.  New centromeric component CENP-W is an RNA-associated nuclear matrix protein that interacts with nucleophosmin/B23 protein.

Authors:  Younghwa Chun; Byoungwoo Park; Wansoo Koh; Sunhee Lee; Yeongmi Cheon; Raehyung Kim; Lihua Che; Soojin Lee
Journal:  J Biol Chem       Date:  2011-10-14       Impact factor: 5.157

2.  Reorganization of the nuclear compartments involved in transcription and RNA processing in myonuclei of type I spinal muscular atrophy.

Authors:  María S Castillo-Iglesias; María T Berciano; J Oriol Narcis; J Fernando Val-Bernal; José C Rodriguez-Rey; Olga Tapia; Miguel Lafarga
Journal:  Histochem Cell Biol       Date:  2019-06-11       Impact factor: 4.304

3.  RNA processing is altered in skeletal muscle nuclei of patients affected by myotonic dystrophy.

Authors:  Manuela Malatesta; Marzia Giagnacovo; Rosanna Cardani; Giovanni Meola; Carlo Pellicciari
Journal:  Histochem Cell Biol       Date:  2011-03-09       Impact factor: 4.304

4.  Bortezomib induces the formation of nuclear poly(A) RNA granules enriched in Sam68 and PABPN1 in sensory ganglia neurons.

Authors:  Iñigo Casafont; Maria T Berciano; Miguel Lafarga
Journal:  Neurotox Res       Date:  2009-07-16       Impact factor: 3.911

5.  Pre-mRNA processing is partially impaired in satellite cell nuclei from aged muscles.

Authors:  Manuela Malatesta; Federica Perdoni; Sylviane Muller; Carlo Pellicciari; Carlo Zancanaro
Journal:  J Biomed Biotechnol       Date:  2010-05-19

6.  Structural and functional alterations of the cell nucleus in skeletal muscle wasting: the evidence in situ.

Authors:  M Malatesta; G Meola
Journal:  Eur J Histochem       Date:  2010-10-19       Impact factor: 3.188

7.  Cultured myoblasts from patients affected by myotonic dystrophy type 2 exhibit senescence-related features: ultrastructural evidence.

Authors:  M Malatesta; M Giagnacovo; L V Renna; R Cardani; G Meola; C Pellicciari
Journal:  Eur J Histochem       Date:  2011-08-27       Impact factor: 3.188

Review 8.  RNA/MBNL1-containing foci in myoblast nuclei from patients affected by myotonic dystrophy type 2: an immunocytochemical study.

Authors:  F Perdoni; M Malatesta; R Cardani; M Giagnacovo; E Mancinelli; G Meola; C Pellicciari
Journal:  Eur J Histochem       Date:  2009-09-30       Impact factor: 3.188

Review 9.  Nuclei of aged myofibres undergo structural and functional changes suggesting impairment in RNA processing.

Authors:  M Malatesta; F Perdoni; S Muller; C Zancanaro; C Pellicciari
Journal:  Eur J Histochem       Date:  2009-06-29       Impact factor: 3.188

10.  The cell nuclei of skeletal muscle cells are transcriptionally active in hibernating edible dormice.

Authors:  Manuela Malatesta; Federica Perdoni; Serafina Battistelli; Sylviane Muller; Carlo Zancanaro
Journal:  BMC Cell Biol       Date:  2009-03-14       Impact factor: 4.241

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