Literature DB >> 23275893

Nuclear routing networks span between nuclear pore complexes and genomic DNA to guide nucleoplasmic trafficking of biomolecules.

Marek Malecki1, Bianca Malecki.   

Abstract

In health and disease, biomolecules, which are involved in gene expression, recombination, or reprogramming have to traffic through the nucleoplasm, between nuclear pore complexes (NPCs) and genomic DNA (gDNA). This trafficking is guided by the recently revealed nuclear routing networks (NRNs).In this study, we aimed to investigate, if the NRNs have established associations with the genomic DNA in situ and if the NRNs have capabilities to bind the DNA de novo. Moreover, we aimed to study further, if nucleoplasmic trafficking of the histones, rRNA, and transgenes' vectors, between the NPCs and gDNA, is guided by the NRNs.We used Xenopus laevis oocytes as the model system. We engineered the transgenes' DNA vectors equipped with the SV40 LTA nuclear localization signals (NLS) and/or HIV Rev nuclear export signals (NES). We purified histones, 5S rRNA, and gDNA. We rendered all these molecules superparamagnetic and fluorescent for detection with nuclear magnetic resonance (NMR), total reflection x-ray fluorescence (TXRF), energy dispersive x-ray spectroscopy (EDXS), and electron energy loss spectroscopy (EELS).The NRNs span between the NPCs and genomic DNA. They form firm bonds with the gDNA in situ. After complete digestion of the nucleic acids with the RNases and DNases, the newly added DNA - modified with the dNTP analogs, bonds firmly to the NRNs. Moreover, the NRNs guide the trafficking of the DNA transgenes' vectors - modified with the SV40 LTA NLS, following their import into the nuclei through the NPCs. The pathway is identical to that of histones. The NRNs also guide the trafficking of the DNA transgenes' vectors, modified with the HIV Rev NES, to the NPCs, followed by their export out of the nuclei. Ribosomal RNAs follow the same pathway.To summarize, the NRNs are the structures connecting the NPCs and the gDNA. They guide the trafficking of the biomolecules between the NPCs and the gDNA.

Entities:  

Year:  2012        PMID: 23275893      PMCID: PMC3530191          DOI: 10.4172/2165-7491.1000112

Source DB:  PubMed          Journal:  J Fertili In Vitro        ISSN: 2165-7491


  75 in total

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Journal:  J Cell Sci       Date:  2012-02-01       Impact factor: 5.285

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Journal:  Wiley Interdiscip Rev RNA       Date:  2010-09-15       Impact factor: 9.957

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Journal:  J Biol Chem       Date:  2000-01-07       Impact factor: 5.157

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Journal:  Cell       Date:  2010-02-05       Impact factor: 41.582

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Journal:  Biophys J       Date:  2011-10-05       Impact factor: 4.033

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Journal:  Mol Biol Cell       Date:  1999-03       Impact factor: 4.138

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Journal:  J Cell Biol       Date:  1993-12       Impact factor: 10.539

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Journal:  J Cell Biol       Date:  1997-06-02       Impact factor: 10.539

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Authors:  C Strambio-de-Castillia; G Blobel; M P Rout
Journal:  J Cell Biol       Date:  1999-03-08       Impact factor: 10.539

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  2 in total

Review 1.  Nuclear trafficking of retroviral RNAs and Gag proteins during late steps of replication.

Authors:  Matthew S Stake; Darrin V Bann; Rebecca J Kaddis; Leslie J Parent
Journal:  Viruses       Date:  2013-11-18       Impact factor: 5.048

2.  Eradication of Human Ovarian Cancer Cells by Transgenic Expression of Recombinant DNASE1, DNASE1L3, DNASE2, and DFFB Controlled by EGFR Promoter: Novel Strategy for Targeted Therapy of Cancer.

Authors:  Marek Malecki; Jessica Dahlke; Melissa Haig; Lynn Wohlwend; Raf Malecki
Journal:  J Genet Syndr Gene Ther       Date:  2013-07-21
  2 in total

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