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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
Mol Cancer Res. Author manuscript; available in PMC 2011 January 12.
Published in final edited form as:
PMCID: PMC2808419

P58TFL does not localize to messenger RNA processing bodies

The messenger RNA processing body (P-body) is a cellular structure that has a critical role in the regulation of mRNA translation, storage, transport and degradation (reviewed in 13). In a recent study published in Molecular Cancer Research, Minagawa et al. (4) reported that p58TFL fused to green fluorescent protein (GFP), when co-expressed with P-body components HA-DCP1a or HA-EIF2C2, localized to P-bodies. p58TFL is a member of the ZCH12 zinc finger family of proteins and may regulate cell growth by suppressing retinoblastoma protein phosphorylation. Because the regulation of the cell cycle and cell growth would be new functions for P-bodies, we attempted to confirm the observation that p58TFL is a P-body component.

The plasmid encoding p58TFL-GFP was obtained from Minagawa and colleagues and transfected into human epidermoid carcinoma cell line Hep-2. Cells were stained with anti-GFP antiserum and with antibodies directed against endogenous P-body markers Ge-1/HEDLS (5), RAP55 (6) or DCP1a (7). p58TFL-GFP localized to dot-like structures throughout the cell (Figure 1a, d, and g), as reported (4). However, p58TFL-GFP did not co-localize with Ge-1 (a–c), RAP55 (d–f), or DCP1a (g–i). The same results were observed whether cells were permeabilized with methanol (Figure 1) or Triton X-100 (not shown). In addition, p58TFL-GFP did not co-localize with P-body markers when expressed in a second cell line (murine fibroblast cell line 3T3, not shown). These results confirm that p58TFL-GFP forms dot-like structures in mammalian cells as previously reported. However, p58TFL-GFP-containing structures are distinct from P-bodies.

Figure 1
p58TFL-GFP does not localize to P-bodies. When expressed in Hep-2 cells, p58TFL-GFP localized to dot-like structures throughout the cell (green, a, d, and g). However, p58TFL-GFP did not co-localize with antibodies directed against P-body markers Ge-1, ...


1. Franks TM, Lykke-Andersen J. The control of mRNA decapping and P-body formation. Mol Cell. 2008;32(5):605–615. [PMC free article] [PubMed]
2. Parker R, Sheth U. P bodies and the control of mRNA translation and degradation. Mol Cell. 2007;25(5):635–646. [PubMed]
3. Eulalio A, Behm-Ansmant I, Izaurralde E. P bodies: at the crossroads of posttranscriptional pathways. Nat Rev Mol Cell Biol. 2007;8(1):9–22. [PubMed]
4. Minagawa K, Katayama Y, Nishikawa S, Yamamoto K, Sada A, Okamura A, et al. Inhibition of G(1) to S phase progression by a novel zinc finger protein P58(TFL) at P-bodies. Mol Cancer Res. 2009;7(6):880–889. [PubMed]
5. Yu JH, Yang WH, Gulick T, Bloch KD, Bloch DB. Ge-1 is a central component of the mammalian cytoplasmic mRNA processing body. RNA. 2005;11:1795–1802. [PubMed]
6. Yang WH, Yu JH, Gulick T, Bloch KD, Bloch DB. RNA-associated protein 55 (RAP55) localizes to mRNA processing bodies and stress granules. RNA. 2006;12(4):547–554. [PubMed]
7. Lykke-Andersen J. Identification of a human decapping complex associated with hUpf proteins in nonsense-mediated decay. Mol Cell Biol. 2002;22(23):8114–8121. [PMC free article] [PubMed]