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Second, the genome-wide mapping of putative TRX and PHB2 nuclear localizations reveals that both proteins display an exclusive nuclear localization. Such observations are consistent with the fact that PHB2 is able to interact with proteins of the splicing machinery ([@B3]), and TRX is able to interact with the ribonucleoprotein U1A, which is required for splicing ([@B28]).

Finally, we have shown that TRX and PHB2 display different subcellular localizations, a finding that agrees with the fact that PHB2 plays a role in the post-transcriptional maturation of mRNAs ([@B2], [@B3]). We therefore propose that TRX and PHB2 could share similar functions during cell proliferation, but that they are not redundant in this context.

Author Contributions

====================

AL conceived and designed the study, and wrote the manuscript. CB performed the experiments and helped to write the manuscript. JP helped to perform the experiments. AD participated to the data analysis. SR designed the study, coordinated the study and helped to write the manuscript.

Conflict of Interest Statement

==============================

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

**Funding.** This work was supported by the Agence Nationale pour la Recherche (ANR) and by a grant of the Fondation ARC pour la Recherche sur le Cerveau.

We acknowledge the technical help from the Microscopy and Cytometry platform of Institut Curie for the confocal microscopy.

Supplementary Material

======================

The Supplementary Material for this article can be found online at: 0b46394aab

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