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. 2019 Apr 10;10:735. doi: 10.3389/fmicb.2019.00735

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Copyright © 2019 Panzer, Brych, Batschauer and Terpitz.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Light regulation of (A) Umops1 and (B) Umops2 expression. Transcript levels were quantified by qRT-PCR. FB1 cells were grown in complete darkness and then illuminated with monochromatic lights at a fluence rate of 10 μmol/m²/s¹ for 1 h. Transcript levels were normalized against the one of Umops1 in dark-grown wild type and cyclophilin. Shown are means and SD of three biological replicates kept in darkness or illuminated with either blue (λ_max 471 nm), red (λ_max 664 nm), or far-red (λ_max 740 nm) light as indicated. Significance levels between group samples are indicated for p-values over 0.05 with not significant (n.s.), for <0.05 with one asterisk (^∗), for <0.01 with two asterisks (^∗∗), and for <0.001 with three asterisks (^∗∗∗). Note that relative transcript levels are given in logarithmic scale.