TY - JOUR
T1 - The latency of the light response is modulated by the phosphorylation state of Drosophila TRP at a specific site
AU - Katz, Ben
AU - Voolstra, Olaf
AU - Tzadok, Hanan
AU - Yasin, Bushra
AU - Rhodes-Modrov, Elisheva
AU - Bartels, Jonas Peter
AU - Strauch, Lisa
AU - Huber, Armin
AU - Minke, Baruch
PY - 2017/11/2
Y1 - 2017/11/2
N2 - Drosophila photoreceptors respond to oscillating light of high frequency (∼100 Hz), while increasing the oscillating light intensity raises the maximally detected frequency. Recently, we reported that dephosphorylation of the light-activated TRP ion channel at S936 is a fast, graded, light-, and Ca2+-dependent process. We further found that this process affects the detection limit of high frequency oscillating light. Accordingly, transgenic Drosophila, which do not undergo phosphorylation at the S936-TRP site (trpS936A), revealed a short time-interval before following the high stimulus frequency (oscillation-lock response) in both dark- and light-adapted flies. In contrast, the trpS936D transgenic flies, which mimic constant phosphorylation, showed a long-time interval to oscillation-lock response in both dark- and light-adapted flies. Here we extend these findings by showing that dark-adapted trpS936A flies reveal light-induced current (LIC) with short latency relative to trpWT or trpS936D flies, indicating that the channels are a limiting factor of response kinetics. The results indicate that properties of the light-activated channels together with the dynamic light-dependent process of TRP phosphorylation at the S936 site determine response kinetics.
AB - Drosophila photoreceptors respond to oscillating light of high frequency (∼100 Hz), while increasing the oscillating light intensity raises the maximally detected frequency. Recently, we reported that dephosphorylation of the light-activated TRP ion channel at S936 is a fast, graded, light-, and Ca2+-dependent process. We further found that this process affects the detection limit of high frequency oscillating light. Accordingly, transgenic Drosophila, which do not undergo phosphorylation at the S936-TRP site (trpS936A), revealed a short time-interval before following the high stimulus frequency (oscillation-lock response) in both dark- and light-adapted flies. In contrast, the trpS936D transgenic flies, which mimic constant phosphorylation, showed a long-time interval to oscillation-lock response in both dark- and light-adapted flies. Here we extend these findings by showing that dark-adapted trpS936A flies reveal light-induced current (LIC) with short latency relative to trpWT or trpS936D flies, indicating that the channels are a limiting factor of response kinetics. The results indicate that properties of the light-activated channels together with the dynamic light-dependent process of TRP phosphorylation at the S936 site determine response kinetics.
KW - TRP channel
KW - TRP dephosphorylation
KW - light induced current
KW - transgenic Drosophila
UR - http://www.scopus.com/inward/record.url?scp=85027846794&partnerID=8YFLogxK
U2 - 10.1080/19336950.2017.1361073
DO - 10.1080/19336950.2017.1361073
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C2 - 28762890
AN - SCOPUS:85027846794
SN - 1933-6950
VL - 11
SP - 678
EP - 685
JO - Channels
JF - Channels
IS - 6
ER -