TY - JOUR
T1 - Modulation of DNA Repair Systems in Blind Cavefish during Evolution in Constant Darkness
AU - Zhao, Haiyu
AU - Di Mauro, Giuseppe
AU - Lungu-Mitea, Sebastian
AU - Negrini, Pietro
AU - Guarino, Andrea Maria
AU - Frigato, Elena
AU - Braunbeck, Thomas
AU - Ma, Hongju
AU - Lamparter, Tilman
AU - Vallone, Daniela
AU - Bertolucci, Cristiano
AU - Foulkes, Nicholas S.
PY - 2018
Y1 - 2018
N2 - How the environment shapes the function and evolution of DNA repair systems is poorly understood. In a comparative study using zebrafish and the Somalian blind cavefish, Phreatichthys andruzzii, we reveal that during evolution for millions of years in continuous darkness, photoreactivation DNA repair function has been lost in P. andruzzii. We demonstrate that this loss results in part from loss-of-function mutations in pivotal DNA-repair genes. Specifically, C-terminal truncations in P. andruzzii DASH and 6-4 photolyase render these proteins predominantly cytoplasmic, with consequent loss in their functionality. In addition, we reveal a general absence of light-, UV-, and ROS-induced expression of P. andruzzii DNA-repair genes. This results from a loss of function of the D-box enhancer element, which coordinates and enhances DNA repair in response to sunlight. Our results point to P. andruzzii being the only species described, apart from placental mammals, that lacks the highly evolutionary conserved photoreactivation function. We predict that in the DNA repair systems of P. andruzzii, we may be witnessing the first stages in a process that previously occurred in the ancestors of placental mammals during the Mesozoic era.
AB - How the environment shapes the function and evolution of DNA repair systems is poorly understood. In a comparative study using zebrafish and the Somalian blind cavefish, Phreatichthys andruzzii, we reveal that during evolution for millions of years in continuous darkness, photoreactivation DNA repair function has been lost in P. andruzzii. We demonstrate that this loss results in part from loss-of-function mutations in pivotal DNA-repair genes. Specifically, C-terminal truncations in P. andruzzii DASH and 6-4 photolyase render these proteins predominantly cytoplasmic, with consequent loss in their functionality. In addition, we reveal a general absence of light-, UV-, and ROS-induced expression of P. andruzzii DNA-repair genes. This results from a loss of function of the D-box enhancer element, which coordinates and enhances DNA repair in response to sunlight. Our results point to P. andruzzii being the only species described, apart from placental mammals, that lacks the highly evolutionary conserved photoreactivation function. We predict that in the DNA repair systems of P. andruzzii, we may be witnessing the first stages in a process that previously occurred in the ancestors of placental mammals during the Mesozoic era.
UR - https://res.slu.se/id/publ/97009
U2 - 10.1016/j.cub.2018.08.039
DO - 10.1016/j.cub.2018.08.039
M3 - Journal article
SN - 0960-9822
VL - 28
SP - 3229
EP - 3243
JO - Current Biology
JF - Current Biology
IS - 20
ER -