TY - JOUR
T1 - Light modulation ameliorates expression of circadian genes and disease progression in spinal muscular atrophy mice
AU - Walter, Lisa M.
AU - Koch, Christiane E.
AU - Betts, Corinne A.
AU - Ahlskog, Nina
AU - Meijboom, Katharina E.
AU - van Westering, Tirsa L.E.
AU - Hazell, Gareth
AU - Bhomra, Amarjit
AU - Claus, Peter
AU - Oster, Henrik
AU - Wood, Matthew J.A.
AU - Bowerman, Melissa
PY - 2018/10/15
Y1 - 2018/10/15
N2 - Physiology and behaviour are critically dependent on circadian regulation via a core set of clock genes, dysregulation of which leads to metabolic and sleep disturbances. Metabolic and sleep perturbations occur in spinal muscular atrophy (SMA), a neuromuscular disorder caused by loss of the survival motor neuron (SMN) protein and characterized by motor neuron loss and muscle atrophy. We therefore investigated the expression of circadian rhythm genes in various metabolic tissues and spinal cord of the Taiwanese Smn-/-;SMN2 SMA animal model. We demonstrate a dysregulated expression of the core clock genes (clock, ARNTL/Bmal1, Cry1/2, Per1/2) and clock output genes (Nr1d1 and Dbp) in SMA tissues during disease progression. We also uncover an age- and tissue-dependent diurnal expression of the Smn gene. Importantly, we observe molecular and phenotypic corrections in SMA mice following direct light modulation. Our study identifies a key relationship between an SMA pathology and peripheral core clock gene dysregulation, highlights the influence of SMN on peripheral circadian regulation and metabolism and has significant implications for the development of peripheral therapeutic approaches and clinical care management of SMA patients.
AB - Physiology and behaviour are critically dependent on circadian regulation via a core set of clock genes, dysregulation of which leads to metabolic and sleep disturbances. Metabolic and sleep perturbations occur in spinal muscular atrophy (SMA), a neuromuscular disorder caused by loss of the survival motor neuron (SMN) protein and characterized by motor neuron loss and muscle atrophy. We therefore investigated the expression of circadian rhythm genes in various metabolic tissues and spinal cord of the Taiwanese Smn-/-;SMN2 SMA animal model. We demonstrate a dysregulated expression of the core clock genes (clock, ARNTL/Bmal1, Cry1/2, Per1/2) and clock output genes (Nr1d1 and Dbp) in SMA tissues during disease progression. We also uncover an age- and tissue-dependent diurnal expression of the Smn gene. Importantly, we observe molecular and phenotypic corrections in SMA mice following direct light modulation. Our study identifies a key relationship between an SMA pathology and peripheral core clock gene dysregulation, highlights the influence of SMN on peripheral circadian regulation and metabolism and has significant implications for the development of peripheral therapeutic approaches and clinical care management of SMA patients.
UR - http://www.scopus.com/inward/record.url?scp=85054382613&partnerID=8YFLogxK
U2 - 10.1093/hmg/ddy249
DO - 10.1093/hmg/ddy249
M3 - Journal articles
C2 - 29982483
AN - SCOPUS:85054382613
SN - 0964-6906
VL - 27
SP - 3582
EP - 3597
JO - Human Molecular Genetics
JF - Human Molecular Genetics
IS - 20
ER -