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Aldehyde-driven transcriptional stress triggers an anorexic DNA damage response

Mulderrig, Lee ; Garaycoechea, Juan I ; Tuong, Zewen K ; Millington, Christopher L ; Dingler, Felix A ; Ferdinand, John R ; Gaul, Liam ; Tadross, John A ; Arends, Mark J ; O'Rahilly, Stephen ; Crossan, Gerry P ; Clatworthy, Menna R ; Patel, Ketan J

Nature (London), 2021-12, Vol.600 (7887), p.158-163 [Periódico revisado por pares]

England: Nature Publishing Group

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Título:
Aldehyde-driven transcriptional stress triggers an anorexic DNA damage response
Autor: Mulderrig, Lee ; Garaycoechea, Juan I ; Tuong, Zewen K ; Millington, Christopher L ; Dingler, Felix A ; Ferdinand, John R ; Gaul, Liam ; Tadross, John A ; Arends, Mark J ; O'Rahilly, Stephen ; Crossan, Gerry P ; Clatworthy, Menna R ; Patel, Ketan J
Assuntos: Alcohol Dehydrogenase - deficiency ; Alcohol Dehydrogenase - metabolism ; Aldehydes ; Animals ; Anorexia ; Antibodies ; Aversion ; Body weight loss ; Brain - drug effects ; Brain - metabolism ; Brain - pathology ; Brain damage ; Brain injury ; Cachexia ; Cachexia - complications ; Chemotherapy ; Cockayne syndrome ; Cockayne Syndrome - chemically induced ; Cockayne Syndrome - complications ; Cockayne Syndrome - genetics ; Cockayne Syndrome - pathology ; Deoxyribonucleic acid ; Disease Models, Animal ; DNA ; DNA Damage ; DNA Repair Enzymes - deficiency ; DNA-directed RNA polymerase ; Female ; Food aversion ; Formaldehyde ; Formaldehyde - adverse effects ; Formaldehyde - metabolism ; Gene sequencing ; Genomes ; Genotype & phenotype ; Growth Differentiation Factor 15 - antagonists & inhibitors ; Growth Differentiation Factor 15 - biosynthesis ; Growth Differentiation Factor 15 - genetics ; Kidney Tubules, Proximal - drug effects ; Kidney Tubules, Proximal - metabolism ; Kidney Tubules, Proximal - pathology ; Kidneys ; Male ; Males ; Mice ; Mutation ; Neurodegeneration ; Poly-ADP-Ribose Binding Proteins - deficiency ; Renal failure ; Renal Insufficiency - complications ; Ribonucleic acid ; RNA ; RNA polymerase ; RNA polymerase II ; Stress, Physiological - drug effects ; Transcription ; Transcription, Genetic - drug effects ; Transcription, Genetic - genetics ; Weight loss
É parte de: Nature (London), 2021-12, Vol.600 (7887), p.158-163
Descrição: Endogenous DNA damage can perturb transcription, triggering a multifaceted cellular response that repairs the damage, degrades RNA polymerase II and shuts down global transcription . This response is absent in the human disease Cockayne syndrome, which is caused by loss of the Cockayne syndrome A (CSA) or CSB proteins . However, the source of endogenous DNA damage and how this leads to the prominent degenerative features of this disease remain unknown. Here we find that endogenous formaldehyde impedes transcription, with marked physiological consequences. Mice deficient in formaldehyde clearance (Adh5 ) and CSB (Csb ; Csb is also known as Ercc6) develop cachexia and neurodegeneration, and succumb to kidney failure, features that resemble human Cockayne syndrome. Using single-cell RNA sequencing, we find that formaldehyde-driven transcriptional stress stimulates the expression of the anorexiogenic peptide GDF15 by a subset of kidney proximal tubule cells. Blocking this response with an anti-GDF15 antibody alleviates cachexia in Adh5 Csb mice. Therefore, CSB provides protection to the kidney and brain against DNA damage caused by endogenous formaldehyde, while also suppressing an anorexic endocrine signal. The activation of this signal might contribute to the cachexia observed in Cockayne syndrome as well as chemotherapy-induced anorectic weight loss. A plausible evolutionary purpose for such a response is to ensure aversion to genotoxins in food.
Editor: England: Nature Publishing Group
Idioma: Inglês

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Aldehyde-driven transcriptional stress triggers an anorexic DNA damage response

Mulderrig, Lee ; Garaycoechea, Juan I ; Tuong, Zewen K ; Millington, Christopher L ; Dingler, Felix A ; Ferdinand, John R ; Gaul, Liam ; Tadross, John A ; Arends, Mark J ; O'Rahilly, Stephen ; Crossan, Gerry P ; Clatworthy, Menna R ; Patel, Ketan J

England: Nature Publishing Group

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