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			by Sarah Knapton 
			April 13, 
			2022 
			
			from
			
			Yahoo Website 
			
			
			
			Italian 
			version 
			
			 
			 
			 
			 
			
			  
			
			An elderly gentleman 
			
			  
			
			 
			 
			The mystery of why
			
			humans die at around 80, while 
			other mammals live far shorter or longer lives, may finally have 
			been solved by scientists. 
			 
			
			Humans and animals die after 
			amassing a similar number of genetic mutations, researchers have 
			found, suggesting the speed of DNA errors is critical in determining 
			the lifespan of a species. 
			 
			There are huge variations in the lifespan of mammals in the animal 
			kingdom, from South Asian rats, which live for just six months, to 
			bowhead whales, which can survive for 200 years. 
			 
			Previously, experts have suggested that size is the key to 
			longevity, with smaller animals burning up energy more quickly, 
			requiring a faster cell turnover, which causes a speedier decline. 
			 
			But a new study from the Wellcome Sanger Institute in 
			Cambridge suggests the speed of genetic damage could 
			be the key to survival, with long-living animals successfully 
			slowing down their rate of DNA mutations regardless of their size. 
			 
			It helps explain how a five-inch long naked mole rat can live for 25 
			years, about the same as a far larger giraffe, which typically lives 
			for 24. 
			
				
				When scientists 
				checked their mutation rates, they were surprisingly similar.
				 
			 
			
			Naked mole rats suffer 93 
			mutations a year and giraffes 99. 
  
			
			  
			
			
			
			  
			
			The study suggests it is the speed of genetic damage  
			
			that 
			could be the key to survival which helps explain  
			
			how a 
			giraffe typically lives for 24 years. 
			
			Thomas 
			Mukoya/Reuters 
			
			 
			 
			In contrast, mice suffer 796 mutations a year and only live for 3.7 
			years.  
			
			  
			
			The average human 
			lifespan in the study was 83.6 years, but the mutation rate was far 
			lower at around 47. 
			 
			Genetic changes, known as 
			
			somatic mutations, occur in all 
			cells and are largely harmless, but, 
			
				
				some can start a cell 
				on the path to cancer or impair normal functioning... 
			 
			
			Dr. Alex Cagan, 
			the first author of the study, said:  
			
				
				"To find a similar 
				pattern of genetic changes in animals as different from one 
				another as a mouse and a tiger was surprising." 
				 
				"But the most exciting aspect of the study has to be finding 
				that lifespan is inversely proportional to the somatic mutation 
				rate. This suggests that somatic mutations may play a role in 
				ageing." 
			 
			
			The team analyzed genetic 
			errors in the stem cells from the intestines of 16 species of mammal 
			and found that the longer the lifespan of a species, the slower the 
			rate at which mutations occur. 
			 
			The average number of mutations at the end of lifespan across 
			species was around 3200, suggesting there is a 
			critical mass of errors after which a body is unable to 
			function correctly. 
			
			  
			
			  
			
			  
			
			 
			'Ageing is a 
			complex process' 
			 
			Although the figure differed about threefold across species the 
			variation was far less than the variation in body size, which varied 
			up to 40,000 fold. 
			 
			The researchers believe the study (Somatic 
			Mutation Rates Scale with Lifespan across Mammals) opens 
			the door to understanding the ageing process, and the inevitability 
			and timing of death. 
			 
			Dr. Inigo Martincorena, the senior author of the study, said:
			 
			
				
				"Ageing is a complex 
				process, the result of multiple forms of molecular damage in our 
				cells and tissues. 
				 
				"Somatic mutations have been speculated to contribute to 
				ageing since the 1950s, but studying them has remained 
				difficult. 
				 
				"With the recent advances in 
				
				DNA sequencing technologies, 
				we can finally investigate the roles that somatic mutations play 
				in ageing and in multiple diseases." 
			 
			
			The research was 
			published in the 
			
			journal Nature... 
			 
  
			
			
			
			 
			
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