scholarly journals Gene Expression in Parp1 Deficient Mice Exposed to a Median Lethal Dose of Gamma Rays

2018 ◽  
Vol 190 (1) ◽  
pp. 53 ◽  
Author(s):  
M. A. Suresh Kumar ◽  
Evagelia C. Laiakis ◽  
Shanaz A. Ghandhi ◽  
Shad R. Morton ◽  
Albert J. Fornace, Jr. ◽  
...  
2017 ◽  
Vol 4 (04) ◽  
Author(s):  
ANURADHA PATEL ◽  
POONAM VERMA ◽  
SHARDA CHOUDHARY ◽  
ARVIND KUMAR VERMA

Fenugreek (Trigonella foenum-graecumL.) is an annual crop, mainly used as a spiceand leafy vegetable crop in many parts of the world. Classical breeding in fenugreek is restricted due to its low genetic variability and small flower size which hamper manual emasculation and pollination. Mutation breeding is an effective way to enrich genetic variability in crop plants. An experiment was conducted to determine the lethal dose of the physical mutagen gamma rays in fenugreek. The dry seeds of fenugreek were exposed to different doses of gamma rays i.e. 150Gy, 200Gy, 250Gy, 300Gy and 350Gy. These irradiated seeds were sown in the Petri plates with non-irradiated seeds (control). As the dose of gamma rays increased, there was a decrease in germination percentage, seedling survival, root length, shoot length and vigour index. Among five doses of gamma rays, the maximum seed germination was observed at lowest dose 150Gy (93%), followed by 200Gy (83%), 250Gy (76%), 300Gy (76%) and 350Gy (64%). The seedling survival was decreased from 90% (in control) to 56% in 350Gy dose of gamma rays. The gamma rays dose of 150Gy gave stimulatory effect on seedlings growth. The growth parameters were dose dependent, as the dose of gamma rays increased from 200Gy to 350Gy. The gamma rays dose of 350Gy showed 64% seeds germination and 56% of seedlings survival. Therefore, it is concluded that the LD50 dose for fenugreek is close to 350Gy. This information would be highly useful for initiating mutation breeding programme in fenugreek


2001 ◽  
Vol 159 (5) ◽  
pp. 1949-1956 ◽  
Author(s):  
Jack Lawler ◽  
Wei-Min Miao ◽  
Mark Duquette ◽  
Noël Bouck ◽  
Roderick T. Bronson ◽  
...  

2002 ◽  
Vol 12 (2) ◽  
pp. 137-147 ◽  
Author(s):  
G. E. Kelly ◽  
J. K. Lindsey

2006 ◽  
Vol 99 (2) ◽  
pp. 499-513 ◽  
Author(s):  
Beatrice A. Girard ◽  
Vincent Lelievre ◽  
Karen M. Braas ◽  
Tannaz Razinia ◽  
Margaret A. Vizzard ◽  
...  

2017 ◽  
Vol 37 (11) ◽  
pp. 2053-2063 ◽  
Author(s):  
Charlotte Trenteseaux ◽  
Anh-thu Gaston ◽  
Audrey Aguesse ◽  
Guillaume Poupeau ◽  
Pierre de Coppet ◽  
...  

Objective— Experimental studies suggest that maternal hypercholesterolemia may be relevant for the early onset of cardiovascular disease in offspring. We investigated the effect of perinatal hypercholesterolemia on the atherosclerosis development in the offspring of apolipoprotein E–deficient mice and the underlying mechanism. Approach and Results— Atherosclerosis and related parameters were studied in adult male or female apolipoprotein E–deficient mice offspring from either normocholesterolemic or hypercholesterolemic mothers and normocholesterolemic fathers. Female born to hypercholesterolemic mothers had more aortic root lesions than female born to normocholesterolemic mothers. Lesions in whole aorta did not differ between groups. Higher trimethylamine-N-oxide levels and Fmo3 hepatic gene expression were higher in female born to hypercholesterolemic mothers offspring compared with female born to normocholesterolemic mothers and male. Trimethylamine-N-oxide levels were correlated with the size of atherosclerotic root lesions. Levels of hepatic cholesterol and gallbladder bile acid were greater in male born to hypercholesterolemic mothers compared with male born to normocholesterolemic mothers. At 18 weeks of age, female born to hypercholesterolemic mothers showed lower hepatic Scarb1 and Cyp7a1 but higher Nr1h4 gene expression compared with female born to normocholesterolemic mothers. Male born to hypercholesterolemic mothers showed an increase in Scarb1 and Ldlr gene expression compared with male born to normocholesterolemic mothers. At 25 weeks of age, female born to hypercholesterolemic mothers had lower Cyp7a1 gene expression compared with female born to normocholesterolemic mothers. DNA methylation of Fmo3, Scarb1 , and Ldlr promoter regions was slightly modified and may explain the mRNA expression modulation. Conclusions— Our findings suggest that maternal hypercholesterolemia may exacerbate the development of atherosclerosis in female offspring by affecting metabolism of trimethylamine-N-oxide and bile acids. These data could be explained by epigenetic alterations.


2011 ◽  
Vol 34 (3) ◽  
pp. 386-395 ◽  
Author(s):  
Yan Jiao ◽  
Jifei Zhang ◽  
Jian Yan ◽  
John Stuart ◽  
Griffin Gibson ◽  
...  

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