Faculty Opinions recommendation of DNA-PKcs-dependent signaling of DNA damage in Dictyostelium discoideum.

Author(s):  
John Rouse
1989 ◽  
Vol 50 (1) ◽  
pp. 69-73 ◽  
Author(s):  
Kumio Okaichi ◽  
Nobuyuki Kajitani ◽  
Katuko Nakajima ◽  
Keiichi Nozu ◽  
Takeo Ohnishi

Cell Cycle ◽  
2006 ◽  
Vol 5 (7) ◽  
pp. 702-708 ◽  
Author(s):  
Duen-Wei Hsu ◽  
Pascale Gaudet ◽  
Jessica J. R. Hudson ◽  
Catherine J. Pears ◽  
Nicholas D. Lakin

Genetics ◽  
1982 ◽  
Vol 102 (4) ◽  
pp. 711-723
Author(s):  
Dennis L Welker ◽  
Birgit A Metz ◽  
Keith L Williams

ABSTRACT A tandem duplication (D350(III,III)) of the whiB to radB interval of linkage group III has been characterized. The gene order on the duplication-bearing chromosome is: centromere, whiB500, radB+, whiB+, radB24, bsgA5, acrC4. Slow-growing, duplication-bearing strains (yellow-spored, radiation-resistant) produced four classes of faster growing sectors involving the whiB and radB loci: white-spored, radiation-sensitive (whiB500, radB24); white-spored, radiation-resistant (whiB500, radB+); yellow-spored, radiation-sensitive (whiB+, radB24); and yellow-spored, radiation-resistant. The first three classes can be explained as the products of single recombination events in which one copy of the whiB to radB interval was lost. The yellow-spored, radiation-resistant sectors probably arose by mutation elsewhere in the genome, but alternatively may represent multiple recombination events or deletion of part of one copy of the duplicated region. Loss of the duplicated segment was enhanced by irradiation with ultraviolet light (254 nm). Heterozygosity for a DNA repair mutation at the radB locus may have been involved in the formation of the duplication. It is proposed that translocations are a major cause of nonrandom segregation patterns such as the cosegregation of unlinked markers in Dictyostelium discoideum. Translocations involving all known linkage groups are tabulated and DNA damage by N-methyl-N′-nitro-N-nitrosoguanidine is implicated in the formation of translocations in D. discoideum.


2005 ◽  
Vol 15 (20) ◽  
pp. 1880-1885 ◽  
Author(s):  
Jessica J.R. Hudson ◽  
Duen-Wei Hsu ◽  
Kunde Guo ◽  
Natasha Zhukovskaya ◽  
Po-Hsien Liu ◽  
...  

Cells ◽  
2019 ◽  
Vol 8 (11) ◽  
pp. 1406 ◽  
Author(s):  
Javier Rodriguez-Centeno ◽  
Rosario Perona ◽  
Leandro Sastre

Dyskerin is a protein involved in the formation of small nucleolar and small Cajal body ribonucleoproteins. These complexes participate in RNA pseudouridylation and are also components of the telomerase complex required for telomere elongation. Dyskerin mutations cause a rare disease, X-linked dyskeratosis congenita, with no curative treatment. The social amoeba Dictyostelium discoideum contains a gene coding for a dyskerin homologous protein. In this article D. discoideum mutant strains that have mutations corresponding to mutations found in dyskeratosis congenita patients are described. The phenotype of the mutant strains has been studied and no alterations were observed in pseudouridylation activity and telomere structure. Mutant strains showed increased proliferation on liquid culture but reduced growth feeding on bacteria. The results obtained indicated the existence of increased DNA damage response and reactive oxygen species, as also reported in human Dyskeratosis congenita cells and some other disease models. These data, together with the haploid character of D. discoideum vegetative cells, that resemble the genomic structure of the human dyskerin gene, located in the X chromosome, support the conclusion that D. discoideum can be a good model system for the study of this disease.


2004 ◽  
Vol 171 (4S) ◽  
pp. 416-416
Author(s):  
Tamer M. Said ◽  
Shyam Allamaneni ◽  
Kiran P. Nallella ◽  
Rakesh K. Sharma ◽  
Sijo J. Parekattil ◽  
...  

Nature ◽  
2020 ◽  
Vol 579 (7800) ◽  
pp. 499-500
Author(s):  
Irene Gallina ◽  
Julien P. Duxin
Keyword(s):  

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