scholarly journals An hypothesis concerning control networks and aging in Drosophila melanogaster and Caenorhabditis elegans

AGE ◽  
2001 ◽  
Vol 24 (4) ◽  
pp. 173-177
Author(s):  
Christopher Driver
2010 ◽  
Vol 188 (3) ◽  
pp. 313-323 ◽  
Author(s):  
Naomi R. Stevens ◽  
Jeroen Dobbelaere ◽  
Kathrin Brunk ◽  
Anna Franz ◽  
Jordan W. Raff

In Caenorhabditis elegans, five proteins are required for centriole duplication: SPD-2, ZYG-1, SAS-5, SAS-6, and SAS-4. Functional orthologues of all but SAS-5 have been found in other species. In Drosophila melanogaster and humans, Sak/Plk4, DSas-6/hSas-6, and DSas-4/CPAP—orthologues of ZYG-1, SAS-6, and SAS-4, respectively—are required for centriole duplication. Strikingly, all three fly proteins can induce the de novo formation of centriole-like structures when overexpressed in unfertilized eggs. Here, we find that of eight candidate duplication factors identified in cultured fly cells, only two, Ana2 and Asterless (Asl), share this ability. Asl is now known to be essential for centriole duplication in flies, but no equivalent protein has been found in worms. We show that Ana2 is the likely functional orthologue of SAS-5 and that it is also related to the vertebrate STIL/SIL protein family that has been linked to microcephaly in humans. We propose that members of the SAS-5/Ana2/STIL family of proteins are key conserved components of the centriole duplication machinery.


Gene ◽  
2001 ◽  
Vol 263 (1-2) ◽  
pp. 219-230 ◽  
Author(s):  
Ian G Frame ◽  
John F Cutfield ◽  
Russell T.M Poulter

Author(s):  
Raquel Borges de Barros Primo ◽  
Jacenir Vieira da Silva ◽  
Larissa P. Mueller ◽  
Flávio H. S. Araújo ◽  
Silvia Aparecida Oesterreich

2019 ◽  
Vol 14 (5) ◽  
pp. 1455-1488 ◽  
Author(s):  
Matthew A. Churgin ◽  
Milan Szuperak ◽  
Kristen C. Davis ◽  
David M. Raizen ◽  
Christopher Fang-Yen ◽  
...  

1992 ◽  
Vol 89 (9) ◽  
pp. 4168-4172 ◽  
Author(s):  
S. P. Rohrer ◽  
P. T. Meinke ◽  
E. C. Hayes ◽  
H. Mrozik ◽  
J. M. Schaeffer

Author(s):  
Justyna Mikuła-Pietrasik ◽  
Martyna Pakuła ◽  
Małgorzata Markowska ◽  
Paweł Uruski ◽  
Ludwina Szczepaniak-Chicheł ◽  
...  

Abstract Research on the evolutionary and mechanistic aspects of aging and longevity has a reductionist nature, as the majority of knowledge originates from experiments on a relatively small number of systems and species. Good examples are the studies on the cellular, molecular, and genetic attributes of aging (senescence) that are primarily based on a narrow group of somatic cells, especially fibroblasts. Research on aging and/or longevity at the organismal level is dominated, in turn, by experiments on Drosophila melanogaster, worms (Caenorhabditis elegans), yeast (Saccharomyces cerevisiae), and higher organisms such as mice and humans. Other systems of aging, though numerous, constitute the minority. In this review, we collected and discussed a plethora of up-to-date findings about studies of aging, longevity, and sometimes even immortality in several valuable but less frequently used systems, including bacteria (Caulobacter crescentus, Escherichia coli), invertebrates (Turritopsis dohrnii, Hydra sp., Arctica islandica), fishes (Nothobranchius sp., Greenland shark), reptiles (giant tortoise), mammals (blind mole rats, naked mole rats, bats, elephants, killer whale), and even 3D organoids, to prove that they offer biogerontologists as much as the more conventional tools. At the same time, the diversified knowledge gained owing to research on those species may help to reconsider aging from a broader perspective, which should translate into a better understanding of this tremendously complex and clearly system-specific phenomenon.


1998 ◽  
Vol 95 (15) ◽  
pp. 8744-8749 ◽  
Author(s):  
Y. Pekarsky ◽  
M. Campiglio ◽  
Z. Siprashvili ◽  
T. Druck ◽  
Y. Sedkov ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document