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   Protein Phosphatase 1 Down Regulates ZYG-1 Levels to Limit Centriole Duplication  
   
نویسنده peel n. ,iyer j. ,naik a. ,dougherty m.p. ,decker m. ,o’connell k.f.
منبع plos genetics - 2017 - دوره : 13 - شماره : 1
چکیده    In humans perturbations of centriole number are associated with tumorigenesis and microcephaly,therefore appropriate regulation of centriole duplication is critical. the c. elegans homolog of plk4,zyg-1,is required for centriole duplication,but our understanding of how zyg-1 levels are regulated remains incomplete. we have identified the two pp1 orthologs,gsp-1 and gsp-2,and their regulators i-2szy-2and sds-22 as key regulators of zyg-1 protein levels. we find that down-regulation of pp1 activity either directly,or by mutation of szy-2 or sds-22 can rescue the loss of centriole duplication associated with a zyg-1 hypomorphic allele. suppression is achieved through an increase in zyg-1 levels,and our data indicate that pp1 normally regulates zyg-1 through a post-translational mechanism. while moderate inhibition of pp1 activity can restore centriole duplication to a zyg-1 mutant,strong inhibition of pp1 in a wild-type background leads to centriole amplification via the production of more than one daughter centriole. our results thus define a new pathway that limits the number of daughter centrioles produced each cycle. © 2017 public library of science. all rights reserved.
آدرس department of biology,the college of new jersey,ewing,nj, United States, laboratory of biochemistry and genetics,national institute of diabetes,digestive and kidney diseases,national institutes of health,8 center drive,bethesda,md, United States, department of biology,the college of new jersey,ewing,nj, United States, laboratory of biochemistry and genetics,national institute of diabetes,digestive and kidney diseases,national institutes of health,8 center drive,bethesda,md, United States, max planck institute of molecular cell biology and genetics,dresden,0130,germany,genentech inc.,1 dna way,cancer immunology, United States, laboratory of biochemistry and genetics,national institute of diabetes,digestive and kidney diseases,national institutes of health,8 center drive,bethesda,md, United States
 
     
   
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