scholarly journals A new yeast PUF family protein, Puf6p, represses ASH1 mRNA translation and is required for its localization

2004 ◽  
Vol 18 (12) ◽  
pp. 1452-1465 ◽  
Author(s):  
W. Gu
2019 ◽  
Vol 39 (6) ◽  
Author(s):  
Sumira Malik ◽  
Wijeong Jang ◽  
Song Yeon Park ◽  
Ji Young Kim ◽  
Ki-Sun Kwon ◽  
...  

Abstract Puf family proteins are translational regulators essential to a wide range of biological processes, including cell fate specification, stem cell self-renewal, and neural function. Yet, despite being associated with hundreds of RNAs, the underlying mechanisms of Puf target specification remain to be fully elucidated. In Drosophila, Pumilio – a sole Puf family protein – is known to collaborate with cofactors Nanos (Nos) and Brain Tumor (Brat); however, their roles in target specification are not clearly defined. Here, we identify Bag-of-marbles (Bam) as a new Pum cofactor in repression of Mothers against dpp (mad) mRNAs, for which Nos is known to be dispensable. Notably, our data show that Nos (but not Bam) was required for Pum association with hunchback (hb) mRNAs, a well-known target of Pum and Nos. In contrast, Bam (but not Nos) was required for Pum association with mad mRNAs. These findings show for the first time that Pum target specificity is determined not independently but in collaboration with cofactors.


Cell Research ◽  
2012 ◽  
Vol 23 (3) ◽  
pp. 320-322 ◽  
Author(s):  
Martin R Jakobsen ◽  
Trine H Mogensen ◽  
Søren R Paludan

2014 ◽  
Vol 65 (4) ◽  
pp. 1181-1191 ◽  
Author(s):  
Tengbo Huang ◽  
Randall A. Kerstetter ◽  
Vivian F. Irish

2007 ◽  
Vol 26 (6) ◽  
pp. 795-809 ◽  
Author(s):  
Nicolas Paquin ◽  
Marie Ménade ◽  
Guillaume Poirier ◽  
Damiane Donato ◽  
Emmanuel Drouet ◽  
...  

2019 ◽  
Author(s):  
James Papatzimas ◽  
Evgueni Gorobets ◽  
Ranjan Maity ◽  
Mir Ishruna Muniyat ◽  
Justin L. MacCallum ◽  
...  

<div> <div> <div> <p>Here we show the development of heterobifunctional small molecules capable of selectively targeting MCL1 using a Proteolysis Targeting Chimera (PROTAC) methodology leading to successful degradation. We have confirmed the involvement of the E3 ligase CUL4A-DDB1 cereblon (CRBN) ubiquitination pathway, making these PROTACs a first step toward a new class of anti-apoptotic BCL-2 family protein degraders. </p> </div> </div> </div>


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