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Identification of PABPN1 interacting proteins by proximity labeling with TurboID coupled with mass spectrometry.
ORGANISM(S): Homo sapiens (Human) 
2023-08-04 | PXD039864 | Pride
Here, we present a 3'-Seq dataset of Pabpn1 KD LK cells and Scr control cells.
ORGANISM(S): Mus musculus 
We applied deep-sequencing based technique, 3'-Seq, to obtain comprehansive maps of poly-A sites in human cells. 3'-Seq was applied to two cell lines (U2OS and RPE-1), in control and PABPN1 knockdown cells Examination of poly-A sites in control and PABPN1kd cells (in two different cell lines)
ORGANISM(S): Homo sapiens 
Polyadenylation controls mRNA biogenesis, nuclear export, translation, and decay. These processes are interdependent and coordinately regulated by several poly(A)-binding proteins (PABPs). How PABPs are functionally regulated to control RNA fate is not fully understood. Here, we show that human PABP...
ORGANISM(S): Homo sapiens (Human) 
2024-10-17 | PXD047110 | Pride
Poly(A) binding protein nuclear 1 (PABPN1) is a multifunctional regulator of mRNA processing. PABPN1 inhibits alternative polyadenylation (APA), and in conditions with reduced PABPN1 levels APA utilization causes genome-wide mRNA dysregulation. PABPN1 levels decline from midlife onwards in Oculophar...
ORGANISM(S): Mus musculus (Mouse) 
2020-07-06 | PXD004865 | Pride
The DNA damage response (DDR) is an extensive signaling network that is robustly mobilized by DNA double-strand breaks (DSBs). The primary transducer of the DSB response is the protein kinase, ataxia-telangiectasia, mutated (ATM). Here, we establish nuclear poly(A)-binding protein 1 (PABPN1) as a no...
ORGANISM(S): Homo sapiens (Human) 
2017-11-30 | PXD005913 | Pride
PABPN1 effect on translation efficiency.
Nuclear mRNA metabolism is regulated by multiple proteins, which either directly bind to RNA or form multi-protein complexes. The RNA-binding protein ZC3H11A is involved in nuclear mRNA export, and NF-κB signaling and is essential during mouse embryo development. Furthermore, previous studies have s...
ORGANISM(S): Homo sapiens (Human) 
2023-10-24 | PXD042238 | Pride
Oculopharyngeal muscular dystrophy (OPMD) is an autosomal dominant disease caused by an alanine tract expansion mutation in Poly(A)-binding protein nuclear 1 (expPABPN1). To model OPMD in a myogenic and physiological context, we generated mouse myoblast cell clones stably expressing either human wil...
ORGANISM(S): Mus musculus 
3'-Seq LK Pabpn1 KD in vivo
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