Results 71 to 80 of about 2,120 (152)
Phase Separation: A New Dimension to Understanding Tumor Biology and Therapy
Liquid–liquid phase separation (LLPS) facilitates the assembly of biomolecular condensates by leveraging weak multivalent interactions. The low‐complexity domains, foldable domains of proteins, and nucleic acids provide multivalent interaction sites among different molecules and contribute to the formation of condensates.
Xingwen Wang +4 more
wiley +1 more source
Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy
FXR1P is a RNA binding protein involved in muscle development. Here, the authors show that mutations in FXR1 exon 15, which is alternatively spliced in muscle, cause multi-minicore myopathy in humans and in mouse models.
María Cristina Estañ +29 more
doaj +1 more source
Circadian Control of Protein Synthesis
The circadian clock maintains proteostasis in part through rhythmic control of protein synthesis. We propose that, across the day, translation alternates between distinct mechanisms to optimize energy efficiency and regulate complex assembly. This temporal compartmentalization produces alternating phases of slow specialized translation and rapid ...
Nathan R. James, John S. O'Neill
wiley +1 more source
Fbxo4-mediated degradation of Fxr1 suppresses tumorigenesis in head and neck squamous cell carcinoma
Fbxo4 tumour suppressor is part of a SCF E3 ligase which has two known substrates. Here, the authors identify Fxr1 as a substrate of SCFFbxo4 and identify an inherent regulatory feedback loop in head and neck squamous cell carcinoma that results in the ...
Shuo Qie +7 more
doaj +1 more source
Stress granules emerging during viral infection can play both pro‐ and antiviral roles. RNA viruses use various strategies to antagonize their formation, including the degradation, inhibition, or sequestration of G3BP1, a key stress granule protein. However, biochemical and structural insights into these mechanisms have been reported for only a handful
Moh Egy Rahman Firdaus +3 more
wiley +1 more source
Chromosome 3q26–28 is a critical region of genomic amplification in non-small cell lung cancer (NSCLC), particularly lung squamous cell carcinomas (SCCs).
Jun Qian +4 more
doaj +1 more source
Understanding GEMIN5 Interactions: From Structural and Functional Insights to Selective Translation
GEMIN5 structural domains. Overview of GEMIN5's role in snRNP assembly and translation regulatory events. ABSTRACT GEMIN5 is a predominantly cytoplasmic protein, initially identified as a member of the survival of motor neurons (SMN) complex. In addition, this abundant protein modulates diverse aspects of RNA‐dependent processes, executing its ...
Encarnacion Martinez‐Salas +2 more
wiley +1 more source
SKP1‐CUL1‐F‐box: Key molecular targets affecting disease progression
SCF complexes are widely involved in intracellular metabolism. In this paper, we discuss the diverse effects of SCF on crucial cellular processes such as cell cycle progression, cell migration, biological rhythms, DNA replication, cell differentiation, cell, apoptosis, immune response, and disease occurrence.
Xiangrong Zeng +6 more
wiley +1 more source
Genes and pathways differentially expressed in the brains of Fxr2 knockout mice
Fragile X syndrome is a common inherited form of mental retardation and originates from the absence of expression of the FMR1 gene. This gene and its two homologues, FXR1 and FXR2, encode for a family of fragile X related (FXR) proteins with similar ...
Sebastiano Cavallaro +5 more
doaj +1 more source
Comparative Genomic Sequence Analysis of the FXR Gene Family: FMR1, FXR1, and FXR2
Mutations in the X-linked gene FMR1 cause fragile X syndrome, the leading cause of inherited mental retardation. Two autosomal paralogs of FMR1 have been identified, and are known as FXR1 and FXR2. Here we describe and compare the genomic structures of the mouse and human genes FMR1, FXR1, and FXR2. All three genes are very well conserved from mouse to
L L, Kirkpatrick +2 more
openaire +2 more sources

