Although many RNA-protein complexes or ribonucleoproteins (RNPs) assemble spontaneously in vitro, little is known about how they form in the environment of a living cell. Insight into RNP assembly has come unexpectedly from functional analyses of the survival motor neuron (SMN) protein, a gene product that is affected in the neuromuscular disease spinal muscular atrophy. These studies show that the assembly of spliceosomal U-rich small nuclear RNPs in vivo depends on the activity of two large protein complexes, one of which contains the SMN protein. These complexes might also facilitate the assembly of other cellular RNPs
The assembly of the Sm‐class of uridine‐rich small nuclear ribonucleoproteins (U snRNPs), albeit spo...
Spinal Muscular Atrophy (SMA) is an often lethal autosomal recessive neurodegenerative disease that ...
Although spliceosomal Sm proteins can assemble spontaneously onto UsnRNA in vitro, this process requ...
Although many RNA-protein complexes or ribonucleoproteins (RNPs) assemble spontaneously in vitro, li...
Although many RNA-protein complexes or ribonucleoproteins (RNPs) assemble spontaneously in vitro, li...
Ribonucleoprotein complexes (RNPs) are involved in many essential cellular processes, of which the m...
Small nuclear ribonucleoproteins (snRNPs) are crucial for pre-mRNA processing to mRNAs. Each snRNP c...
Although spliceosomal Sm proteins can assemble spontaneously onto UsnRNA in vitro, this process requ...
In the cell, RNA exists and functions in a complex with RNA binding proteins (RBPs) that regulate ea...
International audienceSpinal muscular atrophy is a severe motor neuron disease caused by reduced lev...
This work is supported in part by the Royal Society via a University Research Fellowship.The biogene...
Pre-mRNA splicing is mediated by the spliceosome whose catalytic core is formed from uridine-rich sm...
AbstractMutation or deletion of one of the two genes encoding a protein known as SMN has recently be...
The splicing of pre-mRNA by the spliceosome is a characteristic feature of eukaryotic cells, depende...
Spinal muscular atrophy (SMA) is a motor neuron disease caused by reduced levels of the survival of ...
The assembly of the Sm‐class of uridine‐rich small nuclear ribonucleoproteins (U snRNPs), albeit spo...
Spinal Muscular Atrophy (SMA) is an often lethal autosomal recessive neurodegenerative disease that ...
Although spliceosomal Sm proteins can assemble spontaneously onto UsnRNA in vitro, this process requ...
Although many RNA-protein complexes or ribonucleoproteins (RNPs) assemble spontaneously in vitro, li...
Although many RNA-protein complexes or ribonucleoproteins (RNPs) assemble spontaneously in vitro, li...
Ribonucleoprotein complexes (RNPs) are involved in many essential cellular processes, of which the m...
Small nuclear ribonucleoproteins (snRNPs) are crucial for pre-mRNA processing to mRNAs. Each snRNP c...
Although spliceosomal Sm proteins can assemble spontaneously onto UsnRNA in vitro, this process requ...
In the cell, RNA exists and functions in a complex with RNA binding proteins (RBPs) that regulate ea...
International audienceSpinal muscular atrophy is a severe motor neuron disease caused by reduced lev...
This work is supported in part by the Royal Society via a University Research Fellowship.The biogene...
Pre-mRNA splicing is mediated by the spliceosome whose catalytic core is formed from uridine-rich sm...
AbstractMutation or deletion of one of the two genes encoding a protein known as SMN has recently be...
The splicing of pre-mRNA by the spliceosome is a characteristic feature of eukaryotic cells, depende...
Spinal muscular atrophy (SMA) is a motor neuron disease caused by reduced levels of the survival of ...
The assembly of the Sm‐class of uridine‐rich small nuclear ribonucleoproteins (U snRNPs), albeit spo...
Spinal Muscular Atrophy (SMA) is an often lethal autosomal recessive neurodegenerative disease that ...
Although spliceosomal Sm proteins can assemble spontaneously onto UsnRNA in vitro, this process requ...