Results 51 to 60 of about 17,120 (319)

Structure of spliceosomal ribonucleoproteins [PDF]

open access: yesF1000 Biology Reports, 2010
Splicing of the precursors of eukaryotic mRNA and some non-coding RNAs is catalyzed by the 'spliceosome', which comprises five RNA-protein complexes (small nuclear ribonucleoproteins, or snRNPs) that assemble in an ordered manner onto precursor-mRNAs. Much progress has been made in determining the gross morphology of spliceosomal assembly intermediates.
Kiyoshi Nagai   +2 more
openaire   +3 more sources

Pseudouridines in spliceosomal snRNAs [PDF]

open access: yesProtein & Cell, 2011
Spliceosomal RNAs are a family of small nuclear RNAs (snRNAs) that are essential for pre-mRNA splicing. All vertebrate spliceosomal snRNAs are extensively pseudouridylated after transcription. Pseudouridines in spliceosomal snRNAs are generally clustered in regions that are functionally important during splicing.
Andrew T. Yu, Junhui Ge, Yi-Tao Yu
openaire   +3 more sources

Srsf10 and the minor spliceosome control tissue-specific and dynamic SR protein expression

open access: yeseLife, 2020
Minor and major spliceosomes control splicing of distinct intron types and are thought to act largely independent of one another. SR proteins are essential splicing regulators mostly connected to the major spliceosome.
Stefan Meinke   +6 more
doaj   +1 more source

Dysregulation of global circular RNA abundance regulated by spliceosomes predicts prognosis in hepatocellular carcinoma

open access: yesHepatology Communications, 2022
CircRNAs have been reported to play crucial roles in tumor progression and recurrence, showing potential as biomarkers in cancer. However, the global abundance of circRNA and their involvement in hepatocellular carcinoma (HCC) development have not been ...
Lei He   +11 more
doaj   +1 more source

SF3b4: A Versatile Player in Eukaryotic Cells

open access: yesFrontiers in Cell and Developmental Biology, 2020
Spliceosomes are large protein-RNA complexes regulating pre-mRNA processing in eukaryotes. SF3b4 encodes a core subunit of the U2-type spliceosome, loss- or gain-of-function of which often associates with abnormal cell growth, leading to tumorigenesis ...
Feng Xiong, Sha Li, Sha Li
doaj   +1 more source

The MUC1 extracellular domain subunit is found in nuclear speckles and associates with spliceosomes. [PDF]

open access: yesPLoS ONE, 2012
MUC1 is a large transmembrane glycoprotein and oncogene expressed by epithelial cells and overexpressed and underglycosylated in cancer cells. The MUC1 cytoplasmic subunit (MUC1-C) can translocate to the nucleus and regulate gene expression.
Priyadarsini Kumar   +5 more
doaj   +1 more source

Dynamic Contacts of U2, RES, Cwc25, Prp8 and Prp45 Proteins with the Pre-mRNA Branch-Site and 3' Splice Site during Catalytic Activation and Step 1 Catalysis in Yeast Spliceosomes

open access: yesPLoS Genetics, 2015
Little is known about contacts in the spliceosome between proteins and intron nucleotides surrounding the pre-mRNA branch-site and their dynamics during splicing.
Cornelius Schneider   +5 more
semanticscholar   +1 more source

Brr2p-mediated conformational rearrangements in the spliceosome during activation and substrate repositioning [PDF]

open access: yes, 2012
Brr2p is one of eight RNA helicases involved in pre-mRNA splicing. Detailed understanding of the functions of Brr2p and other spliceosomal helicases has been limited by lack of knowledge of their in vivo substrates. To address this, sites of direct Brr2p–
Beggs, Jean D   +3 more
core   +1 more source

Splicing diversity revealed by reduced spliceosomes in C. merolae and other organisms

open access: yesRNA Biology, 2015
Pre-mRNA splicing has been considered one of the hallmarks of eukaryotes, yet its diversity is astonishing: the number of substrate introns for splicing ranges from hundreds of thousands in humans to a mere handful in certain parasites.
A. J. Hudson   +4 more
semanticscholar   +1 more source

Cellular bases of the RNA metabolism dysfunction in motor neurons of a murine model of spinal muscular atrophy: Role of Cajal bodies and the nucleolus [PDF]

open access: yes, 2017
Spinal muscular atrophy (SMA) is caused by a homozygous deletion or mutation in the survival motor neuron 1 (SMN1) gene that leads to reduced levels of SMN protein resulting in degeneration of motor neurons (MNs).
Berciano, Maria T.   +7 more
core   +2 more sources

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