Papers on
PRP9
Spp382p interacts with multiple yeast splicing factors, including possible regulators of Prp43 DExD/H-Box protein function.Rymond et al., Lexington, United States. In Genetics, 2009
Identified, among others, are genes encoding the established splicing factors Prp8p, Prp9p, Prp11p, Prp39p, and Yhc1p and two poorly characterized proteins with possible links to splicing, Sqs1p and Cwc23p.
Discovery of eight novel divergent homologs expressed in cattle placenta.Lewin et al., Urbana, United States. In Physiol Genomics, 2006
These were named as follows: cattle cerebrum and skeletal muscle-specific transcript 1 (CSSMST1), cattle intestine-specific transcript 1 (CIST1), hepatitis A virus cellular receptor 1 amino-terminal domain-containing protein (HAVCRNDP), prolactin-related proteins 8, 9, and 11 (PRP8, PRP9, and PRP11, respectively) and secreted and transmembrane protein 1A and 1B (SECTM1A and SECTM1B, respectively).
Structure-function analysis of the U2 snRNP-associated splicing factor SF3a.Tanackovic et al., Genève, Switzerland. In Biochem Soc Trans, 2005
Studies aimed at the identification of regions in SF3a60 and SF3a66, required for proper intracellular localization, have led to a model for the final steps in U2 snRNP biogenesis and the proposal that SF3a is incorporated into the U2 snRNP in Cajal bodies.
Proteomic analysis identifies a new complex required for nuclear pre-mRNA retention and splicing.Séraphin et al., Gif-sur-Yvette, France. In Embo J, 2005
While SF3a purification revealed only the expected subunits Prp9p, Prp11p and Prp21p, yeast SF3b was found to contain only six subunits, including previously known components (Rse1p, Hsh155p, Cus1p, Hsh49p), the recently identified Rds3p factor and a new small essential protein (Ysf3p) encoded by an unpredicted split ORF in the yeast genome.
Molecular hierarchy in neurons differentiated from mouse ES cells containing a single human chromosome 21.Oshimura et al., Hong Kong, Hong Kong. In Biochem Biophys Res Commun, 2004
Defective neuronal differentiation in the presence of extra hChr21 manifested primarily the post-transcriptional and translational modification, such as Mrpl10, SNAPC3, Srprb, SF3a60 in the early neuronal stem cell stage, and Mrps18a, Eef1g, and Ubce8 in the late differentiated stage.