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https://read.qxmd.com/read/38345056/association-of-systemic-markers-of-inflammation-with-signs-and-symptoms-of-dry-eye-disease-and-sjogren-s-syndrome-in-the-dry-eye-assessment-and-management-dream%C3%A2-study
#1
JOURNAL ARTICLE
Marium H Hashemi, Julian L Ambrus, Abhay A Shukla, Di Zhu, Gui-Shuang Ying, Penny A Asbell
PURPOSE: To evaluate the possible role of systemic inflammation in dry eye disease (DED) via systemic inflammatory marker associations with DED signs and symptoms, and an analysis of a subgroup with Sjogren's Syndrome (SS). METHODS: Participant serums were analyzed using line immunoassays (LIAs) for the presence of antibodies against 34 systemic inflammatory markers. Using the 2012 American College of Rheumatology definition, the 481 participants were categorized into group 1 (SS; n  = 52), group 2 (autoimmune disease not including SS; n  = 66), or group 3 (control, i...
February 12, 2024: Current Eye Research
https://read.qxmd.com/read/32352217/hepatitis-delta-virus-interacts-with-splicing-factor-sf3b155-and-alters-pre-mrna-splicing-of-cell-cycle-control-genes
#2
JOURNAL ARTICLE
João Paulo Tavanez, Rafael Caetano, Cristina Branco, Inês Margarida Brito, Ana Miragaia-Pereira, Tatiana Vassilevskaia, Ana Sofia Quina, Celso Cunha
Hepatitis delta virus (HDV) is the agent responsible for the most severe form of human viral hepatitis. The HDV genome consists of a single-stranded circular RNA molecule that encodes for one single protein, the delta antigen. Given its simplicity, HDV must make use of several host cellular proteins to accomplish its life cycle processes, including transcription, replication, post-transcriptional, and post-translational modifications. Consequently, identification of the interactions established between HDV components and host proteins assumes a pivotal interest in the search of novel therapeutic targets...
September 2020: FEBS Journal
https://read.qxmd.com/read/28935704/the-splicing-co-factor-barricade-tat-sf1-is-required-for-cell-cycle-and-lineage-progression-in-drosophila-neural-stem-cells
#3
JOURNAL ARTICLE
Monika K Abramczuk, Thomas R Burkard, Vivien Rolland, Victoria Steinmann, Peter Duchek, Yanrui Jiang, Sebastian Wissel, Heinrich Reichert, Juergen A Knoblich
Stem cells need to balance self-renewal and differentiation for correct tissue development and homeostasis. Defects in this balance can lead to developmental defects or tumor formation. In recent years, mRNA splicing has emerged as an important mechanism regulating cell fate decisions. Here we address the role of the evolutionarily conserved splicing co-factor Barricade (Barc)/Tat-SF1/CUS2 in Drosophila neural stem cell (neuroblast) lineage formation. We show that Barc is required for the generation of neurons during Drosophila brain development by ensuring correct neural progenitor proliferation and differentiation...
November 1, 2017: Development
https://read.qxmd.com/read/28432478/the-arabidopsis-splicing-factors-atu2af65-atu2af35-and-atsf1-shuttle-between-nuclei-and-cytoplasms
#4
JOURNAL ARTICLE
Hyo-Young Park, Keh Chien Lee, Yun Hee Jang, Soon-Kap Kim, May Phyo Thu, Jeong Hwan Lee, Jeong-Kook Kim
The Arabidopsis splicing factors, AtU2AF65, AtU2AF35, and AtSF1 shuttle between nuclei and cytoplasms. These proteins also move rapidly and continuously in the nuclei, and their movements are affected by ATP depletion. The U2AF65 proteins are splicing factors that interact with SF1 and U2AF35 proteins to promote U2snRNP for the recognition of the pre-mRNA 3' splice site during early spliceosome assembly. We have determined the subcellular localization and movement of these proteins' Arabidopsis homologs. It was found that Arabidopsis U2AF65 homologs, AtU2AF65a, and AtU2AF65b proteins interact with AtU2AF35a and AtU2AF35b, which are Arabidopsis U2AF35 homologs...
July 2017: Plant Cell Reports
https://read.qxmd.com/read/28119336/large-scale-analysis-of-branchpoint-usage-across-species-and-cell-lines
#5
JOURNAL ARTICLE
Allison J Taggart, Chien-Ling Lin, Barsha Shrestha, Claire Heintzelman, Seongwon Kim, William G Fairbrother
The coding sequence of each human pre-mRNA is interrupted, on average, by 11 introns that must be spliced out for proper gene expression. Each intron contains three obligate signals: a 5' splice site, a branch site, and a 3' splice site. Splice site usage has been mapped exhaustively across different species, cell types, and cellular states. In contrast, only a small fraction of branch sites have been identified even once. The few reported annotations of branch site are imprecise as reverse transcriptase skips several nucleotides while traversing a 2-5 linkage...
April 2017: Genome Research
https://read.qxmd.com/read/20094034/the-intronic-splicing-code-multiple-factors-involved-in-atm-pseudoexon-definition
#6
JOURNAL ARTICLE
Ashish Dhir, Emanuele Buratti, Maria A van Santen, Reinhard Lührmann, Francisco E Baralle
Abundance of pseudo splice sites in introns can potentially give rise to innumerable pseudoexons, outnumbering the real ones. Nonetheless, these are efficiently ignored by the splicing machinery, a process yet to be understood completely. Although numerous 5' splice site-like sequences functioning as splicing silencers have been found to be enriched in predicted human pseudoexons, the lack of active pseudoexons pose a fundamental challenge to how these U1snRNP-binding sites function in splicing inhibition. Here, we address this issue by focusing on a previously described pathological ATM pseudoexon whose inhibition is mediated by U1snRNP binding at intronic splicing processing element (ISPE), composed of a consensus donor splice site...
February 17, 2010: EMBO Journal
https://read.qxmd.com/read/12036604/cloning-the-cdna-for-murine-u2-snrnp-a-gene-and-its-differential-expression-in-lymphocyte-development
#7
JOURNAL ARTICLE
Mariastefania Antica, Borka Kusic, Dubravka Hranilovic, Allan B Dietz, Stanimir Vuk-Pavlovic
We studied genes differentially transcribed during development of murine thymocytes. By the use of differential display of mRNA by polymerase chain reaction (DD-PCR) we identified a cDNA for U2snRNP-A' from a transcript abundant in precursor thymocytes, but rare in mature T cells. The transcript was fully cloned and found to be 97% homologous to the human cDNA for U2 snRNP-A'. We found the gene most abundantly transcribed on day 15 of gestation and in adult prothymocytes, spleen, testis and liver. Further characterization of snRNP proteins in the mouse is warranted in an effort to establish animal models of autoimmunity relevant for studies of connective tissue diseases or systemic lupus erythematosus, where patients harbor autoantibodies reactive to snRNP...
July 3, 2002: Immunology Letters
https://read.qxmd.com/read/11156603/multiple-roles-for-the-yeast-sub2-yuap56-gene-in-splicing
#8
JOURNAL ARTICLE
D Libri, N Graziani, C Saguez, J Boulay
The UAP56 gene has been shown to be required for prespliceosome assembly in mammals. We report here the isolation of the Schizosaccharomyces pombe ortholog of this gene by heterologous complementation of a combined PRP40HA(3)/nam8Delta defect in budding yeast. The Saccharomyces cerevisiae ortholog, YDL084w/SUB2, is also able to suppress this defect. We show that SUB2 is involved in splicing in vivo as well as in vitro. Sub2 defective extracts form a stalled intermediate that contains U2snRNP and can be chased into functional spliceosomes...
January 1, 2001: Genes & Development
https://read.qxmd.com/read/9404895/identification-of-a-novel-non-snrnp-protein-complex-containing-u1a-protein
#9
JOURNAL ARTICLE
J P O'Connor, J C Alwine, C S Lutz
Mouse monoclonal antibodies (MAbs) were generated against Escherichia coli-produced U1snRNP-A (U1A) protein. U1A-specific MAbs as well as MAbs that reacted with both U1A and U2snRNP-B" (U2B") were isolated. MAb 12E12 was unique among the characterized MAbs because it failed to immunoprecipitate U1A protein produced by in vitro transcription and translation using rabbit reticulocyte lysates. However, when U1A protein was made using a wheat germ extract, MAb 12E12 could immunoprecipitate U1A quite readily, as did the other MAbs...
December 1997: RNA
https://read.qxmd.com/read/1833724/evolutionary-conservation-of-the-spliceosomal-protein-u2b
#10
JOURNAL ARTICLE
G G Simpson, P Vaux, G Clark, R Waugh, J D Beggs, J W Brown
U1 and U2snRNPs play key roles in pre-mRNA splicing. The interactions between the U1 and U2snRNP-specific proteins, U1A, U2A' and U2B'' and their respective UsnRNAs are of interest both to elucidate their roles in splicing, and as models to study RNA-protein interactions. We have cloned a full-length cDNA, encoding U2B'', from potato. This is the first report of a sequence for a plant UsnRNP protein. The plant U2B'' sequence exhibits extensive similarity with the human U2B'' protein at both the DNA and amino acid levels...
October 11, 1991: Nucleic Acids Research
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