Dataset Information

Mpe1 senses the polyadenylation signal in pre-mRNA to promote efficient cleavage and control polyadenylation

ABSTRACT: Crosslinking mass spectrometry dataset of the Mpe1 and Cft2 bound to the yeast CPF polymerase module. Sulfo-SDA is the crosslinker used.

ORGANISM(S): Saccharomyces Cerevisiae (baker's Yeast)

SUBMITTER: Juri Rappsilber

PROVIDER: PXD027482 | JPOST Repository | Thu Jan 12 00:00:00 GMT 2023

REPOSITORIES: jPOST

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Dataset's files

Source:

			Action	DRS
	B210320_15_Lumos_FO_CO_FO_Passmore_PAM1-CFT2-Mpe1-RNA_SDA_pepSEC5_rep1.raw	Raw
	B210320_16_Lumos_FO_CO_FO_Passmore_PAM1-CFT2-Mpe1-RNA_SDA_pepSEC5_rep2.raw	Raw
	B210320_17_Lumos_FO_CO_FO_Passmore_PAM1-CFT2-Mpe1-RNA_SDA_pepSEC6_rep1.raw	Raw
	B210320_18_Lumos_FO_CO_FO_Passmore_PAM1-CFT2-Mpe1-RNA_SDA_pepSEC6_rep2.raw	Raw
	B210320_19_Lumos_FO_CO_FO_Passmore_PAM1-CFT2-Mpe1-RNA_SDA_pepSEC7_rep1.raw	Raw

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Publications

Mpe1 senses the binding of pre-mRNA and controls 3' end processing by CPF.

Rodríguez-Molina Juan B JB O'Reilly Francis J FJ Fagarasan Holly H Sheekey Eleanor E Maslen Sarah S Skehel J Mark JM Rappsilber Juri J Passmore Lori A LA

Molecular cell 20220517 13

Most eukaryotic messenger RNAs (mRNAs) are processed at their 3' end by the cleavage and polyadenylation specificity factor (CPF/CPSF). CPF mediates the endonucleolytic cleavage of the pre-mRNA and addition of a polyadenosine (poly(A)) tail, which together define the 3' end of the mature transcript. The activation of CPF is highly regulated to maintain the fidelity of RNA processing. Here, using cryo-EM of yeast CPF, we show that the Mpe1 subunit directly contacts the polyadenylation signal sequ ...[more]

PMID: 35584695

Similar Datasets

Project description:Crosslink mass spectrometry datasets on sulfo-SDA-crosslinked affinity-purified RNA polymerase binders from SPA-pulldowns in E. coli K12, on rpoB-SPA / nusG-SPA / yacL-SPA. Cleared E. coli lysate was added to anti-FLAG M2 beads to isolate binders to rpoB (RNA polymerase), nusG or yacL (RNA polymerase binders). Elution was accomplished via TEV protease cleavage. pulldown eluate fractions were split. The heterobifunctional photoactivatable crosslinker sulfo-SDA (sulfosuccinimidyl 4,4′-azipentanoate) (Thermo Scientific Pierce, Waltham, MA, USA) was dissolved in modified lysis buffer (50 mM Hepes pH 7.2 at RT, 50 mM KCl, 10 mM NaCl, 1.5 mM MgCl2, 5% (v/v) glycerol) and immediately added to the samples at 50, 100, 250, 500 and 1000 µM. The crosslinking reaction proceeded in the dark for 2 h on ice. UV-crosslinking was achieved by irradiation with a UV laser at 365 nm for 15 seconds. Samples were frozen and stored at -20°C. Next, the samples were denatured by adding solid urea to give an 8 M solution, reduced using DTT at 10 mM following incubation at RT for 30 min and derivatized at 30 mM IAA over 20 min at RT and in the dark. LysC protease was added (protease:protein ratio ca. 1:100 (m/m)) and the samples digested for 4 h at 37°C. Then, the samples were diluted 1:5 with 100 mM ABC and trypsin was added at a ratio of approx. 1:50 (m/m). Digestion progressed for 16 h at 37 °C until stopping with TFA. Digests were cleaned up using C18 StageTips. Eluted peptides were fractionated using a Superdex Peptide 3.2/300 column (GE Healthcare) at a flow rate of 10 µl min−1 using 30% (v/v) acetonitrile and 0.1 % (v/v) trifluoroacetic acid as mobile phase(Leitner et al. 2012). Early 50 µl-fractions were collected, dried and stored at -20°C prior to LC-MS analysis. Each peptide fraction was acquired by LC-MS on a Fusion Lumos Tribrid mass spectrometer connected to an Ultimate 3000 RSLCnano system (Dionex, Thermo Fisher Scientific, Germany). Samples were resuspended in 1.6% acetonitrile 0.1% formic acid and injected onto an EASY-Spray column of 50 cm length (Thermo Scientific) running at 300 nl/min. Gradient elution using water with 0.1% formic acid and 80% acetonitrile with 0.1% formic acid was accomplished using optimised gradients for each SEC fraction (from 2% mobile phase B to 52.5% over 90 min, followed by a linear increase to 55% and 95% over 2.5 min each). Each fraction was analysed in duplicates. The settings of the mass spectrometer were as follows: Data-dependent mode with 2.5s-Top-speed setting; MS1 scan in Orbitrap at 120,000 resolution over 400 to 1,500 m/z; MS2-scan trigger only on precursors with z = 3-7+; fragmentation by HCD employing a decision tree logic with optimised collision energies; MS2 scan in Orbitrap at resolution of 60,000; dynamic exclusion was enabled upon single observation for 60 seconds. A recalibration of the precursor m/z was conducted based on high-confidence linear peptide identifications. The re-calibrated peak lists were searched against the sequences of proteins identified in a given pulldown along with their reversed sequences (as decoys) using xiSEARCH (v.1.7.6.2) for identification. MS-cleavability of the sulfo-SDA crosslinker was considered. Final crosslink lists were compiled using the identified candidates filtered to 2% FDR on residue pair-level and 5% on PPI-level with xiFDR v.2.1.5.