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Series GSE201901 Query DataSets for GSE201901
Status Public on Dec 16, 2022
Title A role for gene expression and mRNA stability in nutritional compensation of the circadian clock
Organism Neurospora crassa
Experiment type Expression profiling by high throughput sequencing
Summary To identify the role of the cleavage and polyadenylation CFIm complex (NCU02152 and NCU09014) in the circadian clock, mRNA 3' End Sequencing was performed on a knockout mutant and compared to control samples.
Hundreds of polyadenylation sites are affected by loss of CFIm complex activity in Neurospora crassa.
 
Overall design 3' End Sequencing was performed on biological duplicate samples from 25C, constant light cultures grown for 72 hours to identify poly(A) tail locations.
 
Contributor(s) Kelliher CM, Stevenson E, Loros JJ, Dunlap JC
Citation(s) 36603054
NIH grant(s)
Grant ID Grant title Affiliation Name
F32 GM128252 Genetic and Molecular Dissection of Regulatory Mechanisms Underlying Temperature and Nutritional Compensation of the Circadian Clock in Neurospora crassa DARTMOUTH COLLEGE Christina Marie Kelliher
R35 GM118021 Genetic and Molecular Dissection of the Neurospora Clock DARTMOUTH COLLEGE Jay C. Dunlap
Submission date Apr 29, 2022
Last update date Feb 03, 2023
Contact name Christina M Kelliher
E-mail(s) Christina.M.Kelliher@dartmouth.edu
Organization name Geisel School of Medicine at Dartmouth
Department Molecular & Systems Biology
Street address 7400 Hinman
City Hanover
State/province NH
ZIP/Postal code 03755
Country USA
 
Platforms (1)
GPL32221 Illumina MiniSeq (Neurospora crassa)
Samples (4)
GSM6077761 1785-1_control_rep1
GSM6077762 2029_cpsf5cpsf6_rep1
GSM6077763 1785-1_control_rep2
Relations
BioProject PRJNA833430

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Supplementary file Size Download File type/resource
GSE201901_cpsf56_control_htseq_normalized.txt.gz 195.8 Kb (ftp)(http) TXT
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Raw data are available in SRA
Processed data are available on Series record

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