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Sample GSM2141895 Query DataSets for GSM2141895
Status Public on Oct 19, 2016
Title TCS_lac_241
Sample type RNA
 
Source name Rats treated with triclosan from postnatal day 1 to 145
Organism Rattus norvegicus
Characteristics strain: Sprague-Dawley
Sex: Female
tissue: Caudal mammary tissue
exposure/treatment condition: Triclosan
window of exposure: Chronic
age at sacrifice: Rats sacrificed at postnatal day 146
batch: One
rna extraction kit: Promega
Treatment protocol Perinatal animals: five animals were treated in utero daily through oral gavage of their pregnant dams (F0) from gestation day (GD) 1 to GD 20; another five animals were treated daily from post natal day (PND)1 to PND 20 through milk of lactating dams (F0) exposed by oral gavage. One female pup per litter was randomly selected and sacrificed at PND 21. Prepubertal animals: treated daily from PND 21 through breast milk, then by oral gavage from PND 28 to PND 41, and sacrificed at PND 42. Pubertal animals: treated daily by oral gavage from PND 42 to PND 62, and sacrificed at PND 63. Chronic treatment group: animals were treated daily from PND 1 through milk of dams (F0) exposed from parturition. After weaning, the female offspring (F1) were treated through oral gavage 3 times a week. Animals were mated (outbred) at PND 97 and treatments were continued through pregnancy, delivery of pups (F2) and lactation. At the end of lactation at lactating day 28 (PND 146), F1 animals were sacrificed.
Growth protocol The breeder animals (F0) were weighed weekly to determine treatment dose, starting from gestation for the perinatal group and during lactation for prepubertal, pubertal, and adult groups and the dose to be administered was calculated on the basis of the weekly weight. For the perinatal group, all the F1 pups were housed with their dams until sacrifice (postnatal (PND) 21). F1 pups from all the other groups were housed with their dams (F0) until weaning (PND 28) then separated from the dam, identified by ear punch, weighed individually every week and dosed by gavage following the protocol, based on the weekly mean body weight of each group. Animals were randomized into different treatment groups in order to have minimal differences in body weight among them, with a standard deviation of no more than 10% from the average.
Extracted molecule total RNA
Extraction protocol The 5th left and right caudal mammary glands were used for transciptome profiling. Mammary tissues were pulverized in liquid nitrogen and total RNA was extracted using the Maxwell 16 LEV simplyRNA Blood kit (Promega, WI) or the Direct-zol RNA MiniPrep kit (Zymo Research, CA). Total RNA concentration was determined using Nanodrop (Thermo Scientific, MA), and RNA quality was assessed using a 2100 Bioanalyzer (Agilent Technologies, CA); only samples with RNA Integrity Number ≥ 7 were used for microarrays.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 250 ng total RNA (Manual Target Preparation for GeneChip® Whole Transcript (WT) Expression Arrays, Affymetrix 2015).
 
Hybridization protocol Following fragmentation, 5.2 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Rat Gene 2.0 St arrays. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Scan protocol Arrays were scanned using the GeneChip Scanner 3000.
Description Gene expression data from rat mammary tissues at postnatal day 146 following treatment with triclosan from postnatal day 1 to postnatal day 145
Data processing The data was preprocessed in Expression Console software (Affymetrix) using RMA-sketch workflow and default settings. Transcriptome results from MPB and TCS treatment during three short term windows – perinatal, prepubertal and pubertal windows – were pre-processed independently to generate two separate datasets (MPB and control - table 1, TCS and control - table 2). Transcriptome data from chronically exposed TCS animals and corresponding controls were pre-processed separately from short term data (Chronic TCS and control - table 3). Batch effects were removed using the ComBat package in R (Leek J. T. et al, 2012) for datasets in table 1 and table 2 (no batch covariate in table 3). Data submitted here have not been corrected for batch effects. Batch information is provided in the sample datasheet.
 
Submission date May 03, 2016
Last update date Oct 19, 2016
Contact name Kalpana Gopalakrishnan
E-mail(s) kalpana.gopalakrishnan@mssm.edu
Organization name Icahn School of Medicine at Mount Sinai
Street address 1428 Madison Avenue, Atran Building 03-02
City New York
State/province NY
ZIP/Postal code 10029
Country USA
 
Platform ID GPL17117
Series (1)
GSE72276 Mammary transcriptome of rats treated with low-dose environmental chemicals at critical developmental windows

Data table header descriptions
ID_REF
VALUE Log2 RMA signal

Data table
ID_REF VALUE
17610314 2.858165
17610327 2.793368
17610335 2.770036
17610342 2.76422
17610349 2.504646
17610356 3.850331
17610363 3.301709
17610368 4.792511
17610371 4.002759
17610394 3.859845
17610400 6.321786
17610410 8.598951
17610419 7.054546
17610432 8.153873
17610448 5.680389
17610457 4.16737
17610464 8.045379
17610500 6.907526
17610505 4.375912
17610523 7.599225

Total number of rows: 36685

Table truncated, full table size 640 Kbytes.




Supplementary file Size Download File type/resource
GSM2141895_TCS_lac_241.CEL.gz 8.7 Mb (ftp)(http) CEL
Processed data included within Sample table
Processed data are available on Series record

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