Hippocampus Illumina NOE (Oct08) RankInv beta modify this page

Accession number: GN214

    Summary:

Experimental data set: No restraint stress and a single ethanol injection (NOE). This data set provides data on the effects of acute ethanol on gene expression with stress associated with handling and an IP injection. Survival period X hours. Please copy text and style for other INFO pages and see Mike Miles INFO pages.

This data set entered by Arthur Centeno and Lu Lu, Oct 15, 2008. Please contact Dr. Lu Lu regarding these expression data at lulu@utmem.edu.

Note: This INFO file still in progress

EXPERIMENTAL DATA SET (Unpublished): This is one of five INIA companion data sets generated using the hippocampus of LXS strains and the Illumina Mouse 6.1 bead array. The data set labeled Hippocampus Illumina (May07) RankInv provides baseline control expression data with no treatment at all. This NOS data set consists of animals who received a single IP injection of saline (NOS = no restraint saline) without restraint stress. This saline injection group is intended to provide appropriate control for cases that received an IP injection of ethanol. The only experimental stressor in this NOS data set is that associated with handling and the IP saline injection. Survival period was 4 hours. The paradigm that was used in this set of studies by Lu Lu and colleagues is identical to that used by Dr. Michael Miles (see his experimental prefrontal cortex data in GeneNetwork for both LXS and BXD strains).

The hippocampus is highly susceptible to the effects of stress and glucocorticoid hormone action. ADD TEXT, rationale, and links.

Samples were processed using a total of 12 Illumina Sentrix Mouse 6.1 Bead arrays.

    About the strains used to generate this set of data:

The LXS genetic reference panel of recombinant inbred strains consists of just over 70 strains. The LXS strains in this data set were obtained from Dr. Beth Bennett and colleagues at the University of Colorado, Bolder. All of these strains are fully inbred, many well beyond the 25th filial (F) generation of inbreeding. All of these LXS strains have been genotyped at 13,377 SNPs.

    About the animals and tissue used to generate this set of data:

All animals were raised at the University of Colorado or at University of Memphis in SPF facilities. All mice were killed by cervical dislocation. Whole brain dissections were performed at UTHSC by Lu Lu and colleagues. Hippocampal samples were close to complete but are likely to include variable amounts of fimbira and choroid plexus. Samples may also include parts of the subiculum.

The bilateral hippocampus tissue from one naive adults mouse was used to generate RNA samples. All animals were sacrificed between 9 AM and 5 PM during the light phase. All RNA samples were extracted at UTHSC by Feng Jiao.

All animals used in this study were between 60 and 74 days of age (average of 67 days; see Table 1 below). All animals were sacrifice between 9 AM and 5 PM during the light phase.

Sample Processing: Samples were processed by Lu Lu and colleagues in the Illumina Core at UTHSC between April 2007 and November 2007. All processing steps were performed by Feng Jiao. In brief, RNA purity was evaluated using the 260/280 nm absorbance ratio, and values had to be greater than 1.8 to pass our quality control (QC). The majority of samples had values between 1.9 and 2.1. RNA integrity was assessed using the Agilent Bioanalyzer 2100. The standard Eberwine T7 polymerase method was used to catalyze the synthesis of cDNA template from polyA-tailed RNA using the Ambion/Illumina (http://www.ambion.com/catalog/CatNum.php?AMIL1791). TotalPrep RNA amplication kit (Cat#IL1791). The biotin labeled cRNA was then evaluated using both the 260/280 ratio (values of 2.0-2.3 are acceptable) using a NanoDrop ND-1000 (http://www.nanodrop.com/nd-1000-overview.html). Those samples that passed QC steps (1-3% failed and new RNA samples had to be acquired and processed) were immediately used on Mouse-6 v 1.1 slide. The slides were hybridized and washed following standard Illumina protocols.

Replication and Sample Balance: We obtained matched male and female sample from 27 strains. The following three strains are represented by male samples only: LXS25, 88, and 98. Three other strains, LXS19, 42, and 92 are represented only by female samples.

Legend:Sex balance of the NOE data set is revealed by expression of the Xist RNA (Illumina probe ILM1042800446). Male samples have low expression of Xist (about 7 units), whereas females have high expression (about 13 units). Each bar provides the mean expression value (log2 transformed) for a single strain. Strains with both male and female samples have intermediate averages and large error bars.

Experimental Design and Batch Structure: This data set consists arrays processed in 17 groups over a seven month period (from April 2007 to November 2007). Most groups consisted of 5 samples. All arrays in this data set were processed using a single protocol by a single operator, Feng Jiao. Processing was supervised directly by Dr. Lu Lu. All samples were scanned on a single Illumina Beadstation housed in the Hamilton Eye Institute between April 24, 2007 and November 20, 2007 . Details on sample assignment to slides and batches is provide in the table below.

Error checking

  • Checked for genotypes of LXS strains using a battery of test Mendelian transcripts (transcripts with a Mendelian segregation pattern in the LXS strains). Peak LRS of 201.7 for C1orf57 using Illumina probe ILM110129. There are no known errors in the strain assignment. (NOS data set)

    These genotype discrepancies are either due to recombination between the marker and the probe or a genotyping errors. (RWW, Feb 27, 2008)
  • Total count of transcripts/probes with LRS greater than 46 (LOD>10) is 754 with 31 LXS strains (NOS data set).

    NOE DATA AS OF Oct 2008: Data Table 1:

This table lists all arrays by order of strain (index) and includes data on tube ID, strain, age, sex, F generation number, number of animals in each sample pool (pool size), slide ID, slide position (A through F), scan date, and scan batch.

IndexTube IDStrainAgeSexPool SizeSlide IDSlide positionBatch by slidescan batch
1R3729HILS72M11736925158A146
2R3805HILS63F11825397033A2310
3R3884HISS66M11825397033B2310
4R3932HISS66F11870382129B5314
5R3941HLXS368F11736925148E1312
6R3717HLXS364M11736925162D156
7R3849HLXS365F11870382055D5014
8R3850HLXS363M11870382090E5115
9R3811HLXS773M11736925120E911
10R3768HLXS773F11825397032D2216
11R3767HLXS773F11825397077D3113
12R3886HLXS765F11825397111A3717
13R3711HLXS1469F11736925158E146
14R3939HLXS1469M11825397041B2610
15R3872HLXS1664M11825397041D2610
16R3732HLXS1672F11833451012D4118
17R3861HLXS1967F11825397041E2610
18R3678HLXS2365F11736925131A114
19R3679HLXS2364M11736925131B114
20R3802HLXS2365F11825397041F2610
21R4443LXS2370F11953348009F542
22R3752HLXS2570M11725572045B47
23R3751HLXS2570M11736925162C156
24R3808HLXS2674M11736925148D1312
25R3807HLXS2674F11825397042A2710
26R4455LXS3267F11848071018E471
27R4456LXS3267M11848071018F471
28R3818HLXS3670M11736925148F1312
29R3817HLXS3670F11825397042C2710
30R3755HLXS3967M11736925162E156
31R3683HLXS3966F11833451012B4118
32R4440LXS3969M11953348009E542
33R3701HLXS4269F11833451012E4118
34R3674HLXS4367F11736925130C104
35R3820HLXS4374M11825397042E2710
36R3877HLXS4664M11736925163C1612
37R3876HLXS4664F11825397042F2710
38R3795HLXS5066F11736925163D1612
39R3781HLXS5070M11825397077B3113
40R3866HLXS5167F11736925163E1612
41R3867HLXS5167M11825397073F2916
42R3919HLXS5473M11736925120C911
43R4463LXS5461F11848071023D483
44R3856HLXS6661F11735640066C715
45R3857HLXS6661M11825397080C3316
46R3763HLXS7870F11825397036E2516
47R3758HLXS7868M11848071016E5718
48R3838HLXS8064M11736925120F911
49R3901HLXS8066F11833451018D4317
50R3718HLXS8871M11736925164D176
51R3745HLXS8874M11825397020B219
52R3906HLXS9072M11735640066F715
53R3905HLXS9072F11870382102D5214
54R3702HLXS9272F11716756046D37
55R3724HLXS9771M11716756046E37
56R3911HLXS9770F11736925322C1911
57R3923HLXS9873M11735640068B815
58R3881HLXS9864M11736925322D1911
59R3813HLXS9975M11736925322E1911
60R3930HLXS9968F11825397081A3416
61R3748HLXS10075M11736925158B146
62R3787HLXS10066F11825397076B3013
63R3890HLXS10367F11735640068E815
64R3827HLXS10367M11736925146A1211
65R3831HLXS11064M11825397033E2310
66R3898HLXS11066F11833451017A4217
67R4452LXS11074M11953348032C562
68R3695HLXS12272M11725572051E65
69R3694HLXS12265M11725572051D65
70R3697HLXS12266F11736925158C146
71R3688HLXS12268M11833451008E394
72R3743HLXS12373M11714451029D18
73R3799HLXS12365M11736925146D1211
74R3710HLXS12365F11736925158D146
75R3798HLXS12365M11825397041A2610

    Downloading all data:

All data links (right-most column above) will be made active as soon as the global analysis of these data has been accepted for publication. Please see text on Data Sharing Policies, and Conditions and Limitations, and Contacts. Following publication, download a summary text file or Excel file of data. Please contact Lu Lu or RW Williams if you have questions about these data.

    About the array platform:

Illumina Sentrix Mouse-6.1 BeadArray Platform (ILM6v1.1): The Mouse6.1 array consists of 46,643 unique probe sequences, each 50 nucleotides in length, that have been arrayed on glass slides using a novel bead technology.

ANNOTATION: In summer of 2008, Xusheng Wang and Robert W. Williams reannotated the Illumina Mouse-6.1 array content. This new annotation is now incorporated into GeneNetwork. For 46643 probes on the Mouse 6.1 array platform (including control probes) we have identified 40183 NCBI Entrez Gene IDs; 22527 matched human Gene IDs; 11657 matched rat Gene IDs; 40983 NCBI HomoloGene IDs; and 22174 OMIM IDs.

Position data for the 50-mer Illumina Mouse-6 array were initially downloaded from Sanger at http://www.sanger.ac.uk/Users/avc/Illumina/Mouse-6_V1.gff.gz but we then updated all positions by BLAT analysis from mm6 positions to mm8 positions (Hongqiang Li).

    About data processing:

This data set uses the standard Rank Invariant method developed by Illumina and described in their BeadStation Studio documentation.

Sex of the samples was tested and validated using sex-specific probe set: Xist probe ILM104280446.

Legend: Checking that the sex of samples were labeled correctly was done using Xist expression measured by probe ILM106520068. In this bar chart the expression of Xist is very low in ILS and in six of the LXS strains: LXS43, 110, 54, 78, 39, and 25. This is because both arrays are male samples rather than 1 male and 1 female sample. In contrast LXS19 and LXS92 have very high expression. LXS19 data is from a single female pool (no error bar) whereas LXS92 is from tow female pools.

    Data source acknowledgment:

Data were generated with funds to Lu Lu from the NIAAA INIA program. Informatics support provided by NIH NIAAA INIA grants to RWW and LL.

  • Lu Lu, M.D.
    Grant Support: NIH U01AA13499, U24AA13513 (Lu Lu, PI)

  •     About this text file:

    This text files was initially entered by Robert W. Williams, Oct 20, 2008. The data set was entered by Arthur Centeno and Lu Lu, Oct 15, 2008. Please contact Dr. Lu Lu regarding these expression data at lulu@utmem.edu. Updated by Robert W. Williams, Oct 21, 2008. Updated by Lu Lu on Oct 22, 2008.