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SRX10853045: GSM5291269: Day_12_Control_4_R1; Homo sapiens; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 26.9M spots, 2.3G bases, 876.6Mb downloads

Submitted by: NCBI (GEO)
Study: Muscle group specific transcriptomic and DNA methylation differences related to developmental patterning influence FSHD [expression]
show Abstracthide Abstract
Muscle groups throughout the body are specialized in function and are specified during development by position specific gene regulatory networks. In developed tissue, myopathies affect muscle groups differently. Facioscapulohumeral muscular dystrophy, FSHD, affects upper body and tibialis anterior (TA) muscles earlier and more severely than others such as quadriceps. To investigate an epigenetic basis for susceptibility of certain muscle groups to disease, we perform DNA methylation and RNA sequencing on primary patient derived myoblasts from TA and quadricep for both control and FSHD2 as well as RNA-seq for myoblasts from FSHD1 deltoid, bicep and TA over a time course of differentiation. We find that TA and quadricep retain methylation and expression differences in transcription factors that are key to muscle group specification during embryogenesis. FSHD2 patients have differences in DNA methylation and expression related to SMCHD1 mutations and FGF signaling. Genes induced specifically in FSHD are more highly expressed in more commonly affected muscle groups. We find a set of genes that distinguish more susceptible muscle groups including developmental associated TFs and genes involved in WNT signaling. Adult muscle groups therefore retain transcriptional and DNA methylation differences associated with development, which may contribute to susceptibility in FSHD. Overall design: Time-course of primary FSHD2 myoblasts from tibialis anterior and quadricep, control myoblasts from tibialis anterior and quadricep, FSHD1 myoblasts from bicep, deltoid and tibialis anterior
Sample: Day_12_Control_4_R1
SAMN19114900 • SRS8949030 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Cells were lifted using trypsin. Total RNA was extracted by using the RNeasy kit (QIAGEN). RNA was converted to cDNA using the Smart-Seq 2 protocol (Picelli, et al., Nat. Protoc., 2014). Libraries were constructed with the Nextera DNA Library Prep Kit (Illumina) for days 0 to 5 for FSHD2-3. The Nextera DNA Flex Library Prep Kit (Illumina) was used for all other RNA-seq samples. Libraries were sequenced on the Illumina NextSeq500 with paired-end 43 bp reads to a depth of 5 to 40 million reads.
Experiment attributes:
GEO Accession: GSM5291269
Links:
Runs: 1 run, 26.9M spots, 2.3G bases, 876.6Mb
Run# of Spots# of BasesSizePublished
SRR1450707826,895,0212.3G876.6Mb2024-05-11

ID:
14435885

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