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Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration.

Clotilde Lagier-Tourenne, Michael Baughn, Frank Rigo, Shuying Sun, Patrick Liu, Hai-Ri Li, Jie Jiang, Andrew T Watt, Seung Chun, Melanie Katz, Jinsong Qiu, Ying Sun, Shuo-Chien Ling, Qiang Zhu, Magdalini Polymenidou, Kevin Drenner, Jonathan W Artates, Melissa McAlonis-Downes, Sebastian Markmiller, Kasey R Hutt, Donald P Pizzo, Janet Cady, Matthew B Harms, Robert H Baloh, Scott R Vandenberg, Gene W Yeo, Xiang-Dong Fu, C Frank Bennett, Don W Cleveland, John Ravits

Proceedings of the National Academy of Sciences of the United States of America · 2013 · Vol. 110 (47) · pp. E4530-9

Abstract

Expanded hexanucleotide repeats in the chromosome 9 open reading frame 72 (C9orf72) gene are the most common genetic cause of ALS and frontotemporal degeneration (FTD). Here, we identify nuclear RNA foci containing the hexanucleotide expansion (GGGGCC) in patient cells, including white blood cells, fibroblasts, glia, and multiple neuronal cell types (spinal motor, cortical, hippocampal, and cerebellar neurons). RNA foci are not present in sporadic ALS, familial ALS/FTD caused by other mutations (SOD1, TDP-43, or tau), Parkinson disease, or nonneurological controls. Antisense oligonucleotides (ASOs) are identified that reduce GGGGCC-containing nuclear foci without altering overall C9orf72 RNA levels. By contrast, siRNAs fail to reduce nuclear RNA foci despite marked reduction in overall C9orf72 RNAs. Sustained ASO-mediated lowering of C9orf72 RNAs throughout the CNS of mice is demonstrated to be well tolerated, producing no behavioral or pathological features characteristic of ALS/FTD and only limited RNA expression alterations. Genome-wide RNA profiling identifies an RNA signature in fibroblasts from patients with C9orf72 expansion. ASOs targeting sense strand repeat-containing RNAs do not correct this signature, a failure that may be explained, at least in part, by discovery of abundant RNA foci with C9orf72 repeats transcribed in the antisense (GGCCCC) direction, which are not affected by sense strand-targeting ASOs. Taken together, these findings support a therapeutic approach by ASO administration to reduce hexanucleotide repeat-containing RNAs and raise the potential importance of targeting expanded RNAs transcribed in both directions.

Linked datasets 3

GSE51685 GSE · via ncbi_elink
GEO ↗

Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for amyotrophic lateral sclerosis and frontotemporal dementia (strand specific RNA-seq)

Mus musculus

21 data files
FileTypeSize
MP100.fastq.gz RNA-Seq 7.4 GB
MP101.fastq.gz RNA-Seq 6.2 GB
MP102.fastq.gz RNA-Seq 6.1 GB
MP103.fastq.gz RNA-Seq 5.5 GB
MP107.fastq.gz RNA-Seq 6.9 GB
MP108.fastq.gz RNA-Seq 6.7 GB
MP109.fastq.gz RNA-Seq 7.3 GB
MP98.fastq.gz RNA-Seq 6.4 GB
MP99.fastq.gz RNA-Seq 6.1 GB
SRR1017123_GSM1251885 RNA-Seq 6.4 GB
SRR1017124 RNA-Seq 6.1 GB
SRR1017124_GSM1251886 RNA-Seq 6.1 GB
SRR1017125_GSM1251887 RNA-Seq 7.4 GB
SRR1017126_GSM1251888 RNA-Seq 6.2 GB
SRR1017127 RNA-Seq 6.1 GB
SRR1017127_GSM1251889 RNA-Seq 6.1 GB
SRR1017128 RNA-Seq 5.5 GB
SRR1017128_GSM1251890 RNA-Seq 5.5 GB
SRR1017129_GSM1251891 RNA-Seq 6.9 GB
SRR1017130_GSM1251892 RNA-Seq 6.7 GB
SRR1017131_GSM1251893 RNA-Seq 7.3 GB
GSE51741 GSE · via ncbi_elink
GEO ↗

Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for amyotrophic lateral sclerosis and frontotemporal dementia

Mus musculus

GSE51684 GSE · via ncbi_elink
GEO ↗

Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for amyotrophic lateral sclerosis and frontotemporal dementia (Multiplex Analysis of PolyA-linked Sequences)

Homo sapiens

54 data files
FileTypeSize
ALS14.fq.gz RNA-Seq 522.4 MB
ALS20.fq.gz RNA-Seq 495.2 MB
ALS25.fq.gz RNA-Seq 443.3 MB
ALS2.fq.gz RNA-Seq 543.8 MB
C9-1-Ctrl.fq.gz RNA-Seq 595.0 MB
C9-1-Mock.fq.gz RNA-Seq 734.8 MB
C9-1-Tx.fq.gz RNA-Seq 569.6 MB
C9-2-Ctrl.fq.gz RNA-Seq 558.8 MB
C9-2-Mock.fq.gz RNA-Seq 702.9 MB
C9-2-Tx.fq.gz RNA-Seq 762.7 MB
C9-3-Ctrl.fq.gz RNA-Seq 868.5 MB
C9-3-Mock.fq.gz RNA-Seq 509.1 MB
C9-3-Tx.fq.gz RNA-Seq 581.8 MB
C9-4-Ctrl.fq.gz RNA-Seq 628.0 MB
C9-4-Mock.fq.gz RNA-Seq 635.5 MB
C9-4-Tx.fq.gz RNA-Seq 605.7 MB
Kin1ALS17-Ctrl.fq.gz RNA-Seq 705.7 MB
Kin1ALS17-Tx.fq.gz RNA-Seq 697.5 MB
Kin1ALS6-Ctrl.fq.gz RNA-Seq 769.0 MB
Kin1ALS6-Tx.fq.gz RNA-Seq 752.5 MB
Kin2ALS6-Ctrl.fastq RNA-Seq 615.4 MB
Kin2ALS6-Tx.fq.gz RNA-Seq 568.5 MB
Kin4ALS6-Ctrl.fq.gz RNA-Seq 599.5 MB
Kin4ALS6-Tx.fq.gz RNA-Seq 892.6 MB
SRR1017149 RNA-Seq 522.4 MB
SRR1017149_GSM1250452 RNA-Seq 522.0 MB
SRR1017150_GSM1250453 RNA-Seq 495.0 MB
SRR1017151 RNA-Seq 443.3 MB
SRR1017151_GSM1250454 RNA-Seq 443.0 MB
SRR1017152_GSM1250455 RNA-Seq 543.0 MB
SRR1017153_GSM1250456 RNA-Seq 594.0 MB
SRR1017154_GSM1250457 RNA-Seq 734.0 MB
SRR1017155_GSM1250458 RNA-Seq 569.0 MB
SRR1017156_GSM1250459 RNA-Seq 558.0 MB
SRR1017157 RNA-Seq 702.9 MB
SRR1017157_GSM1250460 RNA-Seq 702.0 MB
SRR1017158 RNA-Seq 762.7 MB
SRR1017158_GSM1250461 RNA-Seq 762.0 MB
SRR1017159 RNA-Seq 868.5 MB
SRR1017159_GSM1250462 RNA-Seq 868.0 MB
SRR1017160 RNA-Seq 509.1 MB
SRR1017160_GSM1250463 RNA-Seq 509.0 MB
SRR1017161_GSM1250464 RNA-Seq 581.0 MB
SRR1017162_GSM1250465 RNA-Seq 628.0 MB
SRR1017163_GSM1250466 RNA-Seq 635.0 MB
SRR1017164_GSM1250467 RNA-Seq 605.0 MB
SRR1017165_GSM1250468 RNA-Seq 705.0 MB
SRR1017166_GSM1250469 RNA-Seq 697.0 MB
SRR1017167_GSM1250470 RNA-Seq 769.0 MB
SRR1017168_GSM1250471 RNA-Seq 752.0 MB
SRR1017169_GSM1250472 RNA-Seq 615.0 MB
SRR1017170_GSM1250473 RNA-Seq 568.0 MB
SRR1017171_GSM1250474 RNA-Seq 599.0 MB
SRR1017172_GSM1250475 RNA-Seq 892.0 MB

Analysis pipelines 3

Pipeline Assay Steps Dataset
GSE51684 Data Processing geo_data_processing — 4 GSE51684
GSE51685 RNA-seq Data Processing geo_data_processing RNA-seq 6 GSE51685
GSE51741 Data Processing geo_data_processing — 4 GSE51741
Funding 8 grants
Grant Funder
R01 NS075449 NINDS NIH HHS (United States)
T32 AG 000216 NIA NIH HHS (United States)
089701 Wellcome Trust (United Kingdom)
T32 AG000216 NIA NIH HHS (United States)
K08 NS075094 NINDS NIH HHS (United States)
K99 NS075216 NINDS NIH HHS (United States)
R01 NS088578 NINDS NIH HHS (United States)
K99NS075216 NINDS NIH HHS (United States)