Interactions of LINE-1 ORF1p with proteins and chromatin suggest a role in neuronal physiology.
The 1 match
- [1] § Materials and Methods › ATAC sequencing and analysis ↔ bin/stats2multiqc.sh, lines 88–142 · score 0.67 · deepTools, peak calling, filtered, duplicates, Profiles, mapping
Paper
Loaded from Europe PMC by your browser, not stored by OSCR: doi.org · Europe PMC
The paper is loaded when this pane is shown.
The authors' code
Shell · 143 lines · 5 KB · CECILL-2.1 · 1 match
- #!/bin/bash
- function usage {
- echo -e "usage : stats2multiqc.sh -s SAMPLE_PLAN -d DESIGN -a ALIGNER [-p][-h]"
- echo -e "Use option -h|--help for more information"
- }
- function help {
- usage;
- echo
- echo "stat2multiqc.sh"
- echo "---------------"
- echo "OPTIONS"
- echo
- echo " -s SAMPLE_PLAN"
- echo " -d DESIGN"
- echo " -a ALIGNER"
- echo " [-p]: paired-end mode"
- echo " [-m]: Mitochondrial chromosome name"
- echo " [-h]: help"
- exit;
- }
- is_pe=0
- mito_name="chrM"
- while getopts "s:d:a:m:ph" OPT
- do
- case $OPT in
- s) splan=$OPTARG;;
- d) design=$OPTARG;;
- a) aligner=$OPTARG;;
- m) mito_name=$OPTARG;;
- p) is_pe=1;;
- h) help ;;
- \?)
- echo "Invalid option: -$OPTARG" >&2
- usage
- exit 1
- ;;
- :)
- echo "Option -$OPTARG requires an argument." >&2
- usage
- exit 1
- ;;
- esac
- done
- if [[ -z $splan ]]; then
- usage
- exit
- fi
- all_samples=$(awk -F, '{print $1}' $splan)
- echo -e "Sample_ID,Sample_name,Number_of_reads,Number_of_aligned_reads,Percent_of_aligned_reads,Number_of_mito,Percent_of_mito,Number_of_hq_mapped_reads,Percent_of_hq_mapped_reads,Number_of_lq_mapped_reads,Percent_of_lq_mapped_reads,Number_of_duplicates,Percent_of_duplicates,Number_of_usable_reads,Percent_of_usable_reads,TSS_enrichment,Fraction_of_reads_in_peaks" > mqc.stats
- for sample in $all_samples
- do
- #SAMPLE NAME
- sname=$(grep "$sample," $splan | awk -F, '{print $2}')
- #ALIGNMENT
- if [ $aligner == "bowtie2" ]; then
- nb_frag=$(grep "reads;" mapping/${sample}_bowtie2.log | sed 's/ .*//')
- if [[ $is_pe == 1 ]]; then
- nb_reads=$(( $nb_frag * 2 ))
- else
- nb_reads=$nb_frag
- fi
- elif [ $aligner == "bwa-mem" ]; then
- # bwa.log file is in reads number (not pairs)
- nb_reads=$(grep 'Total' mapping/${sample}_bwa.log | awk -F "\t" '{print $2}')
- if [[ $is_pe == 1 ]]; then
- nb_frag=$(( $nb_reads / 2 ))
- else
- nb_frag=$nb_reads
- fi
- tail -n +3 mapping/${sample}_bwa.log > mapping/${sample}_bwa.mqc
- elif [ $aligner == "star" ]; then
- nb_frag=$(grep "Number of input reads" mapping/${sample}Log.final.out | cut -d"|" -f 2 | sed -e 's/\t//g')
- if [[ $is_pe == 1 ]]; then
- nb_reads=$(( $nb_frag * 2 ))
- else
- nb_reads=$nb_frag
- fi
- fi
- #Mapping stats (always in reads - so must be converted for PE)
- #These statistics are calculated after spike cleaning but before filtering
- nb_mapped=$(awk -F, '$1=="Mapped"{print $2}' mapping/${sample}_mappingstats.mqc)
- nb_mapped_hq=$(awk -F, '$1=="HighQual"{print $2}' mapping/${sample}_mappingstats.mqc)
- nb_mapped_lq=$(awk -F, '$1=="LowQual"{print $2}' mapping/${sample}_mappingstats.mqc)
- perc_mapped=$(echo "${nb_mapped} ${nb_reads}" | awk ' { printf "%.*f",2,$1*100/$2 } ')
- perc_mapped_hq=$(echo "${nb_mapped_hq} ${nb_reads}" | awk ' { printf "%.*f",2,$1*100/$2 } ')
- perc_mapped_lq=$(echo "${nb_mapped_lq} ${nb_reads}" | awk ' { printf "%.*f",2,$1*100/$2 } ')
- ##MITO
- if [[ -e mapping/stats/${sample}_raw.idxstats ]]; then
- nb_mito=$(awk -v mt=${mito_name} '$1==mt{print $3}' mapping/stats/${sample}_raw.idxstats)
- perc_mito=$(echo "${nb_mito} ${nb_mapped}" | awk ' { printf "%.*f",2,$1*100/$2 } ')
- else
- nb_mito='NA'
- perc_mito='NA'
- fi
- #PICARD
- if [[ -e mapping/${sample}.MarkDuplicates.metrics.txt ]]; then
- nb_dups_pair=$(grep -a2 "## METRICS" mapping/${sample}.MarkDuplicates.metrics.txt | tail -1 | awk -F"\t" '{print $7}')
- nb_dups_single=$(grep -a2 "## METRICS" mapping/${sample}.MarkDuplicates.metrics.txt | tail -1 | awk -F"\t" '{print $6}')
- nb_dups_optical=$(grep -a2 "## METRICS" mapping/${sample}.MarkDuplicates.metrics.txt | tail -1 | awk -F"\t" '{print $8}')
- nb_dups=$(( $nb_dups_pair * 2 + $nb_dups_single + $nb_dups_optical ))
- perc_dups=$(echo "${nb_dups} ${nb_mapped}" | awk ' { printf "%.*f",2,$1*100/$2 } ')
- else
- nb_dups='NA'
- perc_dups='NA'
- fi
- #Filtered bam
- if [[ -e mapping/stats/${sample}_filtered.stats ]]; then
- nb_filt=$(grep ^SN mapping/stats/${sample}_filtered.stats | cut -f 2- | grep "reads mapped:" | cut -f 2)
- perc_filt=$(echo "${nb_filt} ${nb_mapped}" | awk ' { printf "%.*f",2,$1*100/$2 } ')
- fi
- #TSS Enrichment
- if [[ -e deepTools/${sample}_NFR.plotProfile_corrected.tab ]]; then
- tsse=$(awk -F"\t" 'NR==3{mn=mx=$3;for(i=3;i<=NF;i++){if($i>mx){mx=$i}};printf("%.*f",2, mx-mn)}' deepTools/${sample}_NFR.plotProfile_corrected.tab)
- else
- tsse='NA'
- fi
- #PeakCalling
- if [ -e peakCalling/${sample}_macs2_peaks.FRiP_mqc.tsv ]; then
- frip=$(grep "$sample" peakCalling/${sample}_macs2_peaks.FRiP_mqc.tsv | awk '{print $2}')
- elif [ -e peakCalling/${sample}_macs2_peaks.FRiP_mqc.tsv ]; then
- frip=$(grep "$sample" peakCalling/${sample}_genrich_peaks.FRiP_mqc.tsv | awk '{print $2}')
- else
- frip='NA'
- fi
- #To file
- echo -e ${sample},${sname},${nb_frag},${nb_mapped},${perc_mapped},${nb_mito},${perc_mito},${nb_mapped_hq},${perc_mapped_hq},${nb_mapped_lq},${perc_mapped_lq},${nb_dups},${perc_dups},${nb_filt},${perc_filt},${tsse},${frip} >> mqc.stats
- done
stats2multiqc.sh at commit 1b162c1, under CECILL-2.1 · at the source
Overview
- CIRB, Collège de France, Université PSL, INSERM, CNRS, Paris, France
- Institut Curie, Université PSL, CurieCoreTech Mass Spectrometry Proteomics, Paris, France
- Orion Technological Core, CIRB, Collège de France, Université PSL, INSERM, CNRS, Paris, France
- Institut Curie, INSERM U900, Mines Paris Tech, Université PSL, Paris, France
Abstract
Retrotransposons are emerging as novel regulators of embryonic and brain development. We recently demonstrated that the LINE-1–encoded protein ORF1p is abundantly expressed in adult mouse and human neurons, although its function remains unclear. Here, we characterize the ORF1p interactome in differentiated mouse and human neurons using mass spectrometry and identify novel partners implicated in gene regulation and neuron-specific processes. ORF1p localizes not only to neuronal nuclei, where it associates with chromatin under steady-state conditions, but also to neurites, supporting a role in neuronal physiology. To further explore its nuclear functions, we sorted human post-mortem neurons with high or low nuclear ORF1p levels and performed ORF1p knockdown in cultured human neurons, followed by chromatin accessibility assays. Both approaches revealed consistent patterns of differential chromatin accessibility dependent on ORF1p. Loss of ORF1p also led to the down-regulation of long, neuron-specific genes and altered neurite morphology. Together, these findings point to a physiological role of ORF1p in post-mitotic neurons, mediated through converging interactions with proteins and chromatin.
Reproduced under the paper's license (CC BY), from the paper cited above.
Repositories
Its files are read in the Code ↔ Paper reader above, with 1 match between paragraphs and lines of code.
orion-cirb/Axon_Skel_Analyzer
debbd7ca96c6e73d8a48c6c3ae0d404190f3490f, 22 May 2025Availability: 1 check, the latest on 27 September 2026: the link answers
- 27 September 2026: the link answers
1 file, not copied: shown from their source
OSCR keeps no copy of these files: this repository has no license that allows it. The reader above shows each one from its source, fetched by your browser at commit debbd7c, when its fingerprint is the one OSCR verified. How this works.
- README.md — Text, 61 lines, shown from its source
bioinfo-pf-curie/atac-seq
1b162c12d313677f8836c657adc3d8ec74c0e94d, 22 October 2021Availability: 1 check, the latest on 27 September 2026: the link answers
- 27 September 2026: the link answers
12 files
- bin/
checkDesign.py — Python, 255 lines - bin/
getBWAstats.sh — Shell, 79 lines - bin/
markdown_to_html.py — Python, 100 lines - bin/
mqc_header.py — Python, 125 lines - bin/
plot_homer_annotatepeaks — R, 162 lines.r - bin/
plot_macs_qc.r — R, 156 lines - bin/
replicate_idr.py — Python, 62 lines - bin/
scrape_software_versions — Python, 62 lines.py - bin/
select_peakfiles_for_IDR — Python, 51 lines.py - bin/
stats2multiqc.sh — Shell, 143 lines, 1 match - LICENSE — License, 517 lines
- README.md — Text, 196 lines
Tracing map
Proposed by the machine: these links were found in the paper and verified at the source, without human review. The map will receive a Zenodo DOI once one of the paper's authors has validated it with their ORCID.
What the map holds:
- 2 repositories of the authors' code, each at its verified commit, with its license and how the link was found in the paper;
- 10 scripts, each with its path and the digest of its content;
- 1 match between paragraphs of the paper and lines of the code (method lexical-v1);
- neither the text of the paper nor the code itself.
Its JSON (tracing-map.json) is deposited on Zenodo with its DOI once the map is validated.
Data
Datasets cited
- alphafold.ebi.ac.uk/
entry/ — at EMBL-EBI; found in the text, “Identification of protein partners of…”af-p11260-f1 - alphafold.ebi.ac.uk/
entry/ — at EMBL-EBI; found in the text, “Identification of protein partners of…”q9un81 - arrayexpress:E-MTAB-1587
1 — at ArrayExpress; found in “Data Availability” - uniprot.org/
proteomes/ — at UniProt; found in the text, “LC-MS/MS analysis”up000000589
Data Availability
The ATAC-seq and RNA-seq data stemming from human differentiated neurons in culture (LUHMES) are available at EBI-EMBL ArrayExpress database under the following accession numbers: ATAC-seq: E- (https://
The mass spectrometry raw data are available on the PRIDE database with the accession number PXD066047 (https://
Reproduced under the paper's license (CC BY), from the paper cited above.
Versions
The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.
Version 1, 27 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 11 authors, 11 MeSH terms, 6 funders, 104 references.
Cite
This paper
Sinnassamy, S., Massiani Beaudoin, O., Lombard, B., Loew, D., Bonnifet, T., Fradet, M., Monnet, H., Caille, T., Servant, N., Joshi, R. L., & Fuchs, J. (2026). Interactions of LINE-1 ORF1p with proteins and chromatin suggest a role in neuronal physiology. Life science alliance, 9(11), e202503546. https://
BibTeX
@article{sinnassamy2026i
author = {Sinnassamy, Sandra and Massiani Beaudoin, Olivia and Lombard, Berangère and Loew, Damarys and Bonnifet, Tom and Fradet, Magali and Monnet, Héloïse and Caille, Thomas and Servant, Nicolas and Joshi, Rajiv L and Fuchs, Julia},
title = {{Interactions of LINE-1 ORF1p with proteins and chromatin suggest a role in neuronal physiology}},
journal = {Life science alliance},
year = {2026},
month = aug,
volume = {9},
number = {11},
pages = {e202503546},
publisher = {Life Science Alliance LLC},
issn = {2575-1077},
doi = {10.26508/
url = {https://
pmid = {42629196},
pmcid = {PMC13498733}
}
RIS
TY - JOUR
AU - Sinnassamy, Sandra
AU - Massiani Beaudoin, Olivia
AU - Lombard, Berangère
AU - Loew, Damarys
AU - Bonnifet, Tom
AU - Fradet, Magali
AU - Monnet, Héloïse
AU - Caille, Thomas
AU - Servant, Nicolas
AU - Joshi, Rajiv L
AU - Fuchs, Julia
TI - Interactions of LINE-1 ORF1p with proteins and chromatin suggest a role in neuronal physiology
T2 - Life science alliance
J2 - Life Sci Alliance
PY - 2026
DA - 2026/
VL - 9
IS - 11
SP - e202503546
SN - 2575-1077
PB - Life Science Alliance LLC
DO - 10.26508/
UR - https://
LA - en
ER -
CSL-JSON
{
"id": "10.26508/
"type": "article-journal",
"title": "Interactions of LINE-1 ORF1p with proteins and chromatin suggest a role in neuronal physiology",
"container-title": "Life science alliance",
"author": [
{
"family": "Sinnassamy",
"given": "Sandra"
},
{
"family": "Massiani Beaudoin",
"given": "Olivia"
},
{
"family": "Lombard",
"given": "Berangère"
},
{
"family": "Loew",
"given": "Damarys"
},
{
"family": "Bonnifet",
"given": "Tom"
},
{
"family": "Fradet",
"given": "Magali"
},
{
"family": "Monnet",
"given": "Héloïse"
},
{
"family": "Caille",
"given": "Thomas"
},
{
"family": "Servant",
"given": "Nicolas"
},
{
"family": "Joshi",
"given": "Rajiv L"
},
{
"family": "Fuchs",
"given": "Julia"
}
],
"container-title-short":
"volume": "9",
"issue": "11",
"page": "e202503546",
"DOI": "10.26508/
"PMID": "42629196",
"PMCID": "PMC13498733",
"ISSN": "2575-1077",
"publisher": "Life Science Alliance LLC",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
[
2026,
8,
21
]
]
}
}
The tracing map gets a citation of its own once an author has validated it and it has a DOI.
Similar papers
The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.
- [1] doi:10.1002/jdn.70161 [code]
- Spatio-Temporal Dynamics of Macroglial Cell Organization and Proximity to Blood Vessels During Postnatal Development.Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental NeuroscienceIn common: pandas, NumPy, mouse, 3 references, author Héloïse Monnet
- [2] doi:10.1186/s13059-026-04177-w [code]
- Genomic sequence evolution underlying human neocortical interareal diversification.Journal: Genome biologyIn common: SAMtools, reshape2, ggplot2, 2 other tools, mouse, cellular / molecular, 2 references
- [3] doi:10.1126/sciadv.aed2952 [code]
- Activation of transposable elements is linked to a region- and cell type-specific interferon response in Parkinson's disease.Journal: Science advancesIn common: SAMtools, reshape2, ggplot2, 2 other tools, cellular / molecular, 2 references
- [4] doi:10.1038/s41586-026-10612-6 [code]
- Acquired genetic and cell-state changes in IDH-mutant glioma progression.Journal: NatureIn common: SAMtools, reshape2, ggplot2, 2 other tools, cellular / molecular, 1 reference
- [5] doi:10.1038/s41467-026-73325-4 [code]
- A scalable Tn5-based method for genome-wide DNA methylation profiling in development and disease.Journal: Nature communicationsIn common: SAMtools, reshape2, ggplot2, 2 other tools, 1 reference
- [6] doi:10.1038/s42003-026-10957-8 [code]
- Brain defence by the extracellular matrix protein Cochlin.Journal: Communications biologyIn common: SAMtools, reshape2, ggplot2, 2 other tools, mouse, cellular / molecular
- [7] doi:10.1038/s41467-026-73796-5 [code]
- Cross-species transcriptomic analysis of rodent model fidelity to human mesial temporal lobe epilepsy.Journal: Nature communicationsIn common: SAMtools, reshape2, ggplot2, 2 other tools, mouse, cellular / molecular
- [8] doi:10.1038/s41467-026-73305-8 [code]
- Comparative analysis of the cellular landscape in mammalian striatum.Journal: Nature communicationsIn common: SAMtools, reshape2, ggplot2, 2 other tools, mouse, cellular / molecular
- [9] doi:10.1038/s41586-026-10512-9 [code]
- Astrocyte glucocorticoid receptor signalling restricts neuronal plasticity.Journal: NatureIn common: SAMtools, reshape2, ggplot2, 2 other tools, mouse, cellular / molecular
- [10] doi:10.3389/fnmol.2026.1844705 [code]
- Risperidone regulates the expression of schizophrenia-related genes in the forebrain of adult male mice.Journal: Frontiers in molecular neuroscienceIn common: SAMtools, reshape2, ggplot2, 2 other tools, mouse, cellular / molecular
Contribute
The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.
Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.
Claim this paper
Correct its record
Say what each link of this record is, remove the ones that are not the paper's, add the ones that are missing. The correction becomes a new version of the record, in its Versions section.
Validate its tracing map
You validate the map as this page shows it: 2 repositories of the authors' code, each at its verified commit and with its license, 10 scripts, and 1 match between paragraphs and code (see the Code and Map sections). It then receives a DOI on Zenodo, with you (your ORCID iD) and OSCR as its creators; the code itself is not deposited.
The map's fingerprint: sha256:0226502b92790cb1…
Add the badge to its README
The badge links the code to this page. Copy one of these into the README of the paper's code: only you decide where it goes, and nothing is changed for you.
Markdown
[, paste the snippet at the top, then “Commit changes…” and, to review it first, “Create a new branch and start a pull request”. You open the pull request; OSCR asks for no permission.
Request its removal
To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).
Discussion, reproductions, activity
Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.
Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.
Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.
