OSCR

Proteomic profile of hippocampal growth cones through early postnatal development.

Code ↔ Paper

13 matches between paragraphs of the paper and lines of its authors' code, computed by the harvester (lexical-v1). Click a colored paragraph or line to see its counterpart.

The 13 matches · 1 of them tie a paragraph to a whole file without given lines: a weak match, whose lines are not tinted
  1. [1] § RESULTS › Growth cones of the DG in early postnatal days ↔ Proteomics/scripts/part3_GO_analysis.R, lines 89 to 149 · score 0.99 · Golgi vesicle transport, Protein DNA complex, RNA catabolic processes, Mitochondrial gene expression, tRNA, RNA metabolism · Report a mismatch
  2. [2] § RESULTS › Time-regulated proteins associated with neurological disorders ↔ Proteomics/scripts/part5_disease_terms.R, lines 1 to 62 · score 0.93 · Amyotrophic lateral sclerosis, autism spectrum disorders, epilepsy syndrome, neurological diseases, neurological disorders, regulated proteins · Report a mismatch
  3. [3] § RESULTS › Hippocampal growth cones in early postnatal days ↔ Proteomics/scripts/part3_GO_analysis.R, lines 89 to 149 · score 0.85 · Immunoglobulin mediated immune, RNA catabolic processes, RNA splicing, mRNA, GO, cell · Report a mismatch
  4. [4] § MATERIALS AND METHODS › Proteomic data analysis ↔ Proteomics/scripts/part1_raw_data_processing.R, lines 1 to 76 · score 0.80 · MaxQuant, potential contaminants, LFQ intensity, raw, reverse, match · Report a mismatch
  5. [5] § MATERIALS AND METHODS › Confocal imaging and growth cones count ↔ Fluorescent image analysis/main.m, lines 115 to 154 · score 0.75 · CA3 SLM, inner blade, outer blade, Stx7, ML, GFP · Report a mismatch
  6. [6] § RESULTS › Hippocampal growth cones in early postnatal days ↔ Proteomics/scripts/part1_raw_data_processing.R, lines 1 to 76 · score 0.74 · log2 LFQ intensities, log2 transformed, MaxQuant, Raw, contaminations, isolating · Report a mismatch
  7. [7] § MATERIALS AND METHODS › Proteomic data analysis ↔ Proteomics/scripts/part2_basic_characterisation.R, lines 85 to 152 · score 0.74 · ShinyGO, KEGG pathway, Disease terms, FDR, genes, proteome · Report a mismatch
  8. [8] § MATERIALS AND METHODS › Confocal imaging and growth cones count ↔ Fluorescent image analysis/FigureTools/dataIntegratorCounts.m, the whole file · a weak match · score 0.70 · delineated area, picture, mask, Volume, contours, GFP · Report a mismatch
  9. [9] § RESULTS › Characterization of the critical time window for early postnatal development in the hippocampus ↔ Fluorescent image analysis/main.m, lines 115 to 154 · score 0.67 · CA3 SLM, inner blade, outer blade, Stx7, GFP, fluorescent · Report a mismatch
  10. [10] § RESULTS › Subregion specificity of HP-GCs and DG-GCs ↔ Proteomics/scripts/part3_GO_analysis.R, lines 1 to 87 · score 0.66 · GO term, P3 HP, P1 HP, P5 DG, Uniprot, exploratory · Report a mismatch
  11. [11] § RESULTS › Characterization of the critical time window for early postnatal development in the hippocampus ↔ Fluorescent image analysis/main.m, lines 67 to 113 · score 0.62 · normalized volume, inner blade, outer blade, quartile, ML, threshold · Report a mismatch
  12. [12] § RESULTS › Growth cones of the DG in early postnatal days ↔ Proteomics/scripts/part2_basic_characterisation.R, lines 85 to 152 · score 0.62 · KEGG pathway, DG GC, HP GC, cardiomyocytes, overlap, proteomic · Report a mismatch
  13. [13] § RESULTS › Subregion specificity of HP-GCs and DG-GCs ↔ Proteomics/scripts/part2_basic_characterisation.R, lines 198 to 267 · score 0.61 · DG P5, P3 HP, P1 HP, Uniprot, Upset, overlap · Report a mismatch

Paper

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The authors' code

R · 186 lines · 9 KB · MIT · 3 matches

  1. library(clusterProfiler)
  2. library(org.Mm.eg.db)
  3. # ensure that you have generated the lists of exclusive proteins (s. part2 line 170 and following)
  4. #### GO term analysis for exclusive protein lists #####
  5. # results for enrichGO are thresholded on the given cutoff values. Only terms that pass both cutoffs are included.
  6. # For an exploratory approach no cutoffs are used in the following analysis to get a better understanding for the dataset.
  7. # pvalue and qvalueCutoff = 1
  8. P1_HP_excl_GO <- enrichGO(gene = P1_HP_exclusive,
  9. OrgDb = org.Mm.eg.db,
  10. keyType = "UNIPROT",
  11. ont = "BP",
  12. pvalueCutoff = 1,
  13. qvalueCutoff = 1,
  14. readable = TRUE)
  15. P1_HP_excl_GO_plot <- dotplot(P1_HP_excl_GO, showCategory = 20) +
  16. ggtitle("P1_HP exclusive") +
  17. theme(plot.title = element_text(hjust = 0.5, face = "bold"))
  18. P1_HP_excl_GO_plot
  19. # ggsave(paste(version, sep = "_", "P1_HP_excl_GO_plot.svg"), plot = P1_HP_excl_GO_plot, device = "svg", unit = "cm", height = 20, width = 17)
  20. P1_DG_excl_GO <- enrichGO(gene = P1_DG_exclusive,
  21. OrgDb = org.Mm.eg.db,
  22. keyType = "UNIPROT",
  23. ont = "BP",
  24. pvalueCutoff = 1,
  25. qvalueCutoff = 1,
  26. readable = TRUE)
  27. P1_DG_excl_GO_plot <- dotplot(P1_DG_excl_GO, showCategory = 20) +
  28. ggtitle("P1_DG exclusive") +
  29. theme(plot.title = element_text(hjust = 0.5, face = "bold"))
  30. P1_DG_excl_GO_plot
  31. # ggsave(paste(version, sep = "_", "P1_DG_excl_GO_plot.svg"), plot = P1_DG_excl_GO_plot, device = "svg", unit = "cm", height = 20, width = 17)
  32. P3_HP_excl_GO <- enrichGO(gene = P3_HP_exclusive,
  33. OrgDb = org.Mm.eg.db,
  34. keyType = "UNIPROT",
  35. ont = "BP",
  36. pvalueCutoff = 1,
  37. qvalueCutoff = 1,
  38. readable = TRUE)
  39. P3_HP_excl_GO_plot <- dotplot(P3_HP_excl_GO, showCategory = 20) +
  40. ggtitle("P3_HP exclusive") +
  41. theme(plot.title = element_text(hjust = 0.5, face = "bold"))
  42. P3_HP_excl_GO_plot
  43. # ggsave(paste(version, sep = "_", "P3_HP_excl_GO_plot.svg"), plot = P3_HP_excl_GO_plot, device = "svg", unit = "cm", height = 20, width = 17)
  44. P3_DG_excl_GO <- enrichGO(gene = P3_DG_exclusive,
  45. OrgDb = org.Mm.eg.db,
  46. keyType = "UNIPROT",
  47. ont = "BP",
  48. pvalueCutoff = 1,
  49. qvalueCutoff = 1,
  50. readable = TRUE)
  51. P3_DG_excl_GO_plot <- dotplot(P3_DG_excl_GO, showCategory = 20) +
  52. ggtitle("P3_DG exclusive") +
  53. theme(plot.title = element_text(hjust = 0.5, face = "bold"))
  54. P3_DG_excl_GO_plot
  55. # ggsave(paste(version, sep = "_", "P3_DG_excl_GO_plot.svg"), plot = P3_DG_excl_GO_plot, device = "svg", unit = "cm", height = 20, width = 17)
  56. P5_HP_excl_GO <- enrichGO(gene = P5_HP_exclusive,
  57. OrgDb = org.Mm.eg.db,
  58. keyType = "UNIPROT",
  59. ont = "BP",
  60. pvalueCutoff = 1,
  61. qvalueCutoff = 1,
  62. readable = TRUE)
  63. P5_HP_excl_GO_plot <- dotplot(P5_HP_excl_GO, showCategory = 20) +
  64. ggtitle("P5_HP exclusive") +
  65. theme(plot.title = element_text(hjust = 0.5, face = "bold"))
  66. P5_HP_excl_GO_plot
  67. # ggsave(paste(version, sep = "_", "P5_HP_excl_GO_plot.svg"), plot = P5_HP_excl_GO_plot, device = "svg", unit = "cm", height = 20, width = 17)
  68. P5_DG_excl_GO <- enrichGO(gene = P5_DG_exclusive,
  69. OrgDb = org.Mm.eg.db,
  70. keyType = "UNIPROT",
  71. ont = "BP",
  72. pvalueCutoff = 1,
  73. qvalueCutoff = 1,
  74. readable = TRUE)
  75. P5_DG_excl_GO_plot <- dotplot(P5_DG_excl_GO, showCategory = 20) +
  76. ggtitle("P5_DG exclusive") +
  77. theme(plot.title = element_text(hjust = 0.5, face = "bold"))
  78. P5_DG_excl_GO_plot
  79. # ggsave(paste(version, sep = "_", "P5_DG_excl_GO_plot.svg"), plot = P5_DG_excl_GO_plot, device = "svg", unit = "cm", height = 20, width = 17)
  80. # generate data frame with top hits based on the dotplot from all GO analyses
  81. df.P1_HP_excl_BP <- P1_HP_excl_GO_plot$data %>%
  82. mutate(Sample = "P1_HP")
  83. df.P1_DG_excl_BP <- P1_DG_excl_GO_plot$data %>%
  84. mutate(Sample = "P1_DG")
  85. df.P3_HP_excl_BP <- P3_HP_excl_GO_plot$data %>%
  86. mutate(Sample = "P3_HP")
  87. df.P3_DG_excl_BP <- P3_DG_excl_GO_plot$data %>%
  88. mutate(Sample = "P3_DG")
  89. df.P5_HP_excl_BP <- P5_HP_excl_GO_plot$data %>%
  90. mutate(Sample = "P5_HP")
  91. df.P5_DG_excl_BP <- P5_DG_excl_GO_plot$data %>%
  92. mutate(Sample = "P5_DG")
  93. df.Excl_HP_BP_Top20 <- full_join(df.P1_HP_excl_BP, df.P3_HP_excl_BP) %>%
  94. full_join(df.P5_HP_excl_BP)
  95. df.Excl_DG_BP_Top20 <- full_join(df.P1_DG_excl_BP, df.P3_DG_excl_BP) %>%
  96. full_join(df.P5_DG_excl_BP)
  97. HP_Top5 <- c("cellular amino acid metabolic process", "mitochondrial gene expression",
  98. "mitochondrial respiratory chain complex assembly", "organic acid catabolic process",
  99. "tRNA metabolic process",
  100. "mRNA splicing, via spliceosome", "RNA catabolic process", "regulation of cellular protein catabolic process",
  101. "regulation of mRNA stability", "regulation of mRNA processing",
  102. "immunoglobulin mediated immune response", "N-acetylneuraminate metabolic process",
  103. "water-soluble vitamin metabolic process", "sperm-egg recognition",
  104. "transcription initiation from RNA polymerase III promoter")
  105. df.Excl_HP_BP_Top5 <- df.Excl_HP_BP_Top20 %>%
  106. filter(Description %in% HP_Top5)
  107. # add vector with curated terms and filter df accordingly make plots here and compare to paper
  108. Excl_BP_HP_plot <- ggplot(df.Excl_HP_BP_Top5, aes(x = GeneRatio, y = Description, size = Count, color = p.adjust)) +
  109. geom_point() +
  110. scale_size(range = c(1, 5), name = "Count") +
  111. scale_color_gradient(low = "#509e97", high = "grey60", name = "p.adjust") +
  112. facet_grid(rows = vars(Sample), scales = "free") +
  113. theme_minimal() +
  114. theme(strip.background = element_rect(color = "grey90", fill="grey90"))
  115. Excl_BP_HP_plot
  116. # ggsave(paste(version, sep = "_", "Excl_BP_HP.svg"), plot = Excl_BP_HP_plot, device = "svg")
  117. DG_Top5 <- c( "mitochondrial gene expression", "cellular amino acid metabolic process",
  118. "sulfur compound metabolic process", "energy derivation by oxidation of organic compounds",
  119. "mitochondrial respiratory chain complex assembly",
  120. "RNA catabolic process", "positive regulation of cell cycle process",
  121. "protein-DNA complex subunit organization", "rRNA metabolic process",
  122. "nucleus organization",
  123. "positive regulation of neuron projection development", "Golgi vesicle transport",
  124. "mRNA splicing, via spliceosome", "vacuole organization", "dendrite morphogenesis")
  125. df.Excl_DG_BP_Top5 <- df.Excl_DG_BP_Top20 %>%
  126. filter(Description %in% DG_Top5)
  127. Excl_BP_DG_plot <- ggplot(df.Excl_DG_BP_Top5, aes(x = GeneRatio, y = Description, size = Count, color = p.adjust)) +
  128. geom_point() +
  129. scale_size(range = c(1, 5), name = "Count") +
  130. scale_color_gradient(low = "#d62f38", high = "grey60", name = "p.adjust") +
  131. facet_grid(rows = vars(Sample), scales = "free") +
  132. theme_minimal() +
  133. theme(strip.background = element_rect(color = "grey90", fill="grey90"))
  134. Excl_BP_DG_plot
  135. # ggsave(paste(version, sep = "_", "Excl_BP_DG.svg"), plot = Excl_BP_DG_plot, device = "svg")
  136. # Comparison of GO terms between timepoint specific proteins
  137. # make one data frame of GO results for timepoint specific proteins
  138. df.HP_P1_BP <- as.data.frame(P1_HP_excl_GO)
  139. df.HP_P1_BP$condition <- "P1-HP"
  140. df.HP_P3_BP <- as.data.frame(P3_HP_excl_GO)
  141. df.HP_P3_BP$condition <- "P3-HP"
  142. df.HP_P5_BP <- as.data.frame(P5_HP_excl_GO)
  143. df.HP_P5_BP$condition <- "P5-HP"
  144. df.DG_P1_BP <- as.data.frame(P1_DG_excl_GO)
  145. df.DG_P1_BP$condition <- "P1-DG"
  146. df.DG_P3_BP <- as.data.frame(P3_DG_excl_GO)
  147. df.DG_P3_BP$condition <- "P3-DG"
  148. df.DG_P5_BP <- as.data.frame(P5_DG_excl_GO)
  149. df.DG_P5_BP$condition <- "P5-DG"
  150. All_BP <- rbind(df.HP_P1_BP, df.HP_P3_BP, df.HP_P5_BP,
  151. df.DG_P1_BP, df.DG_P3_BP, df.DG_P5_BP)
  152. # extract all results of GO analysis for Top terms for HP and DG
  153. TOP_GO <- unique(c(HP_Top5, DG_Top5))
  154. Top5_BP_plot <- All_BP[All_BP$Description %in% TOP_GO,]
  155. Top_BP_plot <- ggplot(Top5_BP_plot, aes(x = condition, y = Description, size = Count, color = p.adjust)) +
  156. geom_point() +
  157. scale_size(range = c(2, 10), name = "Count") + # Adjust size scale
  158. scale_color_gradient(low = "darkred", high = "orange", name = "p.adjust") + # Color scale for p.adjust
  159. theme_minimal() +
  160. labs(x = NULL, y = NULL)
  161. Top_BP_plot
  162. # ggsave(paste(version, sep = "_", "TOP_BP.svg"), plot = Top_BP_plot, device = "svg")

part3_GO_analysis.R at commit 7d0a610, under MIT · at the source

Overview

Authors: Maike Krause1,2, Kamilla Aase Kronberg1, Paulo J B Girão1, Lara Sophie Strohmeier1, Giulia Quattrocolo1,2
  1. Kavli Institute for Systems Neuroscience and Centre for Algorithms of the Cortex, Norwegian University of Science and Technology (NTNU), 7491 Trondheim, Norway
  2. Mohn Research Center for the Brain, Norwegian University of Science and Technology (NTNU), 7491 Trondheim, Norway
Journal: Development (Cambridge, England), volume 153, issue 12, article dev205342
Dates: received 3 November 2025; accepted 25 May 2026; published online 22 June 2026; in print June 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1242/dev.205342 · PMID 42252990 · PMCID PMC13354955 · OpenAlex W4416109154
Open access: hybrid, a free copy (OpenAlex)
Status: code verified (how the code is found and verified)
Categories: genetics / omics (modality), mouse (organism), developmental (subfield)
Methods: Statistics, Evoked potentials
Keywords: Early postnatal development, Mouse, Growth cones, Proteomics, Local translation, Hippocampus
MeSH: Growth Cones*, Hippocampus*, Proteome*, Proteomics*, Animals, Dentate Gyrus, Mice, Mice, Inbred C57BL, Neurodevelopment (* major topic)
Topic: Neurogenesis and neuroplasticity mechanisms (Developmental Neuroscience, Neuroscience), according to OpenAlex
Funding: Kavli Foundation; Norges forskningsrad (332640, 223262, 324305); Norwegian University of Science and Technology; Norges Teknisk-Naturvitenskapelige Universitet (295721); Trond Mohn stiftelse (2021TMT04); Norges Forskningsråd (223262, 324305, 332640)
Citations: not cited yet (Europe PMC); 106 references in the paper

Abstract

Axonal growth cones rely on local proteomic changes to interpret guidance cues while navigating towards their synaptic targets. Yet the developmental dynamics of their proteome remain poorly understood. By isolating growth cones from the whole mouse hippocampus and dentate gyrus at early postnatal days, we performed a systematic characterization of their proteome. We show that growth cones from both subregions share a proteomic signature at postnatal day (P) 1, dominated by energy metabolism and protein synthesis, before taking distinct developmental trajectories. In fact, hippocampal growth cones undergo a rapid transition, from RNA-related processes to synapse formation. Dentate gyrus growth cones, however, maintain a similar proteomic profile at P3 and P5, suggesting a prolonged exploratory behaviour, consistent with later ingrowth of entorhinal cortex fibres. At these early timepoints, hippocampal and dentate gyrus growth cones are characterized by several temporally regulated proteins, suggesting dynamic and different developmental trajectories. Our dataset provides a comprehensive proteomic resource for understanding growth cone function during hippocampal circuit formation and insights into the molecular mechanisms underlying region-specific developmental timelines.

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 13 matches between paragraphs and lines of code.

Quattrocolo-Lab/krause-et-al-2026

License: MIT
State: the link answers, verified on 27 September 2026
Evidence: files inventoried
Commit: 7d0a61090d1642f2a4d7c830a3fc0ad964d37970, 7 April 2026
Languages: MATLAB (23), R (5)
Size: 33 files, 28 scripts
Software Heritage: not archived
Found in: the text, “Proteomic data analysis”
Holds: README, license file
Not found: CITATION.cff, environment file, tests, continuous integration, documentation
Tools: tidyverse (4 files), circlize (1 file), clusterProfiler (1 file), ComplexHeatmap (1 file), ggplot2 (1 file)
Availability: 1 check, the latest on 27 September 2026: the link answers
  • 27 September 2026: the link answers
30 files

gaospecial/ggVennDiagram

License: GPL-3.0
State: the link answers, verified on 27 September 2026
Evidence: files inventoried
Commit: 1312fac6076e7ac033d3188e2eb6153df3b35bdc, 10 January 2026
Languages: R (26)
Size: 83 files, 26 scripts
Software Heritage: not archived
Found in: the text, “Proteomic data analysis”
Holds: README, license file, environment (DESCRIPTION), tests, continuous integration, documentation, 6 notebooks
Not found: CITATION.cff
Tools: ggplot2 (9 files), tidyverse (8 files), cowplot (1 file), Plotly (1 file)
Availability: 1 check, the latest on 27 September 2026: the link answers
  • 27 September 2026: the link answers
28 files

mbojan/alluvial

License: other
State: the link answers, verified on 27 September 2026
Evidence: files inventoried
Commit: 4003444cb43c3b2bf8961951912563cd73c81629, 5 May 2026
Languages: R (11)
Size: 45 files, 11 scripts
Software Heritage: archived
Found in: the text, “Proteomic data analysis”
Holds: README, license file, environment (DESCRIPTION), tests, continuous integration, documentation, 2 notebooks
Not found: CITATION.cff
Tools: tidyverse (4 files), ggplot2 (1 file), reshape2 (1 file)
Availability: 1 check, the latest on 27 September 2026: the link answers
  • 27 September 2026: the link answers
13 files

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:

  • 3 repositories of the authors' code, each at its verified commit, with its license and how the link was found in the paper;
  • 65 scripts, each with its path and the digest of its content;
  • 13 matches 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

No dataset and no data link were found in the paper.

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 2, 28 September 2026

  • Publisher: n/a → The Company of Biologists

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 5 authors, 6 keywords, 9 MeSH terms, 6 funders, 105 references.

Cite

This paper

Krause, M., Kronberg, K. A., Girão, P. J. B., Strohmeier, L. S., & Quattrocolo, G. (2026). Proteomic profile of hippocampal growth cones through early postnatal development. Development (Cambridge, England), 153(12), dev205342. https://doi.org/10.1242/dev.205342

BibTeX

@article{krause2026proteomic,
author = {Krause, Maike and Kronberg, Kamilla Aase and Girão, Paulo J B and Strohmeier, Lara Sophie and Quattrocolo, Giulia},
title = {{Proteomic profile of hippocampal growth cones through early postnatal development}},
journal = {Development (Cambridge, England)},
year = {2026},
month = jun,
volume = {153},
number = {12},
pages = {dev205342},
publisher = {Company of Biologists},
issn = {0950-1991},
doi = {10.1242/dev.205342},
url = {https://doi.org/10.1242/dev.205342},
pmid = {42252990},
pmcid = {PMC13354955}
}

RIS

TY - JOUR
AU - Krause, Maike
AU - Kronberg, Kamilla Aase
AU - Girão, Paulo J B
AU - Strohmeier, Lara Sophie
AU - Quattrocolo, Giulia
TI - Proteomic profile of hippocampal growth cones through early postnatal development
T2 - Development (Cambridge, England)
J2 - Development
PY - 2026
DA - 2026/06/22
VL - 153
IS - 12
SP - dev205342
SN - 0950-1991
PB - Company of Biologists
DO - 10.1242/dev.205342
UR - https://doi.org/10.1242/dev.205342
LA - en
ER -

CSL-JSON

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"page": "dev205342",
"DOI": "10.1242/dev.205342",
"PMID": "42252990",
"PMCID": "PMC13354955",
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"date-parts": [
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Journal: iScience
In common: circlize, ComplexHeatmap, Plotly, 4 other tools, genetics / omics, 2 references
[10] doi:10.1002/cne.70106
Differences in Cajal-Retzius Cell Density and Postnatal Persistence Across Cortical Areas Revealed by a Novel Intersectional Genetic Labeling Approach.
Journal: The Journal of comparative neurology
In common: developmental, mouse, 3 references, author Giulia Quattrocolo

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