| Literature DB >> 35090020 |
Christophe Tatout1, Guillaume Mougeot1,2, Geraint Parry3,4, Célia Baroux5, Mónica Pradillo6, David Evans2.
Abstract
This Community Resource paper introduces the range of materials developed by the INDEPTH (Impact of Nuclear Domains on Gene Expression and Plant Traits) COST Action made available through the INDEPTH Academy. Recent rapid growth in understanding of the significance of epigenetic controls in plant and crop science has led to a need for shared, high-quality resources, standardization of protocols, and repositories for open access data. The INDEPTH Academy provides a range of masterclass tutorials, standardized protocols, and teaching webinars, together with a rapidly developing repository to support imaging and spatial analysis of the nucleus and deep learning for automated analysis. These resources were developed partly as a response to the COVID-19 pandemic, but also driven by needs and opportunities identified by the INDEPTH community of ~200 researchers in 80 laboratories from 32 countries. This community report outlines the resources produced and how they will be extended beyond the INDEPTH project, but also aims to encourage the wider community to engage with epigenetics and nuclear structure by accessing these resources.Entities:
Keywords: COST Action; image repository; plants; protocols; tutorials; webinars
Mesh:
Year: 2022 PMID: 35090020 PMCID: PMC8982392 DOI: 10.1093/jxb/erac005
Source DB: PubMed Journal: J Exp Bot ISSN: 0022-0957 Impact factor: 6.992
Fig. 1.Knowledge and resources generated by INDEPTH.
Standardized protocols to study the plant nucleus
| Protocol | Advising author(s) | Work Group | DOI |
|---|---|---|---|
| Hi-C protocol for analysis of plant nuclear chromatin interactions | Chang Liu and Silin Zhong | WG4 |
|
| Single molecular fluorescence | Stefanie Rosa | WG2 |
|
| Localizing total mRNA in plant cells | Geraint Parry | WG2 |
|
| Fluorescence-activated nuclear sorting (FANS) | Ortrun Mittelsten Scheid | WG2 |
|
| Protocol for isolation of plant nucleolus | Frederic Pontvianne | WG2 |
|
| Assay for transposase-accessible chromatin (ATAC-seq) | Roger Deal and Kenneth Berendzen | WG4 |
|
| Membrane yeast two-hybrid (MYTH) | Christophe Tatout and Emmanuel Vanrobays | WG2 |
|
Teaching webinars on chromatin domains and chromatin dynamics in the plant nucleus
| Webinar Title | Author | Work Group | Weblink |
|---|---|---|---|
| Endoreduplication in tomato fruit growth | Christian Chevalier | WG3 |
|
| Linker histones | Célia Baroux | WG1 |
|
| Introduction to the plant nuclear pore complex | Geraint Parry | WG2 |
|
| The role of chromatin domains in plant meiosis | Mónica Pradillo | WG3 |
|
| Temperature and sexual reproduction | Danny Geelen | WG3 |
|
| Functions of plant nucleolus | Frederic Pontvianne | WG2 |
|
| The fascinating biology of plant pathogenic viroids | Kriton Kalantidis | WG3 |
|
Teaching webinars of selected short-term scientific missions (STSMs)
| STSM talk titles | Author | Work Group | Weblink |
|---|---|---|---|
| Understanding the impact of chromatin organization on transcriptional memory in plants | Emilia Cepowska | WG2 |
|
| Gene dosage composition of rDNA | Francesca Lopez | WG2 |
|
| Hi-C analysis of H1-mediated chromatin organization | Gianluca Teano | WG2 |
|
Masterclass tutorials on experimental techniques to study the plant nucleus
| Masterclass Tutorials Title | Presenting expert(s) | Work Group | Weblink |
|---|---|---|---|
| Spatial analysis of nuclear signal distribution using IMARISBitplane and DATAVIZUZH | Célia Baroux | WG1 |
|
| NucleusJ2.0 | Christophe Tatout and Sophie Desset | WG1 |
|
| INDEPTH OMERO 3D Image Repository | Hank Bass | WG1 |
|
| Fluorescence-activated nuclear sorting (FANS) | Ruben Gutzat | WG2 |
|
| Single molecular fluorescence | Stefanie Rosa | WG2 |
|
| Active segmentation as a tool for plant image analysis | Dimiter Prodanov | WG1 |
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| Plant functional proteomics | Vicente Rubio | WG2 |
|
| Size-exclusion chromatography coupled to multiangle light scattering (SEC-MALS)—a powerful tool for characterization of macromolecular complexes | Mariusz Czarnocki-Cieciura | WG4 |
|
List of 3D images included in the INDEPTH OMERO repository
| Projects | Names | Species and samples | Staining and image pre-treatment | Microscopy parameters | OMERO links | Number |
|---|---|---|---|---|---|---|
|
| IDP1001 |
| DAPI | Olympus 1-UB932 |
| 2 |
| IDP1002 |
| DAPI-EDU | Olympus 1-UB932 |
| 18 | |
| IDP1003 |
| DAPI | Olympus 1-UB932 |
| 7 | |
| IDP1004 |
| DAPI, DNA FISH FITC (telomeres), DNA FISH Rhodamine (chromosome9) | Olympus 1-UB932 |
| 5 | |
| IDP1005 |
| DAPI, Immunolocalization of ASY1, ZYP1, MLH1and RAD51 (FITC)-ASY1 (Cy3) | Olympus DP71 × 20 |
| 215 | |
|
| IDP2001 |
| DAPI | Leica MMAF+OptiGrid |
| 77 |
| IDP2002 |
| DAPI | Leica MMAF+OptiGrid |
| 28 | |
|
| IDP3001 |
| DAPI | Leica MMAF+OptiGrid |
| 77 |
| IDP3002 |
| DAPI, immunofluorescence, and DNA FISH | Multiple |
| 30 | |
| IDP3003 |
| DAPI-EDU | Olympus 1-UB932 |
| 287 | |
| IDP3004 |
| DNA staining (580CP dye) and DNA FISH 45S rDNA+180 bp satellite repeat | Leica SP8R WL 3×STED 0.02 × 0.02 × 0.13 |
| 2 | |
| IDP3005 |
| DAPI (cyan/blue), EdU (AF488, green) and DNA FISH 45S rDNA (AF594, red) | Zeiss Axioimager Z1 |
| 11 | |
| IDP3006 |
| DAPI DAPI -DNA FISH 5S rDNA ()- 180 bp satellite repeat | Leica MMAF+OptiGrid |
| 2477 | |
| IDP3007 |
| DNA staining= 580CP dye | Leica SP8R WL 3×STED 0.04 × 0.04 × 0.06 |
| 6 | |
|
| IDP4001 |
| DAPI | Leica MMAF+OptiGrid |
| 10 |
| IDP4002 |
| DAPI | Leica MMAF+OptiGrid |
| 413 |
Fig. 2.Image segmentation of a 3D nucleus from the IDP4002 dataset through the Mask-RCNN deep-learning model. Example of a raw image of a 3D nucleus from the IDP4002 dataset (left), the corresponding 3D segmentation performed semi-automatically with ilastik (middle), and the automatic segmentation obtained with Mask-RCNN pre-trained on a 2D dataset of nuclei (right). The small extra objects segmented in this last image illustrate the noise sensitivity of Mask-RCNN on our dataset and the need for retraining it.