PXD035225 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Cohesin is involved in transcriptional repression of invasion-related genes |
Description | The most virulent human malaria parasite, Plasmodium falciparum, has a complex life cycle between its human host and mosquito vector. Each stage is driven by a specific transcriptional program, but with a relatively high ratio of genes to specific transcription factors, it is unclear how genes are activated or silenced at specific times. The P. falciparum genome is relatively euchromatic compared to the mammalian genome, except for specific genes that are uniquely heterochromatinized via HP1. There seems to be an association between gene activity and spatial organization; however, the molecular mechanisms behind genome organization are unclear. While P. falciparum lacks lamins and CTCF – key metazoan genome-organizing proteins – it does have all core components of the cohesin complex. In other eukaryotes, cohesin is involved in sister chromatid cohesion, transcription, and genome organization. To investigate the role of cohesin in P. falciparum, we combined genome editing, mass-spectrometry, chromatin immunoprecipitation and sequencing (ChIP-seq), and RNA sequencing to functionally characterize the cohesin subunit Structural Maintenance of Chromosomes protein 3 (SMC3). SMC3 knockdown in early stages of the intraerythrocytic developmental cycle (IDC) resulted in significant up-regulation of a subset of genes involved in erythrocyte egress and invasion, which are normally expressed at later stages. ChIP-seq of SMC3 revealed that over the IDC, enrichment at the promoter regions of these genes inversely correlates with their expression. These data suggest that SMC3 binding helps to repress specific genes until their appropriate time of expression, revealing a new mode of gene repression in P. falciparum. |
HostingRepository | PRIDE |
AnnounceDate | 2023-11-14 |
AnnouncementXML | Submission_2023-11-14_09:05:41.976.xml |
DigitalObjectIdentifier | https://dx.doi.org/10.6019/PXD035225 |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Supported dataset by repository |
PrimarySubmitter | AMEYA SINHA |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | iodoacetamide derivatized residue |
Instrument | Q Exactive HF |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2022-07-11 08:03:17 | ID requested | |
1 | 2023-10-04 02:02:38 | announced | |
⏵ 2 | 2023-11-14 09:05:48 | announced | 2023-11-14: Updated project metadata. |
Publication List
10.6019/PXD035225; |
Rosa C, Singh P, Chen P, Sinha A, Cla, ë, s A, Preiser PR, Dedon PC, Baumgarten S, Scherf A, Bryant JM, Cohesin contributes to transcriptional repression of stage-specific genes in the human malaria parasite. EMBO Rep, 24(10):e57090(2023) [pubmed] |
Keyword List
submitter keyword: Plasmodium, SMC3, Cohesin |
Contact List
Peter R. Preiser |
contact affiliation | Vice President of Research, Nanyang Technological University |
contact email | prpreiser@ntu.edu.sg |
lab head | |
AMEYA SINHA |
contact affiliation | NTU |
contact email | ameya.sinha@gmail.com |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD035225
- Label: PRIDE project
- Name: Cohesin is involved in transcriptional repression of invasion-related genes