Dataset Information

TMT-based phosphoproteomics and proteomics analysis of the developing mouse heart

ABSTRACT: We Investigate of the mice hearts from embryonic day 10.5 to postnatal week 8 and reveal developmental changes in phosphoproteome, proteome encompassing cardiogenesis and cardiac maturation.

INSTRUMENT(S): Orbitrap Fusion Lumos

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Heart

SUBMITTER: xiangzheng zhang

LAB HEAD: Xuejiang guo

PROVIDER: PXD036824 | Pride | 2023-01-17

REPOSITORIES: Pride

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Dataset's files

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			Action	DRS
	TMT10_MMHeart_Tissue_HPRP_Group1_F10_20200408.raw	Raw
	TMT10_MMHeart_Tissue_HPRP_Group1_F11_20200408.raw	Raw
	TMT10_MMHeart_Tissue_HPRP_Group1_F12_20200408.raw	Raw
	TMT10_MMHeart_Tissue_HPRP_Group1_F13_20200408.raw	Raw
	TMT10_MMHeart_Tissue_HPRP_Group1_F14_20200408.raw	Raw

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Publications

Multi-omics profiling visualizes dynamics of cardiac development and functions.

Gu Yayun Y Zhou Yan Y Ju Sihan S Liu Xiaofei X Zhang Zicheng Z Guo Jia J Gao Jimiao J Zang Jie J Sun Hao H Chen Qi Q Wang Jinghan J Xu Jiani J Xu Yiqun Y Chen Yingjia Y Guo Yueshuai Y Dai Juncheng J Ma Hongxia H Wang Cheng C Jin Guangfu G Li Chaojun C Xia Yankai Y Shen Hongbing H Yang Yang Y Guo Xuejiang X Hu Zhibin Z

Cell reports 20221201 13

Cardiogenesis is a tightly regulated dynamic process through a continuum of differentiation and proliferation events. Key factors and pathways governing this process remain incompletely understood. Here, we investigate mice hearts from embryonic day 10.5 to postnatal week 8 and dissect developmental changes in phosphoproteome-, proteome-, metabolome-, and transcriptome-encompassing cardiogenesis and cardiac maturation. We identify mitogen-activated protein kinases as core kinases involved in tra ...[more]

PMID: 36577384

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Project description:We previously demonstrated that inactivation of the replication checkpoint via a mec1 mutation led to chromosome breakage at replication forks initiated from virtually all origins of replication, after transient exposure to hydroxyurea (HU), an inhibitor of ribonucleotide reductase. Furthermore, we have shown that chromosomes break at replication forks that have suffered single-stranded DNA (ssDNA) formation. Here we sought to determine whether all replication forks containing ssDNA gaps have equal probability of producing double strand breaks (DSBs) when cells attempt to recover from HU exposure. We devised a new methodology, Break-Seq, that combines our previously described DSB labeling with NextGen sequencing to map chromosome breaks with improved sensitivity and resolution. We show that DSBs preferentially occur at genes transcriptionally induced by HU. Notably, different subsets of the HU-induced genes produced DSBs in MEC1 and mec1 cells as replication forks traversed greater distance in MEC1 cells than in mec1 cells during the recovery from HU. Specifically, while MEC1 cells exhibited chromosome breakage at stress-response transcription factors, mec1 cells predominantly suffered chromosome breakage at transporter genes, many of which are the substrates of the said transcription factors. We propose that HU-induced chromosome fragility arises at higher frequency near HU-induced genes as a result of destabilized replication forks encountering transcription factor binding and/or the act of transcription. Our model provides an explanation for a long-standing problem in chromosome biology: why different replication inhibitors produce different spectra of chromosome breakage? We propose that different inhibitors elicit different transcription responses as well as destabilize replication forks, and, when the two processes collide, ssDNA at the replication fork suffers further strand breakage, causing DSBs. We queried the yeast genome for DSBs after cells were treated with 200 mM hydroxyurea during S phase. Samples were collected from 1) cells synchronized in G1 phase by alpha factor; 2) cells released from G1 into medium containing 200 mM hydroxyurea for 1 h; 3) cells recovering in fresh medium without hydroxyurea for 1 h after the 1 h exposure to HU. These samples are referred to as G1, HU 1h, and R 1h, respectively. The strains from which the samples were collected are indicated following the time point, e.g. G1_MEC1 or R 1h_mec1. The experiment with mec1 was done twice (Experiments A and B) and that with MEC1 was done once (Experiment C). In addition, a control experiment of in vitro digestion with BamHI using the G1_mec1 sample (G1_BamHI) was performed.