Role of DNA methylation reprogramming in germline stress response

Projektinformationen

MASTER

ID Finanzhilfevereinbarung: 101033109

DOI

10.3030/101033109

Projekt abgeschlossen

EK-Unterschriftsdatum 4 März 2021

Startdatum 1 April 2021

Enddatum 31 März 2023

Finanziert unter

• EXCELLENT SCIENCE - Marie Skłodowska-Curie Actions

Gesamtkosten

€ 224 933,76

EU-Beitrag

€ 224 933,76

Koordiniert durch

JOHN INNES CENTRE
United Kingdom

Periodic Reporting for period 1 - MASTER (Role of DNA methylation reprogramming in germline stress response)

Berichtszeitraum: 2021-04-01 bis 2023-03-31

Zusammenfassung vom Kontext und den Gesamtzielen des Projekts

Although the male germline DNA methylomes and their dynamics have been well studied, how the methylation pattern was established in germ cells was elusive. Our discoveries elucidate essential methylation and regulatory mechanisms in plant germlines that mediate intergenerational heredity, and establish a novel epigenetic paradigm in how germlines perceive and respond to stress.

Our discoveries reveal a new mechanism suggesting how DNA methylation was established in male germ cells directed by its nurse cells. Above all, our works indicate how this pathway mentioned above is involved in the ambient temperature sense, uncovering a novel molecular regulation mechanism in plant germline thermotolerance, which is believed to impact the relative research field.

The overall objectives have been successfully achieved including 1) Elucidate DNA methylation reprogramming in the Arabidopsis germline, 2) Determine the role of methylation reprogramming in mediating male thermotolerance, 3) Uncover the biological functions of methylation reprogramming in the germline.

Arbeit, die ab Beginn des Projekts bis zum Ende des durch den Bericht erfassten Berichtszeitraums geleistet wurde, und die wichtigsten bis dahin erzielten Ergebnisse

We developed a method to isolate Arabidopsis tapetal cells and draw DNA methylation status and siRNA landscapes in meiocyte and tapetum. Our result indicates the siRNA was generated in tapetal cells and transferred to meiocyte to assist DNA methylation establishment. Additionally, we found HSP70T which is a GSMs (Germline Spefic Methylation), was regulated by tapetal origin siRNA and its methylation and transcription were sensitive and regulated by ambient temperature. Moreover, we found this kind of response pathway was mediated by RdDM. Collectively, we identified a novel thermotolerance mechanism in plant germ cells.

Fortschritte, die über den aktuellen Stand der Technik hinausgehen und voraussichtliche potenzielle Auswirkungen (einschließlich der bis dato erzielten sozioökonomischen Auswirkungen und weiter gefassten gesellschaftlichen Auswirkungen des Projekts)

Our project has been completed, all the main results are represented in the final report. Our work uncovers a novel mechanism for how DNA methylation was established via siRNA transportation from tapetum, and reveals its linkage with gametophyte thermotolerance. It would be the first reported work clarifying the mechanism of how siRNA senses ambient temperature and react to high-temperature tolerance. These would be believed to impact the relative academic field.

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