During meiotic arrest, and particularly during the oocyte growth phase leading to the formation of fully-grown oocyte, the chromatin enclosed within the oocyte nucleus, also known as Germinal Vesicle (GV), is subjected to several levels of regulation controlling both its structure and function. These events include mechanisms acting both locally, on specific loci, and on a large scale to remodel wide portions of the oocyte genome. Morphologically, the chromosomes lose their individuality as well as their characteristic appearance and form a loose chromatin mass, which in turn undergoes profound and dynamic rearrangements within the GV before the meiotic resumption. These ‘large-scale chromatin configuration changes’ are temporally correlated with the process of transcriptional silencing in the oocyte nucleus as well as with epigenetic modifications such as histone tail modifications and changes in the global level of DNA methylation. Moreover, chromatin configuration rearrangements are tightly associated with the acquisition of meiotic and developmental competence. The molecular mechanisms governing changes in large-scale chromatin configuration still remain largely unknown. Most likely, strategies set in place for the control and coordination of these events are part of a complex physiological process that ultimately confers the oocyte with meiotic and developmental competence. Here, we summarize some studies intended to explain the mechanism(s) regulating this complex process.

Dynamics and regulatory mechanisms involved in immature oocyte chromatin remodeling / V. Lodde, S.C. Modina, M.E. Andreis, L. Terzaghi, A.M. Luciano. - In: MICROSCOPIE. - 13:2(2016), pp. 42-42. ((Intervento presentato al convegno Nuclear structure and dynamics, through the microscopes tenutosi a Pavia nel 2016.

Dynamics and regulatory mechanisms involved in immature oocyte chromatin remodeling

V. Lodde
Primo
;
S.C. Modina
Secondo
;
M.E. Andreis;L. Terzaghi
Penultimo
;
A.M. Luciano
Ultimo
2016

Abstract

During meiotic arrest, and particularly during the oocyte growth phase leading to the formation of fully-grown oocyte, the chromatin enclosed within the oocyte nucleus, also known as Germinal Vesicle (GV), is subjected to several levels of regulation controlling both its structure and function. These events include mechanisms acting both locally, on specific loci, and on a large scale to remodel wide portions of the oocyte genome. Morphologically, the chromosomes lose their individuality as well as their characteristic appearance and form a loose chromatin mass, which in turn undergoes profound and dynamic rearrangements within the GV before the meiotic resumption. These ‘large-scale chromatin configuration changes’ are temporally correlated with the process of transcriptional silencing in the oocyte nucleus as well as with epigenetic modifications such as histone tail modifications and changes in the global level of DNA methylation. Moreover, chromatin configuration rearrangements are tightly associated with the acquisition of meiotic and developmental competence. The molecular mechanisms governing changes in large-scale chromatin configuration still remain largely unknown. Most likely, strategies set in place for the control and coordination of these events are part of a complex physiological process that ultimately confers the oocyte with meiotic and developmental competence. Here, we summarize some studies intended to explain the mechanism(s) regulating this complex process.
Settore VET/01 - Anatomia degli Animali Domestici
2016
Article (author)
File in questo prodotto:
File Dimensione Formato  
Lodde_NuclearStructureDynamics_pg42_2016.pdf

accesso riservato

Tipologia: Publisher's version/PDF
Dimensione 59.74 kB
Formato Adobe PDF
59.74 kB Adobe PDF   Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/501294
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact