Literature DB >> 34191027

The subcortical maternal complex: emerging roles and novel perspectives.

Daniela Bebbere1, David F Albertini2, Giovanni Coticchio3, Andrea Borini3, Sergio Ledda1.   

Abstract

Since its recent discovery, the subcortical maternal complex (SCMC) is emerging as a maternally inherited and crucial biological structure for the initial stages of embryogenesis in mammals. Uniquely expressed in oocytes and preimplantation embryos, where it localizes to the cell subcortex, this multiprotein complex is essential for early embryo development in the mouse and is functionally conserved across mammalian species, including humans. The complex has been linked to key processes leading the transition from oocyte to embryo, including meiotic spindle formation and positioning, regulation of translation, organelle redistribution, and epigenetic reprogramming. Yet, the underlying molecular mechanisms for these diverse functions are just beginning to be understood, hindered by unresolved interplay of SCMC components and variations in early lethal phenotypes. Here we review recent advances confirming involvement of the SCMC in human infertility, revealing an unexpected relationship with offspring health. Moreover, SCMC organization is being further revealed in terms of novel components and interactions with additional cell constituents. Collectively, this evidence prompts new avenues of investigation into possible roles during the process of oogenesis and the regulation of maternal transcript turnover during the oocyte to embryo transition.
© The Author(s) 2021. Published by Oxford University Press on behalf of European Society of Human Reproduction and Embryology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  cytoplasmic lattices; early embryogenesis; genetic infertility; maternal effect mutations; maternal transcript degradation; multi-locus imprinting disturbance; oocyte subcortex; reproductive disorders

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Year:  2021        PMID: 34191027     DOI: 10.1093/molehr/gaab043

Source DB:  PubMed          Journal:  Mol Hum Reprod        ISSN: 1360-9947            Impact factor:   4.025


  3 in total

1.  Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances.

Authors:  Laura Pignata; Francesco Cecere; Ankit Verma; Bruno Hay Mele; Maria Monticelli; Basilia Acurzio; Carlo Giaccari; Angela Sparago; Jose Ramon Hernandez Mora; Ana Monteagudo-Sánchez; Manel Esteller; Arrate Pereda; Jair Tenorio-Castano; Orazio Palumbo; Massimo Carella; Paolo Prontera; Carmelo Piscopo; Maria Accadia; Pablo Lapunzina; Maria Vittoria Cubellis; Guiomar Perez de Nanclares; David Monk; Andrea Riccio; Flavia Cerrato
Journal:  Clin Epigenetics       Date:  2022-05-28       Impact factor: 7.259

2.  Germline variants in genes of the subcortical maternal complex and Multilocus Imprinting Disturbance are associated with miscarriage/infertility or Beckwith-Wiedemann progeny.

Authors:  Pierpaola Tannorella; Luciano Calzari; Cecilia Daolio; Ester Mainini; Alessandro Vimercati; Davide Gentilini; Fiorenza Soli; Annalisa Pedrolli; Maria Teresa Bonati; Lidia Larizza; Silvia Russo
Journal:  Clin Epigenetics       Date:  2022-03-22       Impact factor: 6.551

Review 3.  Oocyte aging: looking beyond chromosome segregation errors.

Authors:  Daniela Bebbere; Giovanni Coticchio; Andrea Borini; Sergio Ledda
Journal:  J Assist Reprod Genet       Date:  2022-02-25       Impact factor: 3.357

  3 in total

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