Literature DB >> 31575650

The subcortical maternal complex protein Nlrp4f is involved in cytoplasmic lattice formation and organelle distribution.

Dandan Qin1,2, Zheng Gao1,3, Yi Xiao1, Xiaoxin Zhang1, Haixia Ma1, Xingjiang Yu1, Xiaoqing Nie1,2, Na Fan4, Xiaoqing Wang1, Yingchun Ouyang1, Qing-Yuan Sun1, Zhaohong Yi4, Lei Li5,2.   

Abstract

In mammalian oocytes and embryos, the subcortical maternal complex (SCMC) and cytoplasmic lattices (CPLs) are two closely related structures. Their detailed compositions and functions remain largely unclear. Here, we characterize Nlrp4f as a novel component associated with the SCMC and CPLs. Disruption of maternal Nlrp4f leads to decreased fecundity and delayed preimplantation development in the mouse. Lack of Nlrp4f affects organelle distribution in mouse oocytes and early embryos. Depletion of Nlrp4f disrupts CPL formation but does not affect the interactions of other SCMC proteins. Interestingly, the loss of Khdc3 or Tle6, two other SCMC proteins, also disrupts CPL formation in mouse oocytes. Thus, the absence of CPLs and aberrant distribution of organelles in the oocytes caused by disruption of the examined SCMC genes, including previously reported Zbed3, Nlrp5, Ooep and Padi6, indicate that the SCMC is required for CPL formation and organelle distribution. Consistent with the role of the SCMC in CPL formation, the SCMC forms before CPLs during mouse oogenesis. Together, our results suggest that the SCMC protein Nlrp4f is involved in CPL formation and organelle distribution in mouse oocytes.
© 2019. Published by The Company of Biologists Ltd.

Entities:  

Keywords:  Cytoplasmic lattices; Maternal effect gene; NLRP; Oocyte-to-embryo transition; Organelle; SCMC

Year:  2019        PMID: 31575650     DOI: 10.1242/dev.183616

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  6 in total

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Review 2.  Molecular tools for the genomic assessment of oocyte's reproductive competence.

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3.  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

4.  Maternally contributed Nlrp9b expressed in human and mouse ovarian follicles contributes to early murine preimplantation development.

Authors:  Mahboobeh Amoushahi; Line Lawaetz Steffensen; Adelya Galieva; Jens Agger; Anders Heuck; Piotr Siupka; Erik Ernst; Morten S Nielsen; Lone Sunde; Karin Lykke-Hartmann
Journal:  J Assist Reprod Genet       Date:  2020-05-12       Impact factor: 3.412

5.  Two novel mutations in PADI6 and TLE6 genes cause female infertility due to arrest in embryonic development.

Authors:  Juan Liu; Zongjian Tan; Jun He; Tingting Jin; Yuanyuan Han; Li Hu; Shengwen Huang
Journal:  J Assist Reprod Genet       Date:  2021-05-26       Impact factor: 3.412

6.  CRISPR/Cas9-Mediated Genome Editing Reveals Oosp Family Genes are Dispensable for Female Fertility in Mice.

Authors:  Ferheen Abbasi; Mayo Kodani; Chihiro Emori; Daiji Kiyozumi; Masashi Mori; Yoshitaka Fujihara; Masahito Ikawa
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  6 in total

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