Literature DB >> 16048630

The chromatoid body in spermatogenesis.

Martti Parvinen1.   

Abstract

All germ cells throughout the animal kingdom contain cytoplasmic cloud-like accumulations of material called nuage. Polar bodies in Drosophila oocytes are probably the best known forms of nuage. In spermatogenic cells, the nuage is called chromatoid body (CB). In early spermatids of the rat, it has a diameter of 1-1.5 microm and a finely filamentous lobular structure. Typically, it is associated with a multitude of vesicles. It is first clearly seen in mid- and late pachytene spermatocytes as an intermitochondrial dense material. During early spermiogenesis it is seen near the Golgi complex and frequently connected by material continuities through nuclear pore complexes with intranuclear particles. In living cells, the CB moves around the Golgi complex and has frequent contacts with it. The CB also moves perpendicularly to the nuclear envelope, and even through cytoplasmic bridges to the neighbour spermatids. One of the major components of the CB is a DEAD-box RNA helicase VASA that belongs to a class of proteins thought to act as RNA chaperones. It is a general marker of all germ cells and best characterized in Drosophila. The mouse VASA homologue was recently used as a marker of sperm formation from embryonic stem cells. It becomes generally accepted that the CB with its associated structures constitute a mechanism of post-transcriptional processing and storage of several mRNA species that are shared between neighbour cells and used for translation when the genome of the spermatids becomes inactive.

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Year:  2005        PMID: 16048630     DOI: 10.1111/j.1365-2605.2005.00542.x

Source DB:  PubMed          Journal:  Int J Androl        ISSN: 0105-6263


  45 in total

1.  Identification of SAMT family proteins as substrates of MARCH11 in mouse spermatids.

Authors:  Keiichiro Yogo; Hidehiro Tojima; Jun-Ya Ohno; Takuya Ogawa; Nobuhiro Nakamura; Shigehisa Hirose; Tatsuo Takeya; Tetsuya Kohsaka
Journal:  Histochem Cell Biol       Date:  2011-11-11       Impact factor: 4.304

Review 2.  New insights into the regulation of RNP granule assembly in oocytes.

Authors:  Jennifer A Schisa
Journal:  Int Rev Cell Mol Biol       Date:  2012       Impact factor: 6.813

3.  Genetic variation of copia suppression in Drosophila melanogaster.

Authors:  W Vu; S Nuzhdin
Journal:  Heredity (Edinb)       Date:  2010-07-07       Impact factor: 3.821

4.  Vasa genes: emerging roles in the germ line and in multipotent cells.

Authors:  Eric A Gustafson; Gary M Wessel
Journal:  Bioessays       Date:  2010-07       Impact factor: 4.345

5.  MIWI associates with translational machinery and PIWI-interacting RNAs (piRNAs) in regulating spermatogenesis.

Authors:  Shane T Grivna; Brook Pyhtila; Haifan Lin
Journal:  Proc Natl Acad Sci U S A       Date:  2006-08-24       Impact factor: 11.205

Review 6.  Small RNAs and RNAi pathways in meiotic prophase I.

Authors:  Rebecca J Holmes; Paula E Cohen
Journal:  Chromosome Res       Date:  2007       Impact factor: 5.239

Review 7.  Nuage proteins: their localization in subcellular structures of spermatogenic cells as revealed by immunoelectron microscopy.

Authors:  Sadaki Yokota
Journal:  Histochem Cell Biol       Date:  2012-05-15       Impact factor: 4.304

8.  Aging and chromatoid body assembly: Are these two physiological events linked?

Authors:  Elisa G Santos; Maraisa A Silva; Renata P Amorim; Leticia de Souza Giordano; Dayana de Sales Silva; Lucas T Rasmussen; Rita L Peruquetti
Journal:  Exp Biol Med (Maywood)       Date:  2018-06-29

Review 9.  RNA granules in germ cells.

Authors:  Ekaterina Voronina; Geraldine Seydoux; Paolo Sassone-Corsi; Ippei Nagamori
Journal:  Cold Spring Harb Perspect Biol       Date:  2011-12-01       Impact factor: 10.005

Review 10.  Post-transcriptional regulation in budding yeast meiosis.

Authors:  Liang Jin; Aaron M Neiman
Journal:  Curr Genet       Date:  2015-11-27       Impact factor: 3.886

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