Literature DB >> 7958403

The centrosome and its mode of inheritance: the reduction of the centrosome during gametogenesis and its restoration during fertilization.

G Schatten1.   

Abstract

Neither the restoration of the centrosome during fertilization nor its reduction during gametogenesis is fully understood, but both are pivotal events in development. During each somatic cell cycle, the chromosomes, cytoplasm, and centrosomes duplicate in interphase, and all three split in two during each cell division. While it has long been recognized that both the sperm and the egg contribute equal haploid genomes during fertilization and that the vast majority of the cytoplasm is contributed by the egg, the relative contributions of the centrosome by each gamete are still in question. This article explores centrosome inheritance patterns and considers nine integral and secondarily derived activities of the centrosome. Boveri once hypothesized that "The ripe egg possesses all of the elements necessary for development save an active division-center. The sperm, on the other hand, possesses such a center but lacks the protoplasmic substratum in which to operate. In this respect the egg and sperm are complementary structures; their union in syngamy thus restores to each the missing element necessary to further development." This article reviews the evidence gathered from 11 experimental strategies used to test this theory. While the majority of these approaches supports the hypothesis that the sperm introduces the centrosome at fertilization, the pattern did not reveal itself as universal, since parthenogenesis occurs in nature and can be induced artificially, since centrosome and centriole form de novo in extracts from unfertilized eggs and since the centrosome is derived from maternal sources during fertilization in some systems--notably, in mice. Models of the centrosome are proposed, along with speculative mechanisms which might lead to the cloaking of the reproducing element of the maternal centrosome during oogenesis and the retention of this structure by the paternal centrosome during spermatogenesis. Proteins essential for microtubule nucleation, like gamma-tubulin, are retained in the cytoplasm during oogenesis, but are largely lost during spermatogenesis. It is further postulated that the restoration of the zygotic centrosome at fertilization requires the attraction of maternal centrosomal components (in particular, gamma-tubulin and the 25S "gamma-some" particle) to the paternal reproducing element; this, along with post-translational modifications (including phosphorylation, disulfide reduction, and calcium ion binding), creates a functional zygote centrosome by blending both maternal and paternal constituents.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1994        PMID: 7958403     DOI: 10.1006/dbio.1994.1256

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  113 in total

1.  Centrosome amplification and chromosomal instability in human and animal parthenogenetic cell lines.

Authors:  Tiziana A L Brevini; Georgia Pennarossa; Sara Maffei; Gianluca Tettamanti; Arianna Vanelli; Sara Isaac; Amir Eden; Sergio Ledda; Magda de Eguileor; Fulvio Gandolfi
Journal:  Stem Cell Rev Rep       Date:  2012-12       Impact factor: 5.739

2.  Pronuclear and morphological features as a cumulative score to select embryos in ICSI (intracytoplasmic sperm injection) cycles according to sperm origin.

Authors:  Lia Mara Rossi-Ferragut; Assumpto Iaconelli; Tsutomu Aoki; Claudia Chagas Rocha; Daniela Regina dos Santos; Fábio Firmbach Pasqualotto; Edson Borges
Journal:  J Assist Reprod Genet       Date:  2003-01       Impact factor: 3.412

3.  Analysis of centriole elimination during C. elegans oogenesis.

Authors:  Tamara Mikeladze-Dvali; Lukas von Tobel; Petr Strnad; Graham Knott; Heinrich Leonhardt; Lothar Schermelleh; Pierre Gönczy
Journal:  Development       Date:  2012-05       Impact factor: 6.868

4.  Different sperm sources and parameters can influence intracytoplasmic sperm injection outcomes before embryo implantation.

Authors:  Yue-hong Lu; Hui-juan Gao; Bai-jia Li; Ying-ming Zheng; Ying-hui Ye; Yu-li Qian; Chen-ming Xu; He-feng Huang; Fan Jin
Journal:  J Zhejiang Univ Sci B       Date:  2012-01       Impact factor: 3.066

Review 5.  The Janus soul of centrosomes: a paradoxical role in disease?

Authors:  Maddalena Nano; Renata Basto
Journal:  Chromosome Res       Date:  2016-01       Impact factor: 5.239

Review 6.  Differentiating the roles of microtubule-associated proteins at meiotic kinetochores during chromosome segregation.

Authors:  Yasutaka Kakui; Masamitsu Sato
Journal:  Chromosoma       Date:  2015-09-17       Impact factor: 4.316

7.  Differential regulation of maternal vs. paternal centrosomes.

Authors:  X Wu; R E Palazzo
Journal:  Proc Natl Acad Sci U S A       Date:  1999-02-16       Impact factor: 11.205

8.  Genetic and molecular characterization of the caenorhabditis elegans gene, mel-26, a postmeiotic negative regulator of mei-1, a meiotic-specific spindle component.

Authors:  M R Dow; P E Mains
Journal:  Genetics       Date:  1998-09       Impact factor: 4.562

9.  A proximal centriole-like structure is present in Drosophila spermatids and can serve as a model to study centriole duplication.

Authors:  Stephanie Blachon; Xuyu Cai; Kela A Roberts; Kevin Yang; Andrey Polyanovsky; Allen Church; Tomer Avidor-Reiss
Journal:  Genetics       Date:  2009-03-16       Impact factor: 4.562

Review 10.  Vertebrate maternal-effect genes: Insights into fertilization, early cleavage divisions, and germ cell determinant localization from studies in the zebrafish.

Authors:  Robin E Lindeman; Francisco Pelegri
Journal:  Mol Reprod Dev       Date:  2010-04       Impact factor: 2.609

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