| Literature DB >> 27165042 |
Frantzeskos Papanikos1, Katrin Daniel2, Angelique Goercharn-Ramlal3, Ji-Feng Fei4, Thomas Kurth4, Lukasz Wojtasz1, Ihsan Dereli1, Jun Fu2, Josef Penninger5, Bianca Habermann6, Azim Surani7, A Francis Stewart2, Attila Toth8.
Abstract
Meiosis is a critical phase in the life cycle of sexually reproducing organisms. Chromosome numbers are halved during meiosis, which requires meiosis-specific modification of chromosome behaviour. Furthermore, suppression of transposons is particularly important during meiosis to allow the transmission of undamaged genomic information between generations. Correspondingly, specialized genome defence mechanisms and nuclear structures characterize the germ line during meiosis. Survival of mammalian spermatocytes requires that the sex chromosomes form a distinct silenced chromatin domain, called the sex body. An enigmatic spherical DNA-negative structure, called the meiotic dense body, forms in association with the sex body. The dense body contains small non-coding RNAs including microRNAs and PIWI-associated RNAs. These observations gave rise to speculations that the dense body may be involved in sex body formation and or small non-coding RNA functions, e.g. the silencing of transposons. Nevertheless, the function of the dense body has remained mysterious because no protein essential for dense body formation has been reported yet. We discovered that the polycomb-related sex comb on midleg-like 1 (SCML1) is a meiosis-specific protein and is an essential component of the meiotic dense body. Despite abolished dense body formation, Scml1-deficient mice are fertile and proficient in sex body formation, transposon silencing and in timely progression through meiosis and gametogenesis. Thus, we conclude that dense body formation is not an essential component of the gametogenetic program in the mammalian germ line.Entities:
Keywords: Dense body; Meiosis; Polycomb; Transposon; piRNA
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Year: 2016 PMID: 27165042 PMCID: PMC7326603 DOI: 10.1007/s00412-016-0598-1
Source DB: PubMed Journal: Chromosoma ISSN: 0009-5915 Impact factor: 4.316