XY chromosomal bivalent: Nucleolar attraction

• Published in: Molecular reproduction and development 2005-09, Vol.72 (1), p.1-6
• Main Author: Tres, Laura L.
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Cell Nucleolus - genetics; Cell Nucleolus - physiology; Chromatin. Chromosome; Fundamental and applied biological sciences. Psychology; H2AX; Humans; Male; male meiotic prophase; Molecular and cellular biology; Molecular genetics; nucleolus; Pachytene Stage - genetics; Pachytene Stage - physiology; sex body; sex vesicle; synaptonemal complex; Synaptonemal Complex - genetics; Synaptonemal Complex - physiology; X Chromosome - genetics; X Chromosome - physiology; Xmr; XY bivalent; Y Chromosome - genetics; Y Chromosome - physiology
• ISSN: 1040-452X; 1098-2795
• DOI: 10.1002/mrd.20334

Nucleolar organization by autosomal bivalents occurs during male meiotic prophase in mammalian species. During late leptotene–early zygotene stages, several autosomal bivalents are engaged in ribosomal RNA synthesis. At pachytene stage, nucleolar masses detach from the sites of primary autosomal origin, relocate close to the XY chromosomal pair, and nucleolar components become segregated. In early pachytene, an extensive synaptonemal complex at the pseudoautosomal region, links X and Y chromosomes in close juxtaposition along most of the length of the Y chromosome, except for a terminal region of the Y that diverges from the pairing region. As meiotic prophase advances, X and Y chromosomes progressively desynapse and, at diplotene, the XY pair is associated end‐to‐end. Xmr (Xlr‐related, meiosis regulated) is a protein component of the nucleolus associated to the XY pair and of the asynapsed portions of the X and Y axial cores. Xmr, like SCP3, is a component of the lateral element of the synaptonemal complex. Both share structural homology in their C‐terminal region. This region contains several putative coiled‐coil domains known to mediate heterodimeric protein–protein interactions and to provide binding sites to regulatory proteins. Like Xmr, the tumor repressor protein BRCA1 is present along the unsynapsed cores of the XY bivalent. Both Xmr and BRCA1 have been implicated in a mechanism leading to chromatin condensation and transcription inactivation of the XY bivalent. The BRCA1‐ATR kinase complex, as recent research suggests, triggers the phosphorylation of histone H2AX, which predominates in the condensed chromatin of the XY chromosomal pair. Xmr is not present in the XY bivalent when the expression of histone H2AX is deficient. The role of Xmr in chromatin condensation of the XY bivalent has not been determined. The partial structural homology of SCP3 and Xmr, their distribution along the unsynapsed axial cores of the X and Y chromosomes, and the presence of Xmr in the XY pair‐associated nucleolus raises the possibility that Xmr, and other proteins including protein kinases, may be recruited to the nucleolus to perform functions related to chromosomal synapsis, chromatin condensation and recombination processes, as well as cell cycle progression. Mol. Reprod. Dev. © 2005 Wiley‐Liss, Inc.