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Dual mechanism of chromatin remodeling in the common shrew sex trivalent (XY 1 Y 2 )
Here we focus on the XY Y condition in male common shrew Linnaeus, 1758, applying electron microscopy and immunocytochemistry for a comprehensive analysis of structure, synapsis and behaviour of the sex trivalent in pachytene spermatocytes. The pachytene sex trivalent consists of three distinct part...
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Published in: | Comparative cytogenetics 2017, Vol.11 (4), p.727-745 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Here we focus on the XY
Y
condition in male common shrew
Linnaeus, 1758, applying electron microscopy and immunocytochemistry for a comprehensive analysis of structure, synapsis and behaviour of the sex trivalent in pachytene spermatocytes. The pachytene sex trivalent consists of three distinct parts: short and long synaptic SC fragments (between the X and Y
and between the X and Y
, respectively) and a long asynaptic region of the X in-between. Chromatin inactivation was revealed in the XY
synaptic region, the asynaptic region of the X and a very small asynaptic part of the Y
. This inactive part of the sex trivalent, that we named the 'head', forms a typical sex body and is located at the periphery of the meiotic nucleus at mid pachytene. The second part or 'tail', a long region of synapsis between the X and Y
chromosomes, is directed from the periphery into the nucleus. Based on the distribution patterns of four proteins involved in chromatin inactivation, we propose a model of meiotic silencing in shrew sex chromosomes. Thus, we conclude that pachytene sex chromosomes are structurally and functionally two different chromatin domains with specific nuclear topology: the peripheral inactivated 'true' sex chromosome regions (part of the X and the Y
) and more centrally located transcriptionally active autosomal segments (part of the X and the Y
). |
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ISSN: | 1993-0771 1993-078X |
DOI: | 10.3897/CompCytogen.v11i4.13870 |