Unusual nuclear structures in male meiocytes of wild-type rye as revealed by volume microscopy

Author:

Mursalimov Sergey12,Matsumoto Mami34,Urakubo Hidetoshi35,Deineko Elena1,Ohno Nobuhiko67

Affiliation:

1. Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences , Novosibirsk, 630090 , Russia

2. Institute of Postharvest and Food Sciences, Agricultural Research Organization (ARO)-Volcani Institute , Rishon LeZion, 7505101 , Israel

3. Section of Electron Microscopy, Supportive Center for Brain Research, National Institute for Physiological Sciences , Okazaki, 444-8585 , Japan

4. Department of Developmental and Regenerative Neurobiology, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences , Nagoya, 467-8601 , Japan

5. Department of Biomedical Data Science, School of Medicine, Fujita Health University , Toyoake, 470-1192 , Japan

6. Department of Anatomy, Division of Histology and Cell Biology, School of Medicine, Jichi Medical University , Shimotsuke, 329-0431 , Japan

7. Division of Ultrastructural Research, National Institute for Physiological Sciences , Okazaki, 444-8585 , Japan

Abstract

Abstract Background and Aims During the analysis of plant male meiocytes coming from destroyed meiocyte columns (united multicellular structures formed by male meiocytes in each anther locule), a considerable amount of information becomes unavailable. Therefore, in this study intact meiocyte columns were studied by volume microscopy in wild-type rye for the most relevant presentation of 3-D structure of rye meiocytes throughout meiosis. Methods We used two types of volume light microscopy: confocal laser scanning microscopy and non-confocal bright-field scanning microscopy combined with alcohol and aldehyde fixation, as well as serial block-face scanning electron microscopy. Key Results Unusual structures, called nuclear protuberances, were detected. At certain meiotic stages, nuclei formed protuberances that crossed the cell wall through intercellular channels and extended into the cytoplasm of neighbouring cells, while all other aspects of cell structure appeared to be normal. This phenomenon of intercellular nuclear migration (INM) was detected in most meiocytes at leptotene/zygotene. No cases of micronucleus formation or appearance of binucleated meiocytes were noticed. There were instances of direct contact between two nuclei during INM. No influence of fixation or of mechanical impact on the induction of INM was detected. Conclusions Intercellular nuclear migration in rye may be a programmed process (a normal part of rye male meiosis) or a tricky artefact that cannot be avoided in any way no matter which approach to meiocyte imaging is used. In both cases, INM seems to be an obligatory phenomenon that has previously been hidden by limitations of common microscopic techniques and by 2-D perception of plant male meiocytes. Intercellular nuclear migration cannot be ignored in any studies involving manipulations of rye anthers.

Funder

National Institute for Physiological Sciences

Publisher

Oxford University Press (OUP)

Subject

Plant Science

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