A stepwise route to domesticate rice by controlling seed shattering and panicle shape

Ryo Ishikawa, Cristina Cobo Castillo, Than Myint Htun, Koji Numaguchi, Kazuya Inoue, Yumi Oka, Miki Ogasawara, Shohei Sugiyama, Natsumi Takama, Chhourn Orn, Chizuru Inoue, Ken-Ichi Nonomura, Robin Allaby, Dorian Q Fuller and Takashige Ishii

PNAS (2022) 119, e2121692119 DOI:10.1073/pnas.2121692119

Press release (In Japanese only)

The international collaborative group of Kobe University, National Institute of Genetics (NIG), University of Warwick, University College London, Yezin Agricultural University, Cambodian Agricultural Research and Development Institute, successfully unveiled that the Asian wild rice (O. rufipogon Griff.) dramatically had increased grain yields with mutations at three genes in an initial step of domestication.

The loss of seed-shattering behaviour is an important step of domestication enabling humans to harvest more grains. At first, to experimentally reproduce an earlier process of rice domestication, several domestication-related genes were replaced with those of cultivated rice in the genetic background of wild rice, O. rufipogon. The replacement alone with a cultivated rice-type mutation of sh4, a rice gene with a major impact on seed shattering, was insufficient, but the replacement with cultivated rice-type mutations of both sh4 and qSH3, an allele within the seed-shattering gene OsSh1, caused the partial loss of abscission layer formation in O. rufipogon. However, the combination of two mutations of sh4 and qSH3 was not sufficient to increase yield under natural conditions. To further increase yield, our group found that the replacement together with cultivated rice-type mutations of three genes, sh4, qSH3 and SPR3, dramatically increased yields (Fig. 1). SPR3 is a rice gene controlling a panicle shape, and the closed panicle property enhances long awn-retaining seeds entangled, and in addition, reduces a bending moment which is a predominant factor affecting seed dispersal (Fig. 2), resulting in increased harvests.

We propose a stepwise route in the earliest phase of rice domestication, in which SPR3-controlled closed panicle morphology was instrumental in addition to sequential recruitments of sh4- and qSH3-dependent loss of shattering.

This study was supported partly by NIG-JOINT program 83A2016-2018. The wild rice accession, maintained by NIG in the support of National Bioresource Project (NBRP) Rice, was used in this study.

Inoue Group / Human Genetics Laboratory

Detection of Ancient Viruses and Long-Term Viral Evolution

Luca Nishimura, Naoko Fujito, Ryota Sugimoto, and Ituro Inoue*

Viruses (2022) 14, 1336 DOI:10.3390/v14061336

Archaeological remains contain Ancient DNA and RNA, and those nucleic acids provide genomic information about ancient people together with ancient microbiomes and viruses that infected ancient individuals. Since 1997, more than 20 ancient viral species including influenza virus and hepatitis B virus have been discovered from historical samples such as bones and mummified tissues. Those ancient viral genomes have been utilized to estimate the past pandemics of pathogenic viruses within the ancient human population and long-term evolutionary events. In our review article, we overview the ancient viral studies and experimental and analytical techniques and discuss the long-term viral evolutionary studies using ancient viral genomes.

Maeshima Group / Genome Dynamics Laboratory

Chromatin behavior in living cells: lessons from single-nucleosome imaging and tracking

*Satoru Ide, Sachiko Tamura, *Kazuhiro Maeshima *corresponding author

BioEssays 2022 June 03 DOI:10.1002/bies.202200043

Eukaryotic genome DNA is wrapped around core histones and forms a nucleosome structure. Together with associated proteins and RNAs, these nucleosomes are organized three-dimensionally in the cell as chromatin. Emerging evidence demonstrates that chromatin consists of rather irregular and variable nucleosome arrangements without the regular fiber structure and that its dynamic behavior plays a critical role in regulating various genome functions. Single-nucleosome imaging is a promising method to investigate chromatin behavior in living cells. It reveals local chromatin motion, which reflects chromatin organization not observed in chemically fixed cells. The motion data is like a gold mine. Data analyses from many aspects bring us more and more information that contributes to better understanding of genome functions. In this review article, we describe imaging of single-nucleosomes and their tracked behavior through oblique illumination microscopy. We also discuss applications of this technique, especially in elucidating nucleolar organization in living cells.

This work was supported by JSPS Grants and MEXT KAKENHI grants (21H02535, 20H05936 and 21H02453) and the Uehara Memorial Foundation.

Figure: Single-nucleosome imaging and tracking is a promising technique to investigate dynamic chromatin behavior in living cells. We describe how this imaging works using sparse nucleosome labeling and oblique illumination microscopy, and how information on chromatin dynamics can be extracted from the obtained motion data.

Video1: How laser beams traveled through a glass dish filled with medium using an oblique illumination microscopy. As the incident laser beam shifts from the center axis, higher refraction angles of the beam from the glass are obtained. At the last 2 frames, total internal reflection (TIR) occurs and only the glass surface is illuminated.

Video2: Movie data (50 ms/frame) of single nucleosomes （basic units of chromatin） fluorescently labeled in a living human cell. Note that clear, well-separated dots and their movements were visualized.

Single-nucleosome imaging reveals steady-state motion of interphase chromatin in living human cells

Shiori Iida, Soya Shinkai, Yuji Itoh, Sachiko Tamura, Masato T. Kanemaki, Shuichi Onami, Kazuhiro Maeshima

Science Advances (2022) 8, eabn5626 DOI:10.1126/sciadv.abn5626

Press release (In Japanese only)

The human body is composed of over forty trillion cells. Each of these cells has totally two meters of tightly packaged genomic DNA, the blueprint of life. Recently, there have been many advances in understanding how DNA is packaged and organized as chromatin in the cell. In contrast, how chromatin behaves in living cells remains unclear.

SOKENDAI graduate student Shiori Iida, JSPS Fellow Yuji Itoh, Technical Stuff Sachiko Tamura, and Professor Kazuhiro Maeshima of Genome Dynamics Laboratory (NIG), together with Research Scientist Soya Shinkai and Team Leader Shuichi Onami of RIKEN BDR, and Professor Masato T. Kanemaki of Molecular Cell Engineering Laboratory (NIG), have investigated the local movements of chromatin in living human cells using super-resolution fluorescence microscopy (Movie 1).

Both DNA amount and nuclear size become double during the preparation period for the cell division (interphase). Previously, it has been suggested that these drastic changes in the nuclear environment would affect chromatin movements. However, Iida et al. have revealed that chromatin motion keeps a steady state throughout the interphase. Chromatin motion is directly related to the accessibility of the DNA (readability of genomic information). Steady-state chromatin motion allows cells to conduct housekeeping tasks under similar environments during interphase.

This work was supported by JSPS and MEXT KAKENHI grants (20H05550、21H05763、19K23735、 20J00572、18H05412、19H05273、20H05936), a Japan Science and Technology Agency CREST grant (JPMJCR15G2), JST SPRING(JPMJSP2104), the Takeda Science Foundation, and the Uehara Memorial Foundation.

Figure: The swaying motion of chromatin keeps a steady state throughout the interphase (G1, S, G2 phases) despite increases in DNA amount and nuclear volume. Steady-state chromatin motion allows cells to conduct housekeeping tasks under similar environments during interphase.

Video1: Movie data (50 ms/frame) of single nucleosomes （basic units of chromatin） fluorescently labeled in a living human cell. Note that clear, well-separated dots and their movements were visualized.

Video2: Movie data (50 ms/frame) of single nucleosomes fluorescently labeled in living human cells; (left) G1-phase, (right) G2-phase. Note that there is not much difference in nucleosome motion between G1 and G2 phase, even as nuclear size increases.

▶ The article of EurekAlert! is here.