TY - JOUR
T1 - LONG GRAIN 1
T2 - a novel gene that regulates grain length in rice
AU - Morita, Ryouhei
AU - Ichida, Hiroyuki
AU - Ishii, Kotaro
AU - Hayashi, Yoriko
AU - Abe, Hiroshi
AU - Shirakawa, Yuki
AU - Ichinose, Katsunori
AU - Tsuneizumi, Kazuhide
AU - Kazama, Tomohiko
AU - Toriyama, Kinya
AU - Sato, Tadashi
AU - Abe, Tomoko
N1 - Funding Information:
The ion beam-irradiation experiments were conducted at RIBF, operated by the RIKEN Nishina Center and the Center for Nuclear Study at the University of Tokyo. We thank Drs. Hidetaka Kaya and Seiichi Toki (National Agriculture and Food Research Organization; NARO) for providing the plasmids pOsU6-sgRNA-Sa and pZD202-SaCas9 for CRISPR/Cas9 genome editing experiments. We are grateful to the Support Unit for Bio-Material Analysis, and the Research Resources Division, RIKEN Center for Brain Science, for technical assistance with sequencing analysis. This study was partly supported by the Social Infrastructure Technology Development Program of RIKEN, the “Funding Program for Next Generation World-Leading Researchers (NEXT Program)” of the Japan Society for the Promotion of Science (GR096), and the Cross-ministerial Strategic Innovation Promotion Program (SIP) “Technologies for creating next-generation agriculture, forestry and fisheries” (funding agency: Bio-oriented Technology Research Advancement Institution, NARO). We thank Robert McKenzie, PhD, from Edanz Group ( www.edanzediting.com/ac ), for editing a draft of this manuscript.
Funding Information:
The ion beam-irradiation experiments were conducted at RIBF, operated by the RIKEN Nishina Center and the Center for Nuclear Study at the University of Tokyo. We thank Drs. Hidetaka Kaya and Seiichi Toki (National Agriculture and Food Research Organization; NARO) for providing the plasmids pOsU6-sgRNA-Sa and pZD202-SaCas9 for CRISPR/Cas9 genome editing experiments. We are grateful to the Support Unit for Bio-Material Analysis, and the Research Resources Division, RIKEN Center for Brain Science, for technical assistance with sequencing analysis. This study was partly supported by the Social Infrastructure Technology Development Program of RIKEN, the ?Funding Program for Next Generation World-Leading Researchers (NEXT Program)? of the Japan Society for the Promotion of Science (GR096), and the Cross-ministerial Strategic Innovation Promotion Program (SIP) ?Technologies for creating next-generation agriculture, forestry and fisheries? (funding agency: Bio-oriented Technology Research Advancement Institution, NARO). We thank Robert McKenzie, PhD, from Edanz Group (www.edanzediting.com/ac), for editing a draft of this manuscript. TA, TS, RM, and HI conceived and designed the research. TS, TK, and K Toriyama maintained plants in the paddy field and measured agronomic traits. RM, HI, K Ishii, YH, HA, YS, K Ichinose, and K Tuneizumi conducted the experiments. RM, HI, YH, and TA analyzed the data. RM, HI, YH, and TA wrote the manuscript. All authors read and approved the manuscript.
Publisher Copyright:
© 2019, Springer Nature B.V.
PY - 2019/9/1
Y1 - 2019/9/1
N2 - Grain size is one of the most important traits that influence grain yield in rice. Here we report the isolation and characterization of the long grain1 (lin1) mutant, which exhibited long grains and increased grain weight. A field trial conducted over 2 years indicated that the grain weight increased 3.0–6.6% in the lin1 mutant compared with that of the wild-type Nipponbare. Whole-genome sequencing and genetic linkage analysis indicated that a 1-bp deletion within the coding sequence of Os06g0675200, which showed no homology to previously characterized genes, is responsible for the lin1 phenotype. Quantitative real-time PCR indicated that LIN1 transcripts were more abundant in young panicles than at advanced inflorescence developmental stages, which indicated that LIN1 controls grain length mainly at early stages of grain development. Sequence polymorphism analysis of LIN1 showed that all 15 temperate japonica cultivars tested as well as six out of the nine indica cultivars tested possessed the Nipponbare-type LIN1 allele, whereas the remaining three indica cultivars and one aus cultivar tested harbored an identical missense mutation in LIN1. These results revealed that the mutant allele of LIN1 has not been widely utilized in breeding temperate japonica cultivars currently in cultivation. Our findings indicate that the lin1 mutation may be useful to further improve grain length and presumably grain yield in temperate japonica and indica rice cultivars that harbor the Nipponbare-type LIN1 allele.
AB - Grain size is one of the most important traits that influence grain yield in rice. Here we report the isolation and characterization of the long grain1 (lin1) mutant, which exhibited long grains and increased grain weight. A field trial conducted over 2 years indicated that the grain weight increased 3.0–6.6% in the lin1 mutant compared with that of the wild-type Nipponbare. Whole-genome sequencing and genetic linkage analysis indicated that a 1-bp deletion within the coding sequence of Os06g0675200, which showed no homology to previously characterized genes, is responsible for the lin1 phenotype. Quantitative real-time PCR indicated that LIN1 transcripts were more abundant in young panicles than at advanced inflorescence developmental stages, which indicated that LIN1 controls grain length mainly at early stages of grain development. Sequence polymorphism analysis of LIN1 showed that all 15 temperate japonica cultivars tested as well as six out of the nine indica cultivars tested possessed the Nipponbare-type LIN1 allele, whereas the remaining three indica cultivars and one aus cultivar tested harbored an identical missense mutation in LIN1. These results revealed that the mutant allele of LIN1 has not been widely utilized in breeding temperate japonica cultivars currently in cultivation. Our findings indicate that the lin1 mutation may be useful to further improve grain length and presumably grain yield in temperate japonica and indica rice cultivars that harbor the Nipponbare-type LIN1 allele.
UR - http://www.scopus.com/inward/record.url?scp=85071680270&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85071680270&partnerID=8YFLogxK
U2 - 10.1007/s11032-019-1032-1
DO - 10.1007/s11032-019-1032-1
M3 - Article
AN - SCOPUS:85071680270
SN - 1380-3743
VL - 39
JO - Molecular Breeding
JF - Molecular Breeding
IS - 9
M1 - 135
ER -