DEP2

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Annotated Information

Function

  • DEP2 gene reduced the development in the longitudinal direction but enhanced the development in the lateral direction of plural organs in rice. In the DEP2 mutants,the panicle length was reduced and panicle diameter was increased[1].
  • Besides panicle erectness, the DEP2 mutants also showed a slight reduction in plant height , an obvious decrease in panicle length, and a significant increase in both rachis and stem diameter. The leaves of DEP2 are short, wide, and erect, and the overall appearance of the mutant is more compact. The grain density is increased due to the decreased panicle length but not the change of grain number. The grains of the DEP2 mutant are wider and shorter than the wild type[1].
  • The mutation in DEP2 has pleiotropic effects on plant architecture,and that increased diameter of the rachis and decreased panicle length altogether contributed to the dense and erect panicle phenotype[1].
  • The DEP2 gene may regulate GA synthesis, and mutation of DEP2 leads to a decrease in plant height[1].
Map-based cloning of the DEP2 gene(from reference.[1].)

Mutation

  • The DEP2 locus was mapped to the long arm of rice chromosome 7[1].

dep2-1:The 31-bp deletion in dep2-1 starts at 2184bp from the initiation codon ATG and caused a frameshift; dep2-2:the G/A substitution in the second intron of dep2-2 caused an altered splicing site of the second intron and also led to a frameshift. LOC_Os07g42410 was considered a candidate for the DEP2 gene[1].

DEP2 expression pattern[1]

Expression

  • DEP2 gene expression in the dividing zones of rachis, branches, and florets was higher than in other parts of the rice plant.
  • This gene is highly expressed in young panicles ranging from 1 to 15 cm in length;low level expression was also detected in the other organs, including roots,stems,leaves and leaf sheathes.

Evolution

  • DEP2 may be a plant-specific protein. The only existing low similarity to CIP7 in Arabidopsis is found at the N terminal part of the protein, while the COP1-interacting motif, transcription activation domain, and the nuclear localization signal domain are all missing in DEP2.

Knowledge extension

  • Except dep2,cl7(t) was a novel allele of dep2. Sequence analysis showed that cl7(t) had a single nucleotide substitution (C to A) in the third exon that leads to a Ser substitution with a stop codon, giving a truncated DEP2 protein.
  • The leaves of the cl7(t) mutant were shorter with a smaller angle between the leaves and stem, and a higher chlorophyll content than that of wild type. Compared with the wild type, the cl7(t) mutant displayed a 30% reduction in panicle length and a marked decrease in the number of grains per panicle. the grains of the mutant were wider and shorter than those of the wild type.

Labs working on this gene

  • Rice Research Institute, Anhui Academy of Agricultural Sciences, Hefei 230031, PR China
  • Key Laboratory of Ion Beam Bioengineering, Institute of Technical Biology and Agriculture Engineering, Chinese Academy of Sciences,Hefei 230031, PR China
  • Key Laboratory of Resource Plant Biology of Anhui Province, College of Life Sciences, Huaibei Normal University, Huaibei 235000,PR China
  • Institute of Agricultural Engineering, Anhui Academy of Agricultural Sciences, Hefei 230031, PR China
  • College of Life Sciences, Anhui Agricultural University, Hefei 230031, Anhui, PR China
  • State Key Laboratory of Plant Genomics and National Center for Plant Gene Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China
  • Graduate School of the Chinese Academy of Sciences, Beijing 100101, China
  • Department of Bioscience,Fukui Prefectural University,4-1-1 Matsuoka Kenjyojima,Eiheiji-cho,Yoshida-gun,Fukui 910-1195,Japan
  • Institute of Society for Techno-innovation of Agricuture,Forestry and Fisheries.Tsukuba,Ibaraki 305-0854,Japan
  • QTL Genomics Research Center,National Institute of Agrobiological Sciences,Tsukuba,Ibaraki 305-8602,Japan
  • Bioscience and Biotechnology Center,Nagoya University,Chikusa,Nagoya 464-8604,Japan

References

<references> [2] [3] [1]

Feng Li,Wenbo Liu, Jiuyou Tang, Jinfeng Chen,et al.(2010)Rice DENSE AND ERECT PANICLE 2 is essential for determining panicle outgrowth and elongation.Cell Research 20:838-849.</ref>

[3]
  1. ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 Kunihiro S, Saito T, Matsuda T, et al. Rice DEP1, encoding a highly cysteine-rich G protein γ subunit, confers cadmium tolerance on yeast cells and plants[J]. Journal of experimental botany, 2013, 64(14): 4517-4527.
  2. ↑ Huang X, Qian Q, Liu Z, et al. Natural variation at the DEP1 locus enhances grain yield in rice[J]. Nature genetics, 2009, 41(4): 494-497.
  3. ↑ 3.0 3.1 Sun H, Qian Q, Wu K, et al. Heterotrimeric G proteins regulate nitrogen-use efficiency in rice[J]. Nature genetics, 2014. Cite error: Invalid <ref> tag; name "ref2" defined multiple times with different content
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