Transcriptome Analysis of Rice Root Tips Reveals Auxin, Gibberellin and Ethylene Signaling Underlying Nutritropism

Author:

Yamazaki Kiyoshi1ORCID,Ohmori Yoshihiro1,Takahashi Hirokazu2,Toyoda Atsushi3ORCID,Sato Yutaka4ORCID,Nakazono Mikio2ORCID,Fujiwara Toru1

Affiliation:

1. Department of Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo , Yayoi, Bunkyo-ku, Tokyo, 113-8657 Japan

2. Graduate School of Bioagricultural Sciences, Nagoya University , Furo-cho, Chikusa, Nagoya, 464-8601 Japan

3. Advanced Genomics Center, National Institute of Genetics , Mishima, Shizuoka, 411-8540 Japan

4. Department of Genomics and Evolutionary Biology, National Institute of Genetics , Mishima, Shizuoka, 411-8540 Japan

Abstract

Abstract Nutritropism is a positive tropism toward nutrients in plant roots. An NH4+ gradient is a nutritropic stimulus in rice (Oryza sativa L.). When rice roots are exposed to an NH4+ gradient generated around nutrient sources, root tips bend toward and coil around the sources. The molecular mechanisms are largely unknown. Here, we analyzed the transcriptomes of the inside and outside of bending root tips exhibiting nutritropism to reveal nutritropic signal transduction. Tissues facing the nutrient sources (inside) and away (outside) were separately collected by laser microdissection. Principal component analysis revealed distinct transcriptome patterns between the two tissues. Annotations of 153 differentially expressed genes implied that auxin, gibberellin and ethylene signaling were activated differentially between the sides of the root tips under nutritropism. Exogenous application of transport and/or biosynthesis inhibitors of these phytohormones largely inhibited the nutritropism. Thus, signaling and de novo biosynthesis of the three phytohormones are necessary for nutritropism. Expression patterns of IAA genes implied that auxins accumulated more in the inside tissues, meaning that ammonium stimulus is transduced to auxin signaling in nutritropism similar to gravity stimulus in gravitropism. SAUR and expansin genes, which are known to control cell wall modification and to promote cell elongation in shoot gravitropism, were highly expressed in the inside tissues rather than the outside tissues, and our transcriptome data are unexplainable for differential elongation in root nutritropism.

Funder

Ministry of Education, Culture, Sports, Science and Technology

Plant-Structure Optimization Strategy

KAKENHI

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science,Physiology,General Medicine

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