TY - JOUR
T1 - The HKM gene, which is identical to the MS1 gene of Arabidopsis thaliana, is essential for primexine formation and exine pattern formation
AU - Ariizumi, Tohru
AU - Hatakeyama, Katsunori
AU - Hinata, Kokichi
AU - Sato, Shusei
AU - Kato, Tomohiko
AU - Tabata, Satoshi
AU - Toriyama, Kinya
N1 - Funding Information:
Acknowledgements We are grateful to Dr. Takuya Ito and Dr. Kazuo Shinozaki for providing the ms1-8 mutant. We are grateful to Dr. Kara Johnson in the Department of Crop and Soil Science of Washington State University for critical reading of the manuscript. This work was supported by a grant-in-aid from the Ministry of Education, Culture, Sports, Science and 18 Technology of Japan and the Research for the Future Program of the Japan Society for the Promotion of Science (JSPS=RFTF00L01606). T.A. is a recipient of a Research Fellowship for young scientists from JSPS.
PY - 2005/6
Y1 - 2005/6
N2 - A male-sterile mutant of Arabidopsis thaliana was isolated by T-DNA tagging screening. Using transmission electron microscopy analysis, we revealed that the microspores of this mutant did not have normal thick primexine on the microspore at the tetrad stage. Instead, a moderately electron-dense layer formed around the microspores. Although microspores without normal primexine failed to form a proper reticulate exine pattern at later stages, sporopollenin was deposited and an exine-like hackly structure was observed on the microspores during the microspore stage. Thus, this mutant was named hackly microspore (hkm). It is speculated that the moderately electron-dense layer was primexine, which partially played its role in sporopollenin deposition onto the microspore. Cytological analysis revealed that the tapetum of the hkm mutant was significantly vacuolated, and that vacuolated tapetal cells crushed the microspores, resulting in the absence of pollen grains within the anther at anthesis. Single nucleotide polymorphism analysis demonstrated that the hkm mutation exists within the MS1 gene, which has been reportedly expressed within the tapetum. Our results suggest that the critical process of primexine formation is under sporophytic control.
AB - A male-sterile mutant of Arabidopsis thaliana was isolated by T-DNA tagging screening. Using transmission electron microscopy analysis, we revealed that the microspores of this mutant did not have normal thick primexine on the microspore at the tetrad stage. Instead, a moderately electron-dense layer formed around the microspores. Although microspores without normal primexine failed to form a proper reticulate exine pattern at later stages, sporopollenin was deposited and an exine-like hackly structure was observed on the microspores during the microspore stage. Thus, this mutant was named hackly microspore (hkm). It is speculated that the moderately electron-dense layer was primexine, which partially played its role in sporopollenin deposition onto the microspore. Cytological analysis revealed that the tapetum of the hkm mutant was significantly vacuolated, and that vacuolated tapetal cells crushed the microspores, resulting in the absence of pollen grains within the anther at anthesis. Single nucleotide polymorphism analysis demonstrated that the hkm mutation exists within the MS1 gene, which has been reportedly expressed within the tapetum. Our results suggest that the critical process of primexine formation is under sporophytic control.
KW - Arabidopsis thaliana
KW - Exine
KW - Male sterility
KW - Primexine
KW - Tapetum
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U2 - 10.1007/s00497-005-0242-3
DO - 10.1007/s00497-005-0242-3
M3 - Article
AN - SCOPUS:21344435964
SN - 2194-7953
VL - 18
SP - 1
EP - 7
JO - Plant Reproduction
JF - Plant Reproduction
IS - 1
ER -