Characterization and Fine Mapping of a Novel Rice Albino Mutant low temperature albino 1

Yu Peng; Yi Zhang; Jun Lv; Jianhui Zhang; Ping Li; Xiaoliang Shi; Yufeng Wang; Honglei Zhang; Zuhua He; Sheng Teng

doi:10.1016/j.jgg.2012.05.001

Volume 39 Issue 8

Aug. 2012

Turn off MathJax

Article Contents

Article Navigation > Journal of Genetics and Genomics > 2012 > 39(8): 385-396

PDF( 2018 KB)

Characterization and Fine Mapping of a Novel Rice Albino Mutant low temperature albino 1

doi: 10.1016/j.jgg.2012.05.001

a
Institute of Plant Physiology & Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China
b
College of Agronomy and Biotechnology, Southwest University, Chongqing 400715, China
c
College of Life and Environment Sciences, Shanghai Normal University, Shanghai 200234, China

More Information

Corresponding author: E-mail address: zhhe@sibs.ac.cn (Zuhua He); E-mail address: steng@sibs.ac.cn (Sheng Teng)
Received Date: 2012-02-19
Accepted Date: 2012-05-02
Rev Recd Date: 2012-04-29

Available Online: 2012-05-08

Publish Date: 2012-08-20

Abstract

Abstract

Albino mutants are useful genetic resource for studying chlorophyll biosynthesis and chloroplast development and cloning genes involved in these processes in plants. Here we report a novel rice mutant low temperature albino 1 (lta1) that showed albino leaves before 4-leaf stage when grown under temperature lower than 20°C, but developed normal green leaves under temperature higher than 24°C or similar morphological phenotypes in dark as did the wild-type (WT). Our analysis showed that the contents of chlorophylls and chlorophyll precursors were remarkably decreased in the lta1 mutant under low temperature compared to WT. Transmission electron microscope observation revealed that chloroplasts were defectively developed in the albino lta1 leaves, which lacked of well-stacked granum and contained less stroma lamellae. These results suggested that the lta1 mutation may delay the light-induced thylakoid assembly under low temperature. Genetic analysis indicated that the albino phenotype was controlled by a single recessive locus. Through map-based approach, we finally located theLta1 gene to a region of 40.3 kb on the short arm of chromosome 11. There are 8 predicted open reading frames (ORFs) in this region and two of them were deleted in lta1 genome compared with the WT genome. The further characterization of the Lta1 gene would provide a good approach to uncover the novel molecular mechanisms involved in chloroplast development under low temperature stress.
- Rice,
- Mutant,
- Chloroplast development,
- Gene mapping

FullText(HTML)

References(58)

References

[1]	Arnon, D.I. Plant Physiol., 24 (1949),pp. 1-15
[2]	Barry, J.P., Veronica, A. Genetic dissection of chloroplast biogenesis and development: an overview Plant Physiol., 155 (2010),pp. 1545-1551
[3]	Beale, S.I. Green genes gleaned Trends Plant Sci., 10 (2005),pp. 309-312
[4]	Blankenship, R.E.
[5]	Chateigner-Boutin, A.L., Ramos-Vega, M., Guevara-Garcia, A. Plant J., 56 (2008),pp. 590-602
[6]	Chen, M., Jensen, M., Rodermel, S. J. Hered., 90 (1999),pp. 207-214
[7]	Chen, M., Choi, Y., Voytas, D.F. et al. Plant J., 22 (2000),pp. 303-313
[8]	Chen, T., Zhang, Y.D., Zhao, L. et al. Physiological character and gene mapping in a new green-revertible albino mutant in rice J. Genet. Genomics, 34 (2007),pp. 331-338
[9]	Chen, T., Zhang, Y.D., Zhao, L. et al. J. Genet. Genomics, 36 (2009),pp. 117-123
[10]	Cornah, J.E., Terry, M.J., Smith, A.G. Green or red: what stops the traffic in the tetrapyrrole pathway Trends Plant Sci., 8 (2003),pp. 224-230
[11]	Damian, J.A., Donald, R.O. Impacts of chilling temperatures on photosynthesis in warm-climate plants Trends Plant Sci., 6 (2001),pp. 36-42
[12]	Dario, L. Chloroplast research in the genomic age Trend Genet., 19 (2003),pp. 47-56
[13]	David, B.S., Michel, G.C., Maureen, R.H. Chloroplast RNA metabolism Annu. Rev. Plant Biol., 61 (2010),pp. 125-155
[14]	Delannoy, E., Stanley, W.A., Bond, C.S. et al. Pentatricopeptide repeat (PPR) proteins as sequence-specificity factors in post-transcriptional processes in organelles Biochem. Soc. Trans, 35 (2007),pp. 1643-1647
[15]	Douzery, E.J., Snell, E.A., Bapteste, E. et al. The timing of eukaryotic evolution: does a relaxed molecular clock reconcile proteins and fossils? Proc. Natl. Acad. Sci. USA, 101 (2004),pp. 15386-15391
[16]	Dyall, S.D., Brown, M.T., Johnson, P.J. Ancient invasions: from endosymbionts to organelles Science, 304 (2004),pp. 253-257
[17]	Falcon de Longevialle, A., Hendrickson, L., Taylor, N.L. et al. Plant J., 56 (2008),pp. 157-168
[18]	Gothandam, K.M., Kim, E.S., Cho, H. et al. OsPPR1, a pentatricopeptide repeat protein of rice is essential for the chloroplast biogenesis Plant Mol. Biol., 58 (2005),pp. 421-433
[19]	Hajdukiewicz, P.T., Allison, L.A., Maliga, P. The two RNA polymerases encoded by the nuclear and the plastid compartments transcribe distinct groups of genes in tobacco plastids EMBO J., 16 (1997),pp. 4041-4048
[20]	Hattori, M., Miyake, H., Sugita, M. J. Biol. Chem., 282 (2007),pp. 10773-10782
[21]	He, G., Zhu, X., Elling, A.A. et al. Global epigenetic and transcriptional trends among two rice subspecies and their reciprocal hybrids Plant Cell, 22 (2010),pp. 17-33
[22]	Hodgins, R., Huystee, R.B. Rapid simultaneous estimation of protoporphyrin and Mg-protophyrins in higher plants J. Plant Physiol., 125 (1986),pp. 311-323
[23]	Ikeda, T.M., Gray, M.W. Characterization of a DNA-binding protein implicated in transcription in wheat mitochondria Mol. Cell. Biol., 19 (1999),pp. 8113-8122
[24]	Jung, K.H., Hur, J., Ryu, C.H. et al. Characterization of a rice chlorophyll-deficient mutant using the T-DNA gene-trap system Plant Cell Physiol., 44 (2003),pp. 463-472
[25]	Kong, M.M., Yu, Q.B., Zhang, H.Q. et al. Zhi Wu Sheng Li Yu Fen Zi Sheng Wu Xue Xue Bao, 32 (2006),pp. 433-437
[26]	Koseki, M., Kitazawa, N., Yonebayashi, S. et al. Identification and fine mapping of a major quantitative trait locus originating from wild rice, controlling cold tolerance at the seedling stage Mol. Genet. Genomics, 284 (2010),pp. 45-54
[27]	Kotera, E., Tasaka, M., Shikanai, T. A pentatricopeptide repeat protein is essential for RNA editing in chloroplasts Nature, 433 (2005),pp. 326-330
[28]	Koussevitzky, S., Nott, A., Mockler, T.C. et al. Signals from chloroplasts converge to regulate nuclear gene expression Science, 316 (2007),pp. 715-719
[29]	Kroeger, T.S., Watkins, K.P., Friso, G. et al. A plant-specific RNA-binding domain revealed through analysis of chloroplast group II intron splicing Proc. Natl. Acad. Sci. USA, 106 (2009),pp. 4537-4542
[30]	Kusumi, K., Mizutani, A., Nishimura, M. et al. Plant J., 12 (1997),pp. 1241-1250
[31]	Lander, E.S., Green, P., Abrahanson, J. et al. MAPMAKER: an interactive computing package for constructing primary genetic linkages of experimental and natural populations Genomics, 1 (1987),pp. 174-181
[32]	Lee, S., Kim, J.H., Yoo, E.S. et al. Plant Mol. Biol., 57 (2005),pp. 805-818
[33]	Liere, K., Maliga, P. EMBO J., 18 (1999),pp. 249-257
[34]	Lindahl, M., Spetea, C., Hundal, T. et al. The thylakoid FtsH protease plays a role in the light-induced turnover of the photosystem II D1 protein Plant Cell, 12 (2000),pp. 419-431
[35]	Lurin, C., Andres, C., Aubourg, S. et al. Plant Cell, 16 (2004),pp. 2089-2103
[36]	Meierhoff, K., Felder, S., Nakamura, T. et al. Plant Cell, 15 (2003),pp. 1480-1495
[37]	Mochizuki, N., Brusslan, J.A. Arabidopsis genomes uncoupled 5 (GUN5) mutant reveals the involvement of Mg-chelatase H subunit in plastid-to-nucleus signal transduction Proc. Natl. Acad. Sci. USA, 98 (2001),pp. 2053-2058
[38]	Okuda, K., Myouga, F., Motohashi, R. et al. Conserved domain structure of pentatricopeptide repeat proteins involved in chloroplast RNA editing Proc. Natl. Acad. Sci. USA, 104 (2007),pp. 8178-8183
[39]	Ostersetzer, O., Adam, Z. Light-stimulated degradation of an unassembled Rieske FeS protein by a thylakoid-bound protease: the possible role of the FtsH protease Plant Cell, 9 (1997),pp. 957-965
[40]	O'Toole, N., Hattori, M., Andres, C. et al. On the expansion of the pentatricopeptide repeat gene family in plants Mol. Biol. Evol., 25 (2008),pp. 1120-1128
[41]	Papenbrock, J., Mock, H.P., Tanaka, R. et al. Role of magnesium chelatase activity in the early steps of the tetrapyrrole biosynthetic pathway Plant Physiol., 122 (2000),pp. 1161-1170
[42]	Pfalz, J., Liere, K., Kandlbinder, A. et al. pTAC2, -6, and -12 are components of the transcriptionally active plastid chromosome that are required for plastid gene expression Plant Cell, 18 (2006),pp. 176-197
[43]	Sakamoto, W., Uno, Y., Zhang, Q. et al. Arrested differentiation of proplastids into chloroplasts in variegated leaves characterized by plastid ultrastructure and nucleoid morphology Plant Cell Physiol., 50 (2009),pp. 2069-2083
[44]	Sato, S., Nakamura, Y., Kaneko, T. et al. DNA Res., 6 (1999),pp. 283-290
[45]	Schmitz-Linneweber, C., Williams-Carrier, R.E., Williams-Voelker, P.M. et al. Plant Cell, 18 (2006),pp. 2650-2663
[46]	Shiina, T., Tsunoyama, Y., Nakahira, Y. et al. Plastid RNA polymerases, promoters, and transcription regulators in higher plants Int. Rev. Cytol., 244 (2005),pp. 1-68
[47]	Sugimoto, H., Kusumi, K., Tozawa, Y. et al. Plant Cell Physiol., 45 (2004),pp. 985-996
[48]	Sugimoto, H., Kusumi, K., Noguchi, K. et al. Plant J., 52 (2007),pp. 512-527
[49]	Sundqvist, C., Dahlin, C. With chlorophyll pigments from prolamellar bodies to light-harvesting complexes Physiol. Plantarum, 100 (1997),pp. 748-759
[50]	Susek, R.E., Ausubel, F.M. Cell, 74 (1993),pp. 787-799
[51]	Takechi, K.S., Murata, M., Motoyoshi, F. et al. Plant Cell Physiol., 41 (2000),pp. 1334-1346
[52]	Wang, Z.F., Wang, F.H., Zhou, R. et al. Euphytica, 181 (2011),pp. 405-413
[53]	Wu, Z., Zhang, X., He, B. et al. A chlorophyll-deficient rice mutant with impaired chlorophyllide esterification in chlorophyll biosynthesis Plant Physiol., 145 (2007),pp. 29-40
[54]	Xia, J.C., Wang, Y.P., Ma, B.T. et al. Acta Genetica Sinica, 33 (2006),pp. 1112-1119
[55]	Ye, J.W., Gong, Z.Y., Chen, C.G. et al. A mutation of OsOTP 51 leads to impairment of PS I complex assembly and serious photo-damage in rice J. Integr. Plant Biol, 54 (2012),pp. 87-98
[56]	Yoo, S.C., Cho, S.H., Sugimoto, H. et al. Plant Physiol., 150 (2009),pp. 388-401
[57]	Yu, Q.B., Jiang, H., Mi, H.L. et al. J. Shanghai Normal Uni. (Natural Sciences), 34 (2005),pp. 70-75
[58]	Zhou, W., Cheng, Y., Yap, A. et al. Plant J., 58 (2009),pp. 82-96