Abstract
Day length is an important environmental factor affecting the growth and development of maize (Zea mays), a short day (SD) plant grown in different latitudes. Leaf has been recognized as the light perceiving and signal producing organ. Under long day (LD) conditions, photoperiod-sensitive induction phase in maize begins at the fourth fully expanded leaf stage. However, the changes of maize leaf proteome in response to LD are largely unknown. To reveal maize proteome response to LD, proteins extracted from newly expanded fifth, sixth and seventh leaves from maize inbred line 496-10 (photoperiod sensitive) and Huangzao4 (HZ4, photoperiod insensitive) under LD treatments were compared via gel-based proteomic approach. As a result, eleven differentially expressed proteins were identified between 496-10 and HZ4 by mass spectrometry. This difference in protein accumulation was highly reproducible during the fifth to seventh leaf stages and most obvious at the seventh leaf stage. The identified proteins are mainly involved in circadian clock or iron metabolism, light harvesting and photosynthesis, nucleic acid metabolism and carbon fixation or energy metabolism. This study provides new insight into the influences of LD treatment on SD plants, such as maize, at proteome level.
Abbreviations
- Cab protein:
-
Chlorophyll a/b binding protein
- LD:
-
Long day
- HZ4:
-
Huangzao4
- RuBisCO:
-
Ribulose-1,5-bisphosphate carboxylase/oxygenase
- ROS:
-
Reactive oxygen species
- SOD:
-
Superoxide dismutase
- SD:
-
Short day
References
Betran FJ, Ribaut JM, Beck D, Gonzalez de León D (2003) Genetic diversity, specific combining ability, and heterosis in tropical maize under stress and nonstress environments. Crop Sci 43:797–806
Caliskan M (2000) Germin, an oxalate oxidase, has a function in many aspects of plant life. Turk J Biol 24:717–724
Cao W, Moss DN (1989) Daylength effect on leaf emergence and phyllochron in wheat and barley. Crop Sci 29:1021–1025
Coles ND, McMullen MD, Balint-Kurti PJ, Pratt RC, Holland JB (2010) Genetic control of photoperiod sensitivity in maize revealed by joint multiple population analysis. Genetics 184:799–812
Cook WB, Walker JC (1992) Identification of a maize nucleic acid-binding protein (NBP) belonging to a family of nuclear-encoded chloroplast proteins. Nucl Acids Res 20:359–364
Coruzzi G, Broglie R, Edwards C, Chua NH (1984) Tissue-specific and light-regulated expression of a pea nuclear gene encoding the small subunit of ribulose-1, 5-bisphosphate carboxylase. EMBO J 3:1671
Hayama R, Coupland G (2004) The molecular basis of diversity in the photoperiodic flowering responses of Arabidopsis and rice. Plant Physiol 135:677–684
Jensen GR (2000) Activation of Rubisco regulates photosynthesis at high temperature and CO2. PNAS 97:12937–12938
Komiya R, Yokoi S, Shimamoto K (2009) A gene network for long-day flowering activates RFT1 encoding a mobile flowering signal in rice. Development 136:3443–3450
Kovács L, Damkjær J, Kereïche S, Ilioaia C, Ruban AV, Boekema EJ, Jansson S, Horton P (2006) Lack of the light-harvesting complex CP24 affects the structure and function of the grana membranes of higher plant chloroplasts. Plant Cell 18:3106–3120
Ku LX, Li SY, Chen X, Wu LC, Wang XT, Chen YH (2011) Cloning and characterization of putative Hd6 ortholog associated with Zea mays L. photoperiod sensitivity. Agr Sci China 10:18–27
Li XP, Björkman O, Shih C, Grossman AR, Rosenquist M, Jansson S, Niyogi KK (2000) A pigment-binding protein essential for regulation of photosynthetic light harvesting. Nature 403:391–395
Lu M, Han YP, Gao JG, Wang XJ, Li WB (2010) Identification and analysis of the germin-like gene family in soybean. BMC Genom 11:620
Metivier J, Viana AM (1979) The effect of long and short day length upon the growth of whole plants and the level of soluble proteins, sugars, and stevioside in leaves of Stevia rebaudiana Bert. J Exp Bot 30:1211–1222
Motohashi R, Yamazaki T, Myouga F, Ito T, Ito K, Satou M, Kobayashi M, Nagata N, Yoshida S, Nagashima A, Tanaka K, Takahashi S, Shinozaki K (2007) Chloroplast ribosome release factor 1 (AtcpRF1) is essential for chloroplast development. Plant Mol Biol 64:481–497
Ravet K, Touraine B, Boucherez B, Briat JF, Gaymard F, Cellier F (2009) Ferritins control interaction between iron homeostasis and oxidative stress in Arabidopsis. Plant J 57:400–412
Salome PA, Oliva M, Weigel D, Kramer U (2013) Circadian clock adjustment to plant iron status depends on chloroplast and phytochrome function. EMBO J 32:511–523
Shi YH, Wang CZ, Zhang WY, Wang XK, Yu XD (2009) Effects of photoperiod on activities of superoxide dismutase (SOD) and peroxidase (POD) in fall dormancy lucerne cv. Vernal. Chin J Grassland 31:107–110
Takabe T, Incharoensakdi A, Arakawa K, Yokota S (1988) CO2 fixation rate and RuBisCO content increase in the halotolerant cyanobacterium, Aphanothece halophytica, grown in high salinities. Plant Physiol 88:1120–1124
Wang Y, Lin A, Loake GJ, Chu CC (2013) H2O2-induced leaf cell death and the crosstalk of reactive nitric/oxygen species. J Integr Plant Biol 55:202–208
Wu LC, Wang TG, Ku LX, Huang QC, Sun ZH, Xia ZL, Chen YH (2008) Determination of the photoperiod-sensitive inductive phase in maize with leaf numbers and morphologies of stem apical meristem. Agr Sci China 7:554–560
Wu XL, Liu HY, Wang W, Chen SN, Hu XL, Li CH (2011) Proteomic analysis of seed viability in maize. Acta Physiol Plant 33:181–191
Wu XL, Xiong EH, Wang W, Scali M, Cresti M (2014) Universal sample preparation method integrating trichloroacetic acid/acetone precipitation with phenol extraction for crop proteomic analysis. Nat Protoc 9:362–374
Yang Q, Li Z, Li WQ, Ku LX, Ye JR, Li K, Yang N, Li YP, Zhong T, Li JS, Chen YH, Yan JB, Yang XH, Xu ML (2013) CACTA-like transposable element in ZmCCT attenuated photoperiod sensitivity and accelerated the post domestication spread of maize. PNAS 110:16969–16974
Zhang SH, Shi DQ, Xu JS, Yang YF, Kang JW, Wang LM (1995) Effects of mass selection on adaptive improvement of exotic quality protein maize population. I. Direct response to selection for early silking. Acta Agron Sin 21:271–280
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This work was supported by the Ministry of Science and Technology of China (grant no. 2011CB111509).
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Communicated by M. Stobiecki.
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Wang, N., Ku, L., Chen, Y. et al. Comparative proteomic analysis of leaves between photoperiod-sensitive and photoperiod-insensitive maize inbred seedlings under long day treatments. Acta Physiol Plant 37, 1705 (2015). https://doi.org/10.1007/s11738-014-1705-7
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DOI: https://doi.org/10.1007/s11738-014-1705-7