| 000 | 03646nab a22003737a 4500 | ||
|---|---|---|---|
| 001 | 64731 | ||
| 003 | MX-TxCIM | ||
| 005 | 20211217230304.0 | ||
| 008 | 200115s2018 sz |||p|op||| 00| 0 eng d | ||
| 022 | _a1422-0067 (Online) | ||
| 024 | 8 | _ahttps://doi.org/10.3390/ijms19103225 | |
| 040 | _aMX-TxCIM | ||
| 041 | _aeng | ||
| 100 | 1 |
_926056 _aZenda, T. |
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| 245 | 1 | 0 | _aComparative proteomic and physiological analyses of two divergent maize inbred lines provide more insights into drought-stress tolerance mechanisms |
| 260 |
_aBasel (Switzerland) : _bMDPI, _c2018. |
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| 500 | _aPeer review | ||
| 500 | _aOpen Access | ||
| 520 | _aDrought stress is the major abiotic factor threatening maize (Zea mays L.) yield globally. Therefore, revealing the molecular mechanisms fundamental to drought tolerance in maize becomes imperative. Herein, we conducted a comprehensive comparative analysis of two maize inbred lines contrasting in drought stress tolerance based on their physiological and proteomic responses at the seedling stage. Our observations showed that divergent stress tolerance mechanisms exist between the two inbred-lines at physiological and proteomic levels, with YE8112 being comparatively more tolerant than MO17 owing to its maintenance of higher relative leaf water and proline contents, greater increase in peroxidase (POD) activity, along with decreased level of lipid peroxidation under stressed conditions. Using an iTRAQ (isobaric tags for relative and absolute quantification)-based method, we identified a total of 721 differentially abundant proteins (DAPs). Amongst these, we fished out five essential sets of drought responsive DAPs, including 13 DAPs specific to YE8112, 107 specific DAPs shared between drought-sensitive and drought-tolerant lines after drought treatment (SD_TD), three DAPs of YE8112 also regulated in SD_TD, 84 DAPs unique to MO17, and five overlapping DAPs between the two inbred lines. The most significantly enriched DAPs in YE8112 were associated with the photosynthesis antenna proteins pathway, whilst those in MO17 were related to C5-branched dibasic acid metabolism and RNA transport pathways. The changes in protein abundance were consistent with the observed physiological characterizations of the two inbred lines. Further, quantitative real-time polymerase chain reaction (qRT-PCR) analysis results confirmed the iTRAQ sequencing data. The higher drought tolerance of YE8112 was attributed to: activation of photosynthesis proteins involved in balancing light capture and utilization; enhanced lipid-metabolism; development of abiotic and biotic cross-tolerance mechanisms; increased cellular detoxification capacity; activation of chaperones that stabilize other proteins against drought-induced denaturation; and reduced synthesis of redundant proteins to help save energy to battle drought stress. These findings provide further insights into the molecular signatures underpinning maize drought stress tolerance. | ||
| 546 | _aText in English | ||
| 650 | 7 |
_2AGROVOC _918275 _aProteomics |
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| 650 | 7 |
_2AGROVOC _91224 _aProteins |
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| 650 | 7 |
_2AGROVOC _91081 _aDrought stress |
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| 650 | 7 |
_2AGROVOC _926057 _aPhysiological response |
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| 650 | 7 |
_2AGROVOC _91314 _aZea mays |
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| 700 | 0 |
_926058 _aSongtao Liu |
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| 700 | 0 |
_926059 _aXuan Wang |
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| 700 | 0 |
_926060 _aHongyu Jin |
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| 700 | 0 |
_926061 _aGuo Liu |
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| 700 | 0 |
_926062 _aHuijun Duan |
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| 773 | 0 |
_dBasel (Switzerland) : MDPI, 2018. _gv. 19, no. 10, art. 3225 _tInternational Journal of Molecular Sciences _w57216 _x1422-0067 |
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| 856 | 4 |
_yClick here to access online _uhttps://doi.org/10.3390/ijms19103225 |
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_2ddc _cJA _n0 |
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_c64731 _d64723 |
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