4.8 Article

Specific changes in total and mitochondrial proteomes are associated with higher levels of heterosis in maize hybrids

Journal

PLANT JOURNAL
Volume 72, Issue 1, Pages 70-83

Publisher

WILEY-BLACKWELL
DOI: 10.1111/j.1365-313X.2012.05056.x

Keywords

Zeamays; heterosis; proteomics; mitochondria; 2D DIGE; label-free MS

Categories

Funding

  1. National Science Foundation, Division of Biological Infrastructure (NSF-DBI) [0922769]
  2. Division Of Integrative Organismal Systems
  3. Direct For Biological Sciences [0922769] Funding Source: National Science Foundation

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The phenomenon of hybrid vigor (heterosis) has long been harnessed by plant breeders to improve world food production. However, the changes that are essential for heterotic responses and the mechanisms responsible for heterosis remain undefined. Large increases in biomass and yield in high-heterosis hybrids suggest that alterations in bioenergetic processes may contribute to heterosis. Progeny from crosses between various inbred lines vary in the extent of vigor observed. Field-grown maize F1 hybrids that consistently exhibited either low or high heterosis across a variety of environments were examined for changes in proteins that may be correlated with increased plant vigor and yield. Unpollinated ears at the time of flowering (ear shoots) were selected for the studies because they are metabolically active, rich in mitochondria, and the sizes of the ears are diagnostic of yield heterosis. Total protein and mitochondrial proteomes were compared among low- and higher-heterosis hybrids. Two-dimensional difference gel electrophoresis was used to identify allelic and/or isoform differences linked to heterosis. Identification of differentially regulated spots by mass spectrometry revealed proteins involved in stress responses as well as primary carbon and protein metabolism. Many of these proteins were identified in multiple spots, but analysis of their abundances by label-free mass spectrometry suggested that most of the expression differences were due to isoform variation rather than overall protein amount. Thus, our proteomics studies suggest that expression of specific alleles and/or post-translational modification of specific proteins correlate with higher levels of heterosis.

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