Barley dormancy mutation suggests beer motivated early farmers
Okayama University have identified the gene mutation and the enzyme it encodes to determine whether the dormancy of barley is long (better for food crops) or short (better for beer-making).
|Effects of qsd1 (left) and Qsd1 (right) alleles on seed germination after five weeks of 25° C dormancy |
reduction treatment [Credit: Okayama University]
Kazuhiro Sato and colleagues – a collaboration of Okayama University and the Institute of Agrobiological Sciences in Japan and the University of Adelaide in Australia - compared DNA sequences of Haruna Nijo – a type of barley known to have short dormancy – with wild barley H602, known to have long dormancy. After studying over 5000 plants, they identified the section of the barley's DNA that varies with expression of long or short dormancy - AK372829.
The gene AK372829 codes the enzyme alanine aminotransferase (AlaAT), which is known to play a pivotal role in nitrogen and carbon pathways and protein synthesis, and has been implicated in stress responses to low oxygen and nitrogen availability. Further experiments investigated variations in the nucleotide – that is, single nucleotide polymorphisms (SNPs) – as well as the structure and diversity of the protein associated with short dormancy.
Haruna Nijo has a dominant short dormancy allele Qsd1, whereas H602 has a recessive long dormancy allele qsd1. The results indicate that Haruna Nijo shares ancestry from long dormancy food-producing barley, suggesting "specific selection of reduced dormancy for the malting process". As the researchers conclude in their report of the work, the selection and exploitation of the plants expressing the Qsd1 mutation for short dormancy "contributes further to the debate as to what extent the development of ancient agrarian societies was driven by the human appetite for flour and bread, or for beer and alcohol."
The findings are published in Nature Communications.
Source: Okayama University [November 24, 2016]