Reference "Expression of a betaine aldehyde dehydrogenase gene in rice, a glycinebetaine nonaccumulator, and possible localization of its protein in peroxisomes"

Reference ID

3072

Title

Expression of a betaine aldehyde dehydrogenase gene in rice, a glycinebetaine nonaccumulator, and possible localization of its protein in peroxisomes

Source

The Plant journal : for cell and molecular biology, 1997, vol. 11, pp. 1115-1120

Authors (7)

Nakamura-T	Yokota-S
Muramoto-Y	Tsutsui-K
Oguri-Y	Fukui-K
Takabe-T

Abstract

Betaine aldehyde dehydrogenase (BADH) catalyzes the last step in the plant
biosynthetic pathway that leads to glycinebetaine. Rice plants (Oryza sativa
L.), albeit considered a typical non-glycinebetaine accumulating species, have
been found to express this enzyme at low levels. This observation evokes an
interest in phylogenic evolution of the enzyme in the plant kingdom. It is
reported here that rice plants possess the ability to take up exogenously added
betaine aldehyde through the roots and convert it to glycinebetaine, resulting
in an enhanced salt-tolerance of the plants. A gene encoding a putative BADH
from the rice genome was also cloned and sequenced. The gene was found to
contain 14 introns, and the overall nucleotide sequence of the coding region is
c. 78% identical to that of the barley BADH cDNA. Cloning of a partial BADH cDNA
from rice was accomplished by reverse transcription-polymerase chain reaction
(RT-PCR). The nucleotide sequence of the cloned fragment was found to be
identical to the corresponding exon regions of the rice genomic BADH gene. The
deduced amino acid sequences of rice and barley BADH both contain a C-terminal
tripeptide SKL, a signal known to target preproteins to microbodies. This
localization was confirmed by an immuno-gold labeling study of transgenic
tobacco harboring barley cDNA, which showed BADH protein inside peroxisomes.
Northern blot analysis revealed that the level of BADH mRNA is salt-inducible.