TY - CHAP
T1 - Improving oat Beta-glucan content by biotechnological methods
AU - Kiviharju, E.
AU - Ritala, Anneli
AU - Tanhuanpää, P.
AU - Kalendar, R.
AU - Manninen, O.
AU - Suortti, Tapani
AU - Hietaniemi, V.
AU - Pietilä, L.
AU - Oksman-Caldentey, Kirsi-Marja
AU - Nuutila, Anna-Maria
AU - Schulman, A.
PY - 2007
Y1 - 2007
N2 - Oat (Avena sativa L.) products lower the blood cholesterol level, a
risk factor in heart diseases. Moreover, Beta-glucan also helps to normalize
the postprandial blood glucose level and reduces the risk of colon cancer.
These health benefits are mainly associated with high levels of mixed-linked
(1,3)-(1,4)-Beta-D-glucan, a dietary fiber of which the main part is
soluble. The amount of Beta-glucan is dependent on the genotype and thus can
be increased by cultivar breeding. In this study, modern biotechnology tools
were applied in order to breed high Beta-glucan oat cultivars for food and
processing purposes. To understand the inheritance of Beta-glucan content in
oat and to enable DNA-marker-assisted selection in oat cultivar breeding, a
genetic linkage map was constructed for a Nordic oat cross. An Aslak x
Matilda mapping population of 137 totally homozygous DH-lines was produced
by anther culture. The linkage map consisted of over 600 PCR-based
DNA-markers, including microsatellites, RAPDs, REMAPs, ISSRs, SRAPs and
AFLPs. The QTL analysis showed two QTLs associated with Beta-glucan content.
Together they explained about 37% of the variation in the DH lines. In both
chromosomal regions alleles from Aslak had a favorable effect on Beta-glucan
content. On the basis of the results, markers tightly linked to the genes
themselves may be developed for DNA-marker assisted selection of high
Beta-glucan content containing oat breeding lines. QTLs were located also
for other traits of interest. Another aim was to modify the Beta-glucan
content of Finnish oat cultivars through genetic engineering. Embryogenic
cell cultures were started from mature embryos of oat cultivars Aslak, Veli,
and Kolbu. A microbial 1,3-Beta-glucan synthase was transferred to oat cell
lines by particle bombardment and transgenic plants were regenerated. The
expression of the microbial gene in transgenic cell cultures was
demonstrated by semi-quantitative RT-PCR. The 1,3-1,4-beta-glucan amounts
were reduced and the molecular weight of the mixed-linked Beta-glucan
differed in some transgenic seed lines when compared to non-transgenic
control seeds. The analyses of 1,3-beta-glucan contents of transgenic cell
lines and seeds is ongoing. A basis exists for modifying oat Beta-glucan
contents through genetic engineering.
AB - Oat (Avena sativa L.) products lower the blood cholesterol level, a
risk factor in heart diseases. Moreover, Beta-glucan also helps to normalize
the postprandial blood glucose level and reduces the risk of colon cancer.
These health benefits are mainly associated with high levels of mixed-linked
(1,3)-(1,4)-Beta-D-glucan, a dietary fiber of which the main part is
soluble. The amount of Beta-glucan is dependent on the genotype and thus can
be increased by cultivar breeding. In this study, modern biotechnology tools
were applied in order to breed high Beta-glucan oat cultivars for food and
processing purposes. To understand the inheritance of Beta-glucan content in
oat and to enable DNA-marker-assisted selection in oat cultivar breeding, a
genetic linkage map was constructed for a Nordic oat cross. An Aslak x
Matilda mapping population of 137 totally homozygous DH-lines was produced
by anther culture. The linkage map consisted of over 600 PCR-based
DNA-markers, including microsatellites, RAPDs, REMAPs, ISSRs, SRAPs and
AFLPs. The QTL analysis showed two QTLs associated with Beta-glucan content.
Together they explained about 37% of the variation in the DH lines. In both
chromosomal regions alleles from Aslak had a favorable effect on Beta-glucan
content. On the basis of the results, markers tightly linked to the genes
themselves may be developed for DNA-marker assisted selection of high
Beta-glucan content containing oat breeding lines. QTLs were located also
for other traits of interest. Another aim was to modify the Beta-glucan
content of Finnish oat cultivars through genetic engineering. Embryogenic
cell cultures were started from mature embryos of oat cultivars Aslak, Veli,
and Kolbu. A microbial 1,3-Beta-glucan synthase was transferred to oat cell
lines by particle bombardment and transgenic plants were regenerated. The
expression of the microbial gene in transgenic cell cultures was
demonstrated by semi-quantitative RT-PCR. The 1,3-1,4-beta-glucan amounts
were reduced and the molecular weight of the mixed-linked Beta-glucan
differed in some transgenic seed lines when compared to non-transgenic
control seeds. The analyses of 1,3-beta-glucan contents of transgenic cell
lines and seeds is ongoing. A basis exists for modifying oat Beta-glucan
contents through genetic engineering.
M3 - Conference abstract in proceedings
SN - 978-951-38-6321-0
T3 - VTT Symposium
SP - 120
EP - 120
BT - Plants for Human Health in the Post-Genome Era
PB - VTT Technical Research Centre of Finland
CY - Espoo
T2 - PSE Congress: Plants for Human Health in the Post-Genome Era
Y2 - 26 August 2007 through 29 August 2007
ER -