MTT Agrifood Research (http://www.mtt.fi/english/) of the
Finnish Ministry of Agriculture and Forestry produces scientific research and
develops new technology for the agriculture and food sectors.
Research at MTT covers biology, technology and agricultural economics, promotes the
competitiveness of the food industry, quality of the production environment and
the rural environment, the vitality of rural areas and their interaction with
urban areas, and consumer welfare. Its roots go back to 1898, when it was
established as an agricultural research centre.

Under the reorganisation of 2006, the Plant Genomics
Laboratory is part of Genomics Research (http://www.mtt.fi/english/research/biotechnology/genomics.html),
which includes plants, animals, and microbes, within the Department of Biotechnology
and Food Research (http://www.mtt.fi/english/research/biotechnology/biotechnology.html).
Genomics Research is directed by Prof. Alan H. Schulman.

The Plant Genomics unit is based in two laboratories, one at
Jokioinen and a joint laboratory with the Institute of Biotechnology of the University
of Helsinki, which is located in the Viikki Biocenter (http://www.biocenter.helsinki.fi/bi/bare-1_html/bare1.htm).
The University of Helsinki (www.helsinki.fi) has the
widest range of disciplines in Finland. It was established in Turku in 1640,
but was transferred to Helsinki in 1828. The number of faculties is eleven.
There are 38,000 degree students and 7,600 staff.
The number of degrees taken each year is almost 4,300, of which 400 are doctorates.
The Institute of Biotechnology (http://www.biocenter.helsinki.fi/bi/)
at the University of Helsinki is an administratively
independent unit for promoting research and education in biotechnology,
molecular biology, cell biology, and related areas. The Institute was founded
in 1989. Its mission is to promote high-level research and graduate training
and to integrate the interests of several faculties within the
University of Helsinki by serving as a bridge between them in research,
technology
transfer and post-graduate education.

Picture: During 2006, more than 200 GM barley lines have been produced with a transformation efficiency ~10%.
The Plant Genomics Group carries out research on
retrotransposons as drivers of genomic change and as markers for this change,
uses these and other marker systems for map-based cloning of genes for disease
resistance and quality traits, and analyses the role of candidate genes through
the application of functional genomics tools such as microarrays. To support
these goals, we develop and apply doubled-haploid populations for mapping
purposes in barley, rye, oat, and Brassica. Genome organisation and the
role of retrotransposons is currently under study in the emerging model species
Brachypodium distachyon. This plant is closer to the Triticeae including
barley and wheat than is rice, and should prove very helpful as a scaffold for
gene isolation in the important Nordic cereals and grasses. We also have
implemented barley transformation using Agrobacterium. Potato
di-haploids and fusions have been produced and are being used to engineer
disease resistance.
The group has a long-term programme to understand the role
of retrotransposons in genome dynamics. These mobile elements replicate in a
way similar to retroviruses and create daughter copies that integrate
throughout the genome. They may also be removed by intrachromosomal
recombination. We are interested in establishing the details of their
lifecycle, the role of cellular components in controlling their capacity for
enormous copy number increase and mutagenic genome disruption, and their effect
on genomic and cellular function.

Picture: Retrotransposon virus-like particles isolated by sucrose gradient from barley
The group also develops and applies retrotransposons as
molecular markers for fingerprinting, biodiversity, and breeding applications.
Barley is the main plant for basic research, but to date we have developed and
applied marker systems for barley, wheat, oat, timothy grass, potato, banana,
and oil palm. We also develop and apply microsatellite and SNP-based markers
such as can be derived from ESTs. We also carry out pathogen-side research on
the net blotch disease of barley, examing virulence in the fungus Pyrenophora
teres teres.
We are applying the Affymetrix barley microarray platform to
analyse grain development and germination as well as biotic (fungal resistance)
and abiotic (drought) response and resistance. Earlier, we sequenced 44 000
barley ESTs from 18 libaries, established both the wet-lab and bioinformatics
pipeline to do so, and contributed these to the worldwide, American-based
efforts that led to the production of the Affymetrix chip. The group has about
30 members currently.
We are well equipped for our activities. Facilities in
Helsinki include ABI 377, ABI 3100, and ABI 377 sequencers, ScanArray 5000
microarray reader, Qiagen Biorobots 3000 for rearraying ESTs, Qiagen Biorobot
8000 for high-throughput PCR purifications for arrays, Qiagen Biorobot 9600,
Tecan Genesis RSP 100, Tecan Genesis 500 for setting up reactions and preparing
bacterial stocks, three plate-filling robots, a Genetix Q-PIX for picking
colonies, three MJ Research tetrads and five ABI GeneAmp 9700s for EST PCRs for
arrays, a Qiagen/Retch 96-well high-throughput DNA prep system, and standard
molecular biological equipment including an ultracentrifuge and superspeed
centrifuges, growth chambers, flow benches, and electrophoresis boxes. We are
currently awaiting during 2006 the installation of a 454 Life Sciences (Roche) GS20
massively parallel sequencer. The Jokioinen lab, in addition to molecular
biology facilities, has excellent glasshouse, farm-scale and phenotyping
facilities. The bioinformatics group has powerful unix workstations and a new
ten-processor cluster at their disposal, as well as the requisite databases,
programming tools, and applications both written locally and obtained as
packages.

Picture: Barley varieties genotyped with IRAP markers based on LARD retrotransposons
- Tanskanen, J.A., Sabot, F. Vicient, C. &
Schulman, A.H. 2006. Life without GAG: The BARE-2
retrotransposon as a parasite’s parasite. Gene, in press 7.09.06
- Druka, A., Muehlbauer, G., Druka, I., Caldo, R.,
Baumann, U., Rostoks, R., Schreiber, A., Wise, R., Close, T., Kleinhofs, A.,
Graner, A., Schulman, A., Langridge, P., Sato, K., Hayes, P., McNicol, J.,
Marshall, D. & Waugh, R. 2006. An atlas of gene expression from seed to
seed through barley development. Funct. Integr. Genomics DOI: 10.1007/s10142‑006‑0025‑4
- Tanhuanpää, P., Kalendar, R., Laurila, J., Schulman,
A.H., Manninen, O. & Kiviharju, E. 2006. Generation of SNP markers for
short straw in oat (Avena sativa L.). Genome 49 (3): 282-287.
- Kalendar, R., Vicient, C.M., Peleg, O.,
Anamthawat-Jonsson, K., Bolshoy, A. and Schulman, A.H. 2004. LARD
retroelements: Novel, non-autonomous components of barley and related genomes.
Genetics 166(3): 1437-1450.
- Leigh, F., Kalendar, R., Lea, V., Lee, D. Donini, P. &
Schulman , A. H. 2003. Comparison of the utility of barley
retrotransposon families for genetic analysis by molecular marker techniques.
Mol. Genet. Genomics 269: 464-474.
- Tanhuanpää, P. & Schulman, A.H. 2002. Mapping genes affecting linolenic acid content in Brassica
RAPA ssp. Mol. Breeding.10: 51-62.
- Boyko, E., Kalendar, R., Korzun, V. Korol, A.,
Schulman, A.H., Bikram, G. 2002. Aegilops tauschii
high density genetic map of expressed and repeated fractions of the genome
provides unique insights into cereal chromosome structure and function. Plant
Mol. Biol. 48: 767 - 790. Cover photo.
- Vicient, C.M., Kalendar, R. and Schulman, A.H.
2001. Envelope-class retrovirus-like elements are widespread, transcribed and
spliced, and insertionally polymorphic in plants. Genome Res. 11: 2041-2049.
- Shirasu, K., Schulman, A.H., Lahaye, T. &
Schulze-Lefert, P. 2000. A contiguous 66 kb barley
DNA sequence provides evidence for reversible genome expansion. Genome Res.
10: 908-915
- Kalendar, R., Tanskanen, J., Immonen, S., Nevo, E. & Schulman,
A.H. 2000. Genome evolution of wild barley (Hordeum
spontaneum) by BARE-1 retrotransposon dynamics in response to sharp
microclimatic divergence. Proc. Natl. Acad. Sci. USA 97(12): 6603-6607.
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