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What's Newsworthy......
archives of previous postings
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content to this feature
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03-Oct-03
Message from Publisher: This message is to announce
that our staff will be taking a sabbatical from updating this
What's Newsworthy Feature of our web site until further
notice. The staff are needed to work on another important
project and we have not yet identified a volunteer editor who
will step in and provide new content for this feature bimonthly
(it's okay for faculty to volunteer their students and post-docs
so they can practice their writing skills and ensure they keep
up on their journal reading). The good news is that we will,
however, continue to update the What's being patented and What's
being published features as before. We have enjoyed
providing this feature and look forward to providing it again as
soon as possible.
Sincerely,
Fred Lehle, Ph.D.
Chief Editor and Publisher |
Glycerolipid biosynthesis
outside the plastidic compartments concerns membrane as well as storage
lipid metabolism. The initial step is mediated by the membrane-bound
enzyme, GPAT1 (glycerol-3-phosphate acyltransferase 1). The GPAT1
gene family from Arabidopsis has been recently characterized by J
Zou and associates at the National
Research Council of Canada, Saskatoon.
In the August 03 issue of Plant
Cell (vol 15: 1872-87), the above authors report the effect of the AtGPAT1
gene family on
tapetum differentiation and pollen development. In order to study the
role of this gene in gametophytic development, the authors expressed
polypeptides encoded by this gene in a yeast lipid mutant and also
disrupted one isoform of this gene. They observed that disruption of the
GPAT1 gene adversely affected pollen development. Male
fertility was restored upon introduction of the normal allele of this
gene into the mutant. Restoration of pollen development by substitution
of the mutant allele with its normal counterpart, confirmed that there
is a strong correlation between GPAT1 and pollen development.
From their microscopic studies, the authors concluded that the
disrupted GPAT1 gene causes degeneration of the tapetum and
structural modification of the endoplasmic reticulum, accompanied by
reduced secretion. The authors also found that in the absence of an GPAT1
gene, pollination fails, signifying its importance on pollen
performance. The composition of fatty acids changed considerably in the
floral tissues and seeds. Interestingly, these changes were not
reflected in seed oil content in a significant manner.
Click here
for details.
The mechanisms underlying the
organization of cell layers in the development of plant organs are not
fully understood. In order to gain insight into the progression of
events that lead to differentiation of peripheral cell layers, GC Ingram
and associates at the ICMB,
the University of Edinburgh, cloned the ARABIDOPSIS CRINKLY4 gene and
studied its expression in fast dividing cells in various meristematic
zones.
In the September, 03 issue of Development
(vol 130:4249-58), the above authors report that they have
characterized the ARABIDOPSIS CRINKLY4 gene. Their study reveals
that this gene encodes a functional kinase and that it is expressed in the
L1 cell layer of most of the meristematic and organ primordial tissues
such as the ovule integuments. Using insertional mutations, they were
able to show that this gene regulates cellular organization of certain
organ development such as sepal margins and the integument around the
nucellar tissue. The abundant presence of the receptor kinase in
anticlinal and the inner periclinal plasma membrane of 'exterior' cells
indicates that the above gene plays a significant role in certain
developmental process restricted to outer meristematic cell layers.
Based on their findings, the authors propose that ARABIDOPSIS
CRINKLY4 organizes and maintains external cell layers in organs of
vital importance by receiving and transmitting signals from adjoining L1
cell layers alone or possibly both from L1- and underlying layers of
cells.
Click here
for details.
It is known for quite some time that calcium plays a significant role
in signal transduction pathways. Calcium critically influences the
expression of stress-related genes. However, the molecular mechanism
underlying calcium function has not yet been worked out. It is
believed that in the cytosol there are sensor molecules such as calcium
binding proteins that recognize calcium changes within the cell. It is
also known that there are calcineurin B-like (CBL)
protein families that act as calcium sensors in plants.
In the August, 03 issue of Plant Cell (vol.15:1833-45), a team
of scientists led by S.
Luan at the Department of Plant and Microbial Biology, UCB, report
that CBL1, a member of the CBL family CBL1, is highly stress
sensitive and is induced by multiple stress signals. An increase in the CBL1-encoded
protein level in transgenic Arabidopsis plants was found to
modify the stress response pathways in these plants. The authors studies
further revealed that this gene acted differently under different kinds of stress. For
example, CBL1 positively
regulates the drought-induced gene expression but negatively regulate
the cold-responsive genes. Consistent with this, transgenics
over-expressing CBL1 became more tolerant to salt and drought,
while their susceptibility to freezing temperatures increased.
Conversely, the cold tolerance capacity of cbl1 null mutants in Arabidopsis
plants increased, while these mutants were more susceptible in the
drought and saline environment. The authors concluded that depending
upon the environment, CBL1 acts as a positive or a negative
regulator of stress responses.
Click here
for details.
|

Dr.
John P. Helgeson
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08-Aug-03
Gene RB Cloned from Solanum
Bulbocastanum Confers Broad Spectrum Resistance to Potato Late
Blight |
Phytophthora infestans
causes late blight disease of potato. In certain years the damage is
very severe. Fungicide treatment has thus far been the only solution to
contain this ravaging disease in the USA and other developed countries.
No potato cultivars in the USA are known to contain genes that confer
resistance to late blight. The absence of a resistant potato variety
prompted a research team led by J. Jiang and J.P.
Helgeson at the University of Wisconsin, Madison (WUM) to survey a
wide range of Solanum species, searching for genes that would protect
the potato crop against this deadly disease. When laboratory tests
revealed that S. bulbocastanum, a wild diploid potato species is
highly resistant to all known races of P. infestans, they cloned
the gene and designated it the RB gene. The effective and long-lasting
resistance ability of this diploid species was also demonstrated in the
field.
In the July 18, 2003, online publication of PNAS, the
12-member team affiliated to USDA, UCD, UWM and two other institutions,
report the cloning of the major resistance gene RB in S.
bulbocastanum. The authors used a combination of techniques: a map-based
method supported by a long-range (LR)-PCR strategy. Their study revealed
a cluster of four resistance genes of the CC-NBS-LRR (coiled
coil-nucleotide binding site-Leu-rich repeat) class. They were located
within the genetically mapped RB region. Transgenics transformed with
one of these four genes showed late blight resistance over a wide range
of pathogen races. Thus, the above investigation yielded the cloned RB
gene - a new resistance source for developing late blight resistant
potato varieties. Another byproduct of this investigation has been the
demonstration that LR-PCR method can be used to isolate genes that
cannot be maintained in the bacterial artificial chromosome system.
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arabidopsis.com
STAFF |
Publisher
& Editor
Fredric R. Lehle
Art & Production
Naomi Hamel
respice, adspice, prospice
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| Sales
Manager Messages
archives |
| 08
May 2007 Custom Project Price Guide - Fall 2007
Pricing for custom project services for the
Fall 2007 production cycle are shown in the following table.
|
Destination of Project Products |
|
USA |
Foreign |
| Genome Classification |
|
Service
|
Non-
Transgenic |
Transgenic |
Non-
Transgenic |
Transgenic |
| Custom EMS mutation for M1 seeds¶ |
$2,090 |
$2,290 |
$2,090 |
$2,590 |
|
| Custom EMS mutation for M2 seeds¥ |
$2,140 |
$2,340 |
$2,140 |
$2,640 |
| Custom M1 grow-out & selfing to M2, 12 flats
(minimum)§ |
$2,900 |
$3,200 |
$2,900 |
$3,200 |
| Total |
$5,040 |
$5,540 |
$5,040 |
$5,840 |
| ¶
Fee covers mutation and M1 seed
drying services. A maximum of 1.5 grams of seeds are
mutated per batch and then dried and shipped. Includes
chemical waste neutralization, treatment and disposal
services. Where applicable, includes extra fees
associated with transgenic biologicals such as their 1) special
handling, containment and disposal and 2) compliance with USDA APHIS
regulations to obtain a project specific importation permit.
Shipping and any related costs are not included. A $500
retainer is required to engage this service. Billing is monthly
thereafter.
¥ Fee
covers mutation and M1 seed stratification services. A maximum
of 1.5 grams of seeds are mutated per batch and stratified at 5 C in
preparation of planting. Fees for actual planting and grow-out
of M1 seeds are covered in following service. Includes
chemical waste neutralization, treatment and disposal
services. Where applicable, includes
extra fees associated with transgenic biologicals such as their 1)
special handling, containment and disposal and 2) compliance with
any or all USDA APHIS regulations to obtain a project specific
importation permit. Shipping and any related costs are not
included. A $500 retainer is required to engage this service.
Billing is monthly thereafter.
§ Fee
covers M1 seed sowing, growing, maintaining, selfing, harvesting,
cleaning and packaging of M2 progeny seeds for 4-5 months.
This service is paired with and follows the Custom EMS mutation
service for M2 (above). M1
seed are planted to achieve a target stand of 1,100 M1 parents
on each of a minimum of twelve 28 x 56 cm greenhouse flats.
Sowing rate is 0.06 grams per flat. Add $242 or $267 for each
additional flat for non-transgenic and transgenic seeds,
respectively. Fee includes a stand count, embryo test for
mutation frequency estimation and remote monitoring of project via
images posted to our web site. Where applicable, includes extra fees associated
with rendering harmless and disposing of transgenic biologicals or
medium containing their residues. Shipping
and any related costs are not included. Billing is
monthly. |
19
Feb 2007 Effective today, prices of ARASYSTEM components
will be increased across the product line an average of 2.3% to reflect
recent devaluation
in the dollar.
|
| Production
Manager Messages
archives |
| 19 Apr
2007 Notice of Custom Project Schedule
The schedule for custom projects for the
remainder of 2007 and the first half of 2008 have been finalized.
Custom projects requiring a grow-out of M2 seeds must be initiated either
in the months of September 2007 or February 2008. This scheduling is
required so custom projects coincide with our regular growth room
operations. LEHLE SEEDS currently idles its growth rooms from June
to August for insect control, equipment maintenance, cleaning and
disinfection. The time is also used for processing chemical waste
and growth medium waste prior to disposal. Important deadlines are
summarized in the following two sections.
Fall 2007
Custom Projects - Reservations now being accepted
15 Jul 2007 -
Last day to submit application for importation permit for September 2007
custom projects where client is 1) outside the U.S.A. and seeds are 2)
transgenic.
01 Sep 2007 -
Last day to receive seeds for September 2007 custom projects. Seeds
received after this date will be scheduled for February 2008.
01 Sep 2007 - 30 Sep
2007 Dates when custom projects with M2 grow-out will be initiated. Projects
not initiated by 30 Sep 2007 will be scheduled for February 2008.
31 Jan 2008 (or
earlier) - Fall 2007 custom project harvesting complete.
Spring 2008
Custom Projects - Reservations now being accepted
15 Dec 2007 -
Last day to submit application for importation permit for February 2008
custom projects where client is 1) outside the U.S.A. and seeds are 2)
transgenic.
01 Feb 2008 -
Last day to receive seeds for September 2007 custom projects. Seeds
received after this date will be scheduled for September 2008.
01 Feb 2008 - 29 Feb
2008 Dates when custom projects with M2 grow-out will be initiated. Projects
not initiated by 29 Feb 2008 will be scheduled for Sep 2008.
30 Jun 2008 (or
earlier) - Spring 2008 custom project harvesting complete.
Additional information concerning custom projects
Space in our growing rooms is limited and
projects are assigned to the available space on a first come, first serve
basis. Projects that involve the importation of transgenic seeds
into the U.S. will require LEHLE SEEDS to obtain a special USDA APHIS
importation permit. The permit process is such that the application
should be started in July 2007 for the September custom projects and in
December 2007 for the February 2008 custom projects. For
September 2007 projects, seeds must be in our hands no later than
September 1, 2007. For February 2008 projects, seeds must be in our
hands no later than February 1, 2008. Transgenic as well as
non-transgenic seeds can be submitted, but transgenic seeds can only be
imported to the USA under a special USDA APHIS which LEHLE SEEDS will
obtain for its foreign customers before importation. Contact Fred
Lehle, Ph.D. by email if you have additional questions or
interest.
Custom projects involving no M1 grow-out
Custom projects with immediate return of
air-dried M1 seeds will be conducted only during the months of September -
October 2007 and February - March 2008.
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