3 my $page=CXGN
::Page
->new('200510','Teri Solow');
5 my $stylesheet=<<END_STYLESHEET;
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10 background-color: #ffffff;
31 $page->header('The Jahn Lab', undef, $stylesheet);
38 <p
class="footnote"><img src
="/static_content/community/feature/200510-1.jpg" border
="4" style
="border-color: #000000" width
="800" height
="600" alt
="Jahn Lab" /><br
/>
41 <p style
="border-bottom: 0px">The research
in our group focuses on gene discovery
, the analysis of
42 genome structure
and function
and the relevance of this information
for the
43 improvement of useful plants
. Work
in our program includes fundamental
44 studies of the relationship between model species
and less well
-
45 characterized crop species
, the release of varieties
and advanced breeding
46 lines
, development of improved selection strategies
, and research on the
47 genetics of disease resistance
and fruit quality
. Specifically
, a major
48 effort
in the lab is to demonstrate the extent to which results from a
49 leading plant model
, tomato
, are relevant to the related
, but much less
50 well
-characterized genus
, <em
>Capsicum
</em
>, the garden pepper
. Towards this end we
51 have developed a detailed comparative genetic
map for the Solanaceae now
52 defining the broadest comparative genetic
system in the dicots
. We have
53 used this tool to identify candidates
for traits with simple
and
54 quantitative inheritance
and to assess the relationships between genes
in
55 tomato
and pepper that affect similar
or related traits
. Further studies
56 are focusing on traits considered distinctive
</p
>
58 <p
class="footnote" style
="float:right; width:375px; text-align:center;"><img src
="/static_content/community/feature/200510-2.gif" border
="4" style
="border-color: darkgreen" width
="333" height
="229" alt
="Different species and varieties of pepper" /><br
/>
59 Different species
and varieties of pepper
for a genus
, e
.g
., pungency
.
62 <p style
="border-top:0px">Finally
, the Solanaceae have afforded a unique
63 glimpse of the organization of resistance genes
in plant genomes
. We have
64 shown that despite co
-evolutionary forces
in host
/pathogen interactions
,
65 disease resistance genes represent ancient lineages
in plants
and that
66 resistance pathways may be very highly conserved
. We also have extensive
67 gene discovery
and breeding activities that integrate classical
and
68 molecular methods
for generating
and selecting desirable genetic
69 variability
, primarily focused on the identification of new sources of
70 biotic
and abiotic stress resistance from wild accessions
and related
71 species
in cucurbits
, <em
>Phaseolus
</em
> and pepper
. The Public Seed Initiative is
72 an outreach activity based on an alliance of public sector researchers
and
73 non
-profit groups interested
in improving the dissemination
and utilization
74 of public plant varieties
and crop genetic diversity
.</p
>
76 <p
>Pungency
in pepper pods is a consequence of accumulation of the alkaloid
77 capsaicin
(shown below
) and its analogs
. The biosynthesis of capsaicin is
78 restricted to the genus
<em
>Capsicum
</em
> and results from the acylation of an
79 aromatic moiety
, vanillylamine
, by a branched chain fatty acid
. Apart from
80 portions of the biosynthetic pathway common to other primary metabolic
81 pathways
, the remainder of the pathway remains unknown
. One of the major
82 projects within
our group focuses on capsaicin biosynthesis
and the genes
83 that define
and regulate the pathway
.</p
>
85 <p
class="footnote" style
="float:right; width:440px; text-align:center;"><img src
="/static_content/community/feature/200510-3.gif" border
="0" width
="398" height
="103" alt
="Molecular structure of capsaicin" /><br
/>
86 Molecular structure of capsaicin
89 <p
>Due to the popularity
and familiarity of products containing capsaicin
90 there is rapidly growing economic significance
in a wide array of food
91 products
, in medicine
, industry
, law enforcement
, and pest control
(it has
92 become a leading insect protectant
in organic agriculture
and is the active
93 ingredient
in many of the most effective deer
and rodent repellents
). Considering the importance of this pathway
, it
94 is surprising that relatively little is known
, particularly at the
95 molecular level
, concerning the molecular genetics
, biosynthesis
,
96 subcellular localization
and cellular structures required
for pungency
97 accumulation
in peppers
. The recent cloning
and initial characterization of
98 <em
>Pun
1</em> (formerly known as <em>C</em
>) allows
for new insight into capsaicin
99 biosynthesis
and accumulation
. <em
>pun
1</em
> was first reported nearly
100 years
100 ago
and was shown to be epistatic to all other pungency
-related genes
101 (Webber
, 1911). At present
, the
<em
>pun1
</em
> allele is the only confirmed mutation
102 that has a qualitative affect on the presence
/absence of capsaicinoids
103 (Blum et al
., 2002 and references therein
). Further characterization of
104 <em
>Pun
1</em
>, as well as other candidates implicated
in pungency is currently
107 <p
>Another area of research
in our lab is potyvirus resistance
. Mutations
108 in the eIF4E homolog
, encoded at the
<em
>pvr1
</em
> locus
, result
in broad
-spectrum
109 potyvirus resistance conferred by
<em
>pvr1
</em
> resistance allele
in Capsicum
, a
110 gene widely deployed
in agriculture
. Point mutations
in recessive
111 resistance genes
, <em
>pvr1
</em>, <em>pvr1<sup>1</sup></em> and <em>pvr1<sup>2</sup></em
>, grouped to similar regions of the
112 <em
>eIF4E
</em
> gene
and were predicted by protein homology models to cause
113 conformational shifts
in the encoded proteins
. While the protein encoded by
114 <em
>pvr1
<sup
>+</sup></em
> interacts strongly
, proteins translated from all three resistance
115 alleles
(<em
>pvr1
</em>, <em>pvr1<sup>1</sup></em> and <em>pvr1<sup>2</sup></em
>) failed to
bind VPg from either strain of
116 TEV
in a yeast two hybrid assay
. This failure to
bind correlates with
117 resistance
, suggesting that interruption of the interaction between VPg
and
118 this eIF4E paralog may be necessary
, but is
not sufficient
for potyvirus
119 resistance
<em
>in vivo
</em>. Among the three resistance alleles, only the <em>pvr1</em
>
120 gene product fails to
bind m
<sup
>7</sup
>-GTP cap
-analog columns
, suggesting that
121 disrupted cap
-binding is
not required
for potyvirus resistance
.</p
>
123 <p
class="footnote" style
="float:left; width:350px; text-align:center;">
124 <img src
="/static_content/community/feature/200510-5.gif" border
="4" style
="border-color: #000000" width
="281" height
="215" alt
="Pepper infected with Tobacco Etch Virus" />
126 Uninfected pepper plant
129 <p
class="footnote" style
="float:right; width:350px; text-align:center;">
130 <img src
="/static_content/community/feature/200510-4.gif" border
="4" style
="border-color: #000000" width
="280" height
="215" alt
="Uninfected pepper plant" />
132 Pepper infected with Tobacco Etch Virus
137 <div style
="float:left; width:250; text-align:left;">
138 <h2
>Contact Information
</h2
>
142 313 Bradfield Hall
<br
/>
143 Plant Breeding
and Genetics
<br
/>
144 Cornell University
<br
/>
145 Ithaca
, NY
14853<br
/>
146 <a href
="mailto:mmj9\@cornell.edu">mmj9\
@cornell.edu
</a><br />
148 607.255.6683 (fax
)<br
/>
152 <p
class="footnote" style
="float:right; width:400px; text-align:center;"><img src
="/static_content/community/feature/200510-6.gif" border
="0" width
="179" height
="164" alt
="Swirly image" /><br
/>
153 </p><br clear="all" />
155 <h2
>Selected Publications
</h2
>
157 <p
class="bibliography">
158 Kang
, B
.-C
., I
.H
. Yeam
, J
.D
. Frantz
, and M
.M
. Jahn
. 2005. Mutations
in
159 translation initiation factor eIF4E that confer resistance to potyvirus
160 infection abolish interaction with Tobacco etch virus VPg
in a non
-
161 specific manner
. Plant J
. 42:392-405.
164 <p
class="bibliography">
165 Stewart
, C
. Jr
., B
.-C
. Kang
, K
. Liu
, M
. Mazourek
, S
. Moore
, M
.M
. and Jahn
.
166 2005. The Pun1 gene
for pungency
in pepper encodes a putative
167 acyltransferase
. Plant J
. 42:675-688.
170 <p
class="bibliography">
171 Liu
, K
., B
.-C
. Kang
, H
. Jiang
, C
.B
. Watkins
, T
.L
. Setter
and M
.M
. Jahn
.
172 2005. Identification
and characterization of an auxin
-responsive GH3
-
173 like gene
in pepper fruit development
. (accepted Plant Mol
. Biol
.).
176 <p
class="bibliography">
177 E
. A
. Quirin
, E
. Ogundiwin
, J
.P
. Prince
, M
. Mazourek
, M
. O
. Briggs
, T
. S
.
178 Chlanda
, K
.T
. Kim
, M
. Falise
, B
.-C
. Kang
, and M
.M
. Jahn
. 2005.
179 Development of sequence characterized amplified region
(SCAR
) primers
180 for the detection of Phyto
.5.2, a major QTL
for resistance to
181 Phtophthora capsici Leon
. in pepper
.Theor
. Appl
. Genet
. 110(4):605-12.
184 <p
class="bibliography">
185 Kang
, B
.-C
., and I
. H
. Yeam
, and M
.M
. Jahn
. 2005. Virus resistance genes
.
186 Ann
. Rev
. of Phytopath
. E
. pub
. May
2. 43:581-621.
189 <p
class="bibliography">
190 Porch
, T
.G
., M
.H
. Dickson
, M
. Long
, D
.R
. Viands
, and M
.M
. Jahn
. 2005.
191 General combining ability effects
for reproductive heat tolerance
in
192 snap bean
. J
. Agriculture U
. Puerto Rico
88(3-4):x
-x
.
195 <p
class="bibliography">
196 Qian C
.T
., M
.M
. Jahn
, J
.E
. Staub
, X
.-D
. Luo
and J
.F
. Chen
. 2005. Meiotic
198 behavior
in an allotriploid derived from an amphidiploid x diploid
199 mating
in Cucumis
. accepted Plant Breeding
202 <p
class="bibliography">
203 Henning
, M
.J
, H
.M
. Munger
and M
.M
. Jahn
. 2005. 'Hannah's Choice F1
' : A
204 new muskmelon hybrid with resistance to powdery mildew, Fusarium race 2
205 and potyviruses. HortScience in press.
208 <p class="bibliography">
209 Henning, M.J, H.M. Munger and M.M. Jahn. 2005. 'PMR Delicious
51': An
210 improved open-pollinated melon with resistance to powdery mildew.
211 HortScience 40(1):261-262.
214 <p class="bibliography">
215 Paran, I., J. Rouppe van der Voort, V. Lefebvre, M.M. Jahn, L. Landry, R.
216 van Wijk, H. Verbakel, B. Tanyolac, C. Caranta, A. Ben Chaim, K.D.
217 Livingstone, A. Palloix and J. Peleman. 2004. An integrated genetic
218 map of pepper. Molecular Breeding 13:251-261.
221 <p class="bibliography">
222 Chen, J., X. Luo, C. Qian, M.M. Jahn, J.E. Staub, F. Zhuang, Q. Lou and G.
223 Ren. 2004. Cucumis monosomic alien addition lines: morphological,
224 cytological and RAPD analysis. TAG 108:1343-1348.
227 <p class="bibliography">
228 Alba, R., Z. Fei, P. Payton, Y. Liu, S.L. Moore, P. Debbie, J.S. Gordon,
229 J.K.C. Rose, G. Martin, S.D. Tanksley, M. Bouzayen, M.M. Jahn and J.
230 Giovannoni. 2004. ESTs, cDNA microarrays and gene expression
231 profiling: tools for dissecting plant physiology and development.
235 <p class="bibliography">
236 Rose, J.K.C., S. Bashir, JJ Giovannoni, MM Jahn and R.S. Saravanan. 2004.
237 Tackling the plant proteome: practical approaches, hurdles and
238 experimental tools. Plant J 39:715-733.
241 <p class="bibliography">
242 Nelson, R.J., R. Naylor and M.M. Jahn. 2004. The role of genomics research
243 in the improvement of orphan crops. Crop Science 44:1901-1904.