1 KK3, all located within 20 kb of the mekk1-1
T-DNA insertion.
2 hich the At2g37940 locus is knocked out by a
T-DNA insertion.
3 ted a mutant in which NPG1 is disrupted by a
T-DNA insertion.
4 ecessive mutation that cosegregated with the
T-DNA insertion.
5 ncoding this enzyme (DPE1) is disrupted by a
T-DNA insertion.
6 using either artificial microRNAs or a LOG2
T-DNA insertion.
7 nsertion site densities in exons than do the
T-DNA insertions.
8 s mediated by trans-interactions between two
T-DNA insertions.
9 as9 system can efficiently generate targeted
T-DNA insertions.
10 ndent phyA alleles, ars4, phyA-211 and a new
T-DNA insertion allele (phyA-t) show increased tolerance
11 Characterization of an independent paf1
T-DNA insertion allele and complementation by PAF1 confi
12 A
T-DNA insertion allele in DRP1E did not cause powdery mi
13 A
T-DNA insertion allele of SHM1, shm1-2, and the F1 proge
14 We have identified a
T-DNA insertion allele of the ATEM6 gene in which the T-
15 SUSCEPTIBLE1) gene of Arabidopsis based on a
T-DNA insertion allele that resulted in increased suscep
16 A strong
T-DNA insertion allele, ftsHi1-2, caused embryo-lethalit
17 More severe scd1
T-DNA insertion alleles (scd1-2 and scd1-3) markedly aff
18 e to A. brassicicola and B. cinerea, whereas
T-DNA insertion alleles are embryonic lethal, suggesting
19 We identified
T-DNA insertion alleles disrupted in five of the nine co
20 lations segregating for the cki1-5 or cki1-6
T-DNA insertion alleles failed to reveal any homozygous
21 The characterization of two Arabidopsis
T-DNA insertion alleles for AESP demonstrated that it is
22 In addition, two independent
T-DNA insertion alleles in the WRKY70 gene showed increa
23 light and plastid signals by characterizing
T-DNA insertion alleles of genes that are regulated by l
24 d Arabidopsis GTG1 and GTG2 and isolated new
T-DNA insertion alleles of GTG1 and GTG2 in both Wassile
25 T-DNA insertion alleles of ZFAR1 (At2G40140), the gene e
26 siz1-2 and siz1-3
T-DNA insertion alleles that caused freezing and chillin
27 yses of multiple itb2 alleles, including the
T-DNA insertion alleles, showed that the loss of ITB2/AL
28 The
T-DNA insertion and RNAi mutant plants displayed enhance
29 we have characterized both loss-of-function
T-DNA insertion and RNAi mutants and gain-of-function tr
30 id occur in plants homozygous for the dcl3-1
T-DNA insertion and was unaffected by loss of function o
31 The
T-DNA insertion appeared in the first exon of an open re
32 The other three
T-DNA insertions are associated with a partial transmiss
33 ecting and characterizing lines in which the
T-DNA insertions are present specifically within introns
34 The ars4ars5 double mutant contains a single
T-DNA insertion,
ars4, which co-segregates with arsenic
35 A transgenic line with a
T-DNA insertion at 40-bp upstream of the WAKL4 start cod
36 Analysis of this mutant revealed a
T-DNA insertion at the first exon of an Arabidopsis thal
37 Here, we isolated two mutants that carry
T-DNA insertions at the At1g31870 locus and shows early
38 125 lines (genetically, each contains single
T-DNA insertion)
by six senescence-promoting factors, na
39 In the mutant, the
T-DNA insertion caused a 40 % rise in transcript levels
40 el mutant screen, combining a confirmed SALK
T-DNA insertion collection with traditional forward gene
41 of the DUF579 family have been disrupted by
T-DNA insertions contain less xylose in the secondary ce
42 the ABA insensitivity was linked to a single
T-DNA insertion containing a 35ScDNA fusion.
43 nuclear gene PIFI (At3g15840) containing the
T-DNA insertion encodes a chloroplast-targeted protein l
44 In an effort to detect targeted
T-DNA insertion events, we built another T-DNA with a pr
45 0 independent Agrobacterium transferred DNA (
T-DNA) insertion events in the genome of the reference p
46 00 insertion lines (including transposon and
T-DNA insertions)
from several tagging programs in Arabi
47 ds in which both PMDH genes are disrupted by
T-DNA insertions germinate, but seedling establishment i
48 While the
T-DNA insertion had little effect on the WAKL4 transcrip
49 Tight linkage of Def-1 to a
T-DNA insertion harboring the maize (Zea mays) Dissociat
50 re the respective gene has been disrupted by
T-DNA insertion have been characterized.
51 Seedlings homozygous for the
T-DNA insertion have no obvious mutant phenotype.
52 Arabidopsis thaliana lines containing mapped
T-DNA insertions have become an important resource for p
53 fem111 contains a
T-DNA insertion in AGAMOUS-LIKE80 (AGL80).
54 The ahp2-1 mutation was caused by a
T-DNA insertion in an Arabidopsis homologue of meu13+, w
55 A
T-DNA insertion in Arabidopsis thaliana pdTPI resulted i
56 Arabidopsis carrying a
T-DNA insertion in At3g15870 had wild-type levels of bot
57 An Arabidopsis mutant with a
T-DNA insertion in At4g14070 (AAE15) was reduced 80% in
58 regulated in A. thaliana plants containing a
T-DNA insertion in AtHD1 (athd1-t1), indicating that AtH
59 Loss-of-function mutation by
T-DNA insertion in AtPAT21 results in the complete failu
60 dopsis thaliana) pex5-10 mutant, which has a
T-DNA insertion in exon 5 of the PEX5 gene.
61 Flowers of a mutant line carrying a
T-DNA insertion in gene At5g44630 emitted these three se
62 Plants harboring a
T-DNA insertion in KU70 exhibit no growth or development
63 ut homozygous Arabidopsis mutant line with a
T-DNA insertion in LIP5.
64 Using a
T-DNA insertion in one AP2 transcription factor (redox-r
65 distachyon, we identified a line carrying a
T-DNA insertion in one of the two eukaryotic initiation
66 nfd1 contains a
T-DNA insertion in RPL21M that is predicted to encode th
67 cond AtOPT3 mutant line, opt3-2, harboring a
T-DNA insertion in the 5' untranslated region of AtOPT3.
68 d two independent Arabidopsis mutants with a
T-DNA insertion in the AtBI1 gene.
69 an Arabidopsis mutant (atfut1) containing a
T-DNA insertion in the AtFUT1 locus and transgenic plant
70 The
T-DNA insertion in the AtOPT3 promoter resulted in reduc
71 We characterized a mutant (Delta8L4) with a
T-DNA insertion in the coding sequence of the gene At4g2
72 , we identified an Arabidopsis mutant with a
T-DNA insertion in the FATB gene.
73 plants unable to metabolize maltose due to a
T-DNA insertion in the gene for the cytosolic amylomalta
74 le-related defects in the iar4 mutant, and a
T-DNA insertion in the IAR4 coding sequence conferred si
75 We next analyzed a
T-DNA insertion in the MEKK2 promoter region and found t
76 Southern blot analyses indicated a single
T-DNA insertion in the mutant, located on chromosome 10.
77 sis of the arp4-1 mutant allele, which has a
T-DNA insertion in the promoter region and a moderate re
78 A
T-DNA insertion in the promoter region downstream of two
79 racterization of a mutant that contained the
T-DNA insertion in the promoter region of the TK1a gene.
80 These phenotypes are a result of a
T-DNA insertion in the SQUAMOSA promoter binding protein
81 This mutant, sqd2 pgp1-1, carries a
T-DNA insertion in the structural gene for SQDG synthase
82 s of Sultr1;2, while the sel1-9 mutant has a
T-DNA insertion in the Sultr1;2 promoter.
83 ith impaired pollen development and a single
T-DNA insertion in the transcription factor gene bHLH142
84 We have further identified a
T-DNA insertion in the UVH6/AtXPD gene (uvh6-2).
85 A
T-DNA insertion in the XXT5 gene generates a readily vis
86 We identified a
T-DNA insertion in this gene which abolishes its express
87 Seeds homozygous for
T-DNA insertions in AESP exhibited embryo arrest at the
88 have allowed the search for plants carrying
T-DNA insertions in any gene of interest.
89 amined the mutant phenotypes associated with
T-DNA insertions in Arabidopsis genes encoding orthologs
90 Here, we show that certain
T-DNA insertions in Arabidopsis thaliana PDIL2-1, a prot
91 T-DNA insertions in At3g50740 cause a sugar-insensitive
92 essive cpl1 and cpl3 mutations are caused by
T-DNA insertions in AtCPL1 (Arabidopsis C-terminal domai
93 We have examined Arabidopsis lines carrying
T-DNA insertions in AUXIN RESPONSE FACTOR1 (ARF1) and AR
94 gh double knockdown mutant plants containing
T-DNA insertions in both genes are embryonic lethal, und
95 Genetic mapping and analysis of
T-DNA insertions in candidate genes identified BZO1 (At1
96 hree independent homozygous mutants carrying
T-DNA insertions in CHX20 showed 35% reduction in light-
97 genetic approach to identify plants carrying
T-DNA insertions in CKI1.
98 Seeds containing
T-DNA insertions in CTF7 exhibit mitotic defects in the
99 ree triple mutants harboring non-overlapping
T-DNA insertions in cytokinin AHK receptors.
100 used forward genetics to identify duplicate
T-DNA insertions in each gene.
101 T-DNA insertions in each of these genes were identified,
102 3, nfd4, nfd5, and nfd6 mutants also contain
T-DNA insertions in genes predicted to encode proteins t
103 We found a relatively high frequency of
T-DNA insertions in heterochromatic regions, including c
104 T-DNA insertions in IRX10 gave a mild irregular xylem (i
105 Seedlings homozygous for
T-DNA insertions in KEG undergo growth arrest immediatel
106 A collection of Arabidopsis lines with
T-DNA insertions in known sites was generated to increas
107 Lines containing
T-DNA insertions in S-ACP-DES1 and S-ACP-DES4 show that
108 Three
T-DNA insertions in SEC8 cause an absolute, male-specifi
109 We have isolated
T-DNA insertions in six of the type-A ARRs and construct
110 T-DNA insertions in the Arabidopsis thaliana ortholog co
111 of AHPs in cytokinin signaling, we isolated
T-DNA insertions in the five AHP genes that are predicte
112 acid (ABA) but is increased in mutants with
T-DNA insertions in the FLDH 5' flanking region.
113 T-DNA insertions in the genes represented by some cDNAs
114 Two independent mutant lines with
T-DNA insertions in the previously identified At5g23960
115 Two independent lines with
T-DNA insertions in the promoter region of PDX3 (pdx3-1
116 er, the roots of Arabidopsis plants carrying
T-DNA insertions in the putative MeIAA esterase gene AtM
117 Plants carrying
T-DNA insertions in three AtGATL genes (atgatl3, atgatl6
118 T-DNA insertions in UKL1 and UKL2 reduced transcript exp
119 We show here that rat4 contains a
T-DNA insertion into the 3'-untranslated region of the c
120 A
T-DNA insertion into the Arabidopsis gene (At5g14090) mo
121 A
T-DNA insertion into the gene for the plastidic E2 (dihy
122 as identified through the segregation of two
T-DNA insertions into different recombinant lines, genet
123 selection pressure may shift the recovery of
T-DNA insertions into gene-rich or transcriptionally act
124 Furthermore,
T-DNA insertions into the FCLY gene cause significant de
125 t allows the large-scale characterization of
T-DNA insertions into the genome of Brachypodium.
126 Whereas depletion of B14.7 by
T-DNA insertion is lethal, Tim23-2 can be depleted witho
127 Analysis of single and higher-order
T-DNA insertion jaz null mutants provided further eviden
128 ipids accumulate in a tgd3 mutant carrying a
T-DNA insertion just 5' of the TGD3 coding region.
129 The act7-1 and act7-4 alleles contain
T-DNA insertions just after the stop codon and within th
130 T-DNA insertions just downstream of the major polyadenyl
131 For a number of QTLs,
T-DNA insertion knockout lines could validate assigned c
132 in the present study we isolated Arabidopsis
T-DNA insertion knockout mutant lines for each of the ge
133 Disruption of AtNDB2 expression via
T-DNA insertion led to a 90% decrease of external NADH o
134 as identified in a Beauveria bassiana random
T-DNA insertion library.
135 ociation (Ds) insertion line (SGT4559) and a
T-DNA insertion line (SRIE1) demonstrated that disruptio
136 Like pskr1 mutants, a tpst
T-DNA insertion line exhibited enhanced MAMP-triggered s
137 antisense AtHD1 (CASH) transgenic line and a
T-DNA insertion line in exon 2 of AtHD1, resulting in a
138 A
T-DNA insertion line in the PSB29 gene in Arabidopsis th
139 S2 in maltose metabolism, we characterized a
T-DNA insertion line of the AtPHS2 gene.
140 Finally, a homozygous
T-DNA insertion line, which lacks a functional At3g02870
141 version was expressed, indicating that these
T-DNA insertion lines are gain-of-function mutants.
142 Homozygous
T-DNA insertion lines are recovered for BRIZ1 and BRIZ2
143 From a collection of transposon and
T-DNA insertion lines at the RIKEN chloroplast function
144 Previous reports have indicated that
T-DNA insertion lines can have chromosomal translocation
145 Furthermore, the zml1 and zml2
T-DNA insertion lines displayed a high irradiance-sensit
146 nent), which on simultaneous inactivation by
T-DNA insertion lines displayed a severely delayed and c
147 t the identification and characterization of
T-DNA insertion lines for 18 of the 23 ARF gene family m
148 of more than 3700 confirmed homozygous SALK
T-DNA insertion lines for visible defects under prolonge
149 T-DNA insertion lines for ZML2 and its homolog ZML1 demo
150 atmyb2
T-DNA insertion lines have enhanced expression of cytoki
151 To discover new root-hair genes, 159
T-DNA insertion lines identified from the root-hair morp
152 hat has been used to create sequence-indexed
T-DNA insertion lines in Arabidopsis thaliana as a tool
153 a putative function of AtVDACs, we analyzed
T-DNA insertion lines in each of the corresponding genes
154 ing that disruption of BRIZ1 or BRIZ2 in the
T-DNA insertion lines is responsible for the observed ph
155 Leaf senescence in two
T-DNA insertion lines of this gene is significantly dela
156 ter-directed cytokinin oxidase 1 gene in the
T-DNA insertion lines reduces the endogenous cytokinin l
157 Creating
T-DNA insertion lines requires a dependable method for l
158 Thermotolerance assays of PME gene
T-DNA insertion lines revealed two null mutant alleles o
159 AAP2
T-DNA insertion lines showed changes in source-sink tran
160 We used Arabidopsis
T-DNA insertion lines to generate a double mutant in whi
161 Four
T-DNA insertion lines were characterized, which comprise
162 tags and microarrays, and publicly available
T-DNA insertion lines were collected.
163 More than 120,000
T-DNA insertion lines were generated following Agrobacte
164 Homozygous
T-DNA insertion lines were thus obtained for five of the
165 Here we show that mature leaves of
T-DNA insertion lines with diminished expression of PRX3
166 Two independent homozygous
T-DNA insertion lines, pp2ca-1 and pp2ca-2, were recover
167 s are present in a widely-used collection of
T-DNA insertion lines, we analyzed 64 independent lines
168 Using
T-DNA insertion lines, we isolated a novel deletion muta
169 lanking sequence tags (FST) for over 325,000
T-DNA insertion lines.
170 untapped potential in the publicly available
T-DNA insertion lines.
171 d the respective genes were identified using
T-DNA insertion lines.
172 e identified through a large-scale screen of
T-DNA insertion lines.
173 The lesion caused by the
T-DNA insertion localizes to the promoter region, result
174 The frequency with which
T-DNA insertions mapped to exon, intron, 5' upstream and
175 so developed inexpensive methods for INTACT,
T-DNA insertion mapping, and profiling of the complete n
176 The MEF8
T-DNA insertion (
mef8) line exhibited reduced editing at
177 s and by the characterization of a knock-out
T-DNA insertion mutant (glt1-T) in the single NADH-GOGAT
178 localization and the phenotypes of rh3-4, a
T-DNA insertion mutant allele of RH3.
179 Characterization of
T-DNA insertion mutant alleles at each AACT locus establ
180 d AtECA3 in Arabidopsis, several independent
T-DNA insertion mutant alleles were isolated.
181 ght, heat and aluminum stresses, whereas the
T-DNA insertion mutant erf74 and the erf74;erf75 double
182 fold to threefold in an Arabidopsis thaliana
T-DNA insertion mutant in CLPR2 designated clpr2-1.
183 A
T-DNA insertion mutant in cytosolic AAT2 (aat2-T) was al
184 perturbed L-Gal metabolism in vtc4-1 and the
T-DNA insertion mutant indicate that L-Gal-1-P phosphata
185 ilencing induced by the dcl3-1 (SALK_005512)
T-DNA insertion mutant line.
186 Thus, some
T-DNA insertion mutant lines induce 35S promoter homolog
187 homology-dependent silencing induced by some
T-DNA insertion mutant lines is siRNA-mediated.
188 The utility of many
T-DNA insertion mutant lines of Arabidopsis is compromis
189 Two Arabidopsis
T-DNA insertion mutant lines with insertions in the prom
190 reactive oxygen species were monitored in a
T-DNA insertion mutant of AHK5.
191 Seedling growth was severely reduced in a
T-DNA insertion mutant of ICE1, ice1-2, when grown on 1/
192 The
T-DNA insertion mutant of MSRB8 exaggerates HR-associate
193 Here, we describe the isolation of a
T-DNA insertion mutant of phyC (phyC-1), the subsequent
194 eport the characterization of an Arabidopsis
T-DNA insertion mutant of the MED14 gene.
195 erized an Arabidopsis (Arabidopsis thaliana)
T-DNA insertion mutant pifi (for postillumination chloro
196 RTP1 was identified by screening a
T-DNA insertion mutant population and encoded an endopla
197 HC-Pro transgenic Arabidopsis and the arf8-6
T-DNA insertion mutant showed little effect on the P1/HC
198 The presence of ascorbate in the
T-DNA insertion mutant suggests there is a bypass to thi
199 A
T-DNA insertion mutant that affects RPN12a has a decreas
200 A homozygous
T-DNA insertion mutant that does not express AtCel5 form
201 erance of an ERF74 overexpression line and a
T-DNA insertion mutant using flow cytometry, transactiva
202 Arf8-6 is a SALK line
T-DNA insertion mutant, a class of mutations prone to in
203 An Arabidopsis
T-DNA insertion mutant, vti12, had a normal phenotype un
204 t triple mutant c1,c3,fkf1-t carrying a FKF1
T-DNA insertion mutant.
205 ion transgenic lines or in the transfer-DNA (
T-DNA) insertion mutant lbd29-1, enhanced SCW developmen
206 wth attenuation in plants of a transfer DNA (
T-DNA) insertion mutant of WRKY70 (wrky70) suggest that
207 When either kinesin was knocked out by
T-DNA insertions,
mutant plants did not show a noticeabl
208 T-DNA insertion mutants (atg mutants) of these genes dis
209 er we examine callose deposition patterns in
T-DNA insertion mutants (cs7) of the Callose Synthase 7
210 We have now used TILLING and
T-DNA insertion mutants (gsl1-1, gsl5-2 and gsl5-3) to s
211 resource for information on a collection of
T-DNA insertion mutants (knockouts) in each kinase and p
212 of the wild-type level in three Arabidopsis
T-DNA insertion mutants (naa20-1, naa20-2, and naa25-1)
213 Two At5g55120
T-DNA insertion mutants (vtc5-1 and vtc5-2) have 80% of
214 Through a phenotypic analysis of
T-DNA insertion mutants affecting HO3 and HO4 in combina
215 Null
T-DNA insertion mutants affecting the single genes encod
216 pproximately 40% for Arabidopsis msr1 single
T-DNA insertion mutants and by more than 50% for msr1 ms
217 ed 126 rat mutants by screening libraries of
T-DNA insertion mutants and by using various "reverse ge
218 Rb(+) uptake kinetics in roots of athak5
T-DNA insertion mutants and wild-type plants demonstrate
219 Based on data derived from
T-DNA insertion mutants and yeast (Saccharomyces cerevis
220 T-DNA insertion mutants are a tool used widely in Arabid
221 ons of Arabidopsis thaliana sequence-indexed
T-DNA insertion mutants are among the most important res
222 N. benthamiana and Arabidopsis thaliana GOX
T-DNA insertion mutants are compromised for nonhost resi
223 Homozygous Atcdc48A
T-DNA insertion mutants arrest during seedling developme
224 e used a reverse genetics approach to screen
T-DNA insertion mutants corresponding to all 47 of the A
225 Characterization of
T-DNA insertion mutants defective in the other ACX genes
226 Analysis of rpa1
T-DNA insertion mutants demonstrates that although each
227 Detailed characterization of the
T-DNA insertion mutants des1-1 and des1-2 has provided i
228 ation of BON1/CPN1 in two BON1/CPN1 promoter
T-DNA insertion mutants did not affect resistance to a b
229 mplex has been studied using four homozygous
T-DNA insertion mutants for ARP2, ARP3, and ARPC5/p16.
230 In addition, homozygous
T-DNA insertion mutants for At LCB1 were not recoverable
231 pressing the wild type version of bZIP16 and
T-DNA insertion mutants for bZIP68 and GBF1 demonstrated
232 Analyses of
T-DNA insertion mutants for each of these candidate PSS1
233 We characterized
T-DNA insertion mutants for nine chito-oligomer responsi
234 Phenotypic analysis of homozygous
T-DNA insertion mutants for the gene At3g20570 shows min
235 T-DNA insertion mutants have been widely used to define
236 cted phenomenon of epigenetic suppression of
T-DNA insertion mutants in Arabidopsis.
237 T-DNA insertion mutants in AtGT13 and AtGT18 displayed r
238 Two independent SALK
T-DNA insertion mutants in AtPAP15 had 30% less foliar A
239 We have isolated and characterized
T-DNA insertion mutants in the medium to long-chain (ACX
240 We therefore screened
T-DNA insertion mutants in these RLKs for root hair defe
241 le of functionally complementing Arabidopsis
T-DNA insertion mutants in this gene.
242 Here we identified
T-DNA insertion mutants in three alpha subunit genes (al
243 gation analyses from two independent sets of
T-DNA insertion mutants indicate that a double disruptio
244 o transport measurements, analyses of atmrp1
T-DNA insertion mutants of Arabidopsis ecotypes Wassilew
245 yme in vivo, we identified three independent
T-DNA insertion mutants of AtPARN which interrupt the ge
246 T-DNA insertion mutants of CIAF1 lack Complex I and the
247 ulate dramatically at high temperatures, the
T-DNA insertion mutants of ClpB-p and ClpB-m show no evi
248 Finally, phenotypic analysis of
T-DNA insertion mutants of genes identified in this anal
249 Functional studies using
T-DNA insertion mutants reveal that they can act as anti
250 vity of CPL2 DRM has not been shown to date,
T-DNA insertion mutants that express CPL2 variants lacki
251 Two Arabidopsis
T-DNA insertion mutants were identified as null mutants
252 Etiolated
T-DNA insertion mutants were screened for red fluorescen
253 Compared with the wild type, WRKY22
T-DNA insertion mutants wrky22-1 and wrky22-2 had lower
254 These
T-DNA insertion mutants, called fldh-1 and fldh-2, are a
255 Plants of
T-DNA insertion mutants, lacking FUM2, show marked diffe
256 sing the newly isolated rgl1, rgl2, and rgl3
T-DNA insertion mutants, we demonstrated that RGL2 is th
257 Using Arabidopsis
T-DNA insertion mutants, we found that their Arabidopsis
258 When the two
T-DNA insertion mutants, yuc1-1 and ag-TD, were crossed
259 ed xxt1 and xxt2 single and xxt1 xxt2 double
T-DNA insertion mutants.
260 pression and the phenotypes of corresponding
T-DNA insertion mutants.
261 ovement in response to root flooding in aco5
T-DNA insertion mutants.
262 een a collection of individual transfer DNA (
T-DNA) insertion mutants.
263 ts failed to rescue the respective knockout (
T-DNA insertion)
mutants, indicating that pigment-bindin
264 Homozygous plants carrying a
T-DNA insertion mutation in AtSPP, spp-2, could not be r
265 athway mutations, including a newly isolated
T-DNA insertion mutation in the gene encoding the ethyle
266 We have identified a
T-DNA insertion mutation of Arabidopsis (ecotype C24), n
267 T-DNA insertion mutations in ACA10, but not in the two o
268 T-DNA insertion mutations in ADA2b and GCN5 were found t
269 of these genes by salt stress was blocked by
T-DNA insertion mutations in AtS1P and AtbZIP17.
270 Here, we report the effects of
T-DNA insertion mutations in the Arabidopsis GGB gene, w
271 or the repair of DSBs in plants, we isolated
T-DNA insertion mutations in the Arabidopsis homologs of
272 Two independent heterozygous lines with
T-DNA insertion on the AtCPSF73-II gene also showed the
273 lt plant while knocking down miR408 level by
T-DNA insertions or the artificial miRNA technique cause
274 itional analyses with Arabidopsis containing
T-DNA insertion (
pbs3-2) and transposon insertion (pbs3-
275 Two hot5 missense alleles and two
T-DNA insertion,
protein null alleles were characterized
276 T-DNA insertion rates were also decreased in the mutants
277 Disruption of AtPLAI by
T-DNA insertion reduced the basal level of JA, but did n
278 These
T-DNA insertion regions are disfavored under selective c
279 genes during zinc deficiency, and the WAKL4
T-DNA insertion resulted in a reduction of Zn2+ accumula
280 Knockout mutations of the CalS5 gene by
T-DNA insertion resulted in a severe reduction in fertil
281 Disruption of AtPAT14 by
T-DNA insertion resulted in an accelerated senescence ph
282 Disruption of the Thf1 gene via
T-DNA insertion results in plants that are severely stun
283 Missense (shot1-1) and
T-DNA insertion (
shot1-2) mutants suppress the hot1-4 he
284 nt plants with the CYP38 gene interrupted by
T-DNA insertion showed stunted growth and were hypersens
285 Plants homozygous for pskr1
T-DNA insertions showed enhanced defense gene expression
286 One of these lines, BME3, had a
T-DNA insertion site in the 5' upstream region of a GATA
287 romosomal translocations associated with the
T-DNA insertion site, but the prevalence of these rearra
288 Predicted
T-DNA insertion sites, when mapped, showed a bias agains
289 Loss-of-function
T-DNA insertion siz1-2 and siz1-3 mutations caused ABA h
290 during the embryonic phase, plants carrying
T-DNA insertions that disrupt these genes were isolated.
291 Phenotypic analyses of lines that contain
T-DNA insertions to individual mei2 -like genes reveal n
292 Analyses of
T-DNA insertion victr alleles showed that VICTR is neces
293 meiotic recombination between tightly linked
T-DNA insertions was developed to generate Arabidopsis t
294 CML38-knockout mutants generated via
T-DNA insertion were insensitive to AtRALF1, and simulta
295 T-DNA insertions were identified in four of the five Ara
296 was revealed by knocking down GF14lambda by
T-DNA insertion,
which compromised basal and RPW8-mediat
297 immediately flanking the right border of the
T-DNA insertion,
which encoded an uncharacterized Broad
298 cations were determined for more than 88,000
T-DNA insertions,
which resulted in the identification o
299 that these constructs could produce targeted
T-DNA insertions with frequencies ranging between 4 and
300 in plant growth and development, we isolated
T-DNA insertions within six of the genes (ARR1, ARR2, AR