Xanthomonas AvrBs3 Family-Type III Effectors: Discovery and Function

The plant immune system

Jones, J. D. G., & Dangl, J. L. (2006) · Nature · doi:10.1038/nature05286 · Cited by 13,177 · see citing works

Breaking the Code of DNA Binding Specificity of TAL-Type III Effectors

Boch, J., Scholze, H., Schornack, S., Landgraf, A., Hahn, S., Kay, S., Lahaye, T., Nickstadt, A., & Bonas, U. (2009) · Science · doi:10.1126/science.1178811 · Cited by 2,707 · see citing works

A Simple Cipher Governs DNA Recognition by TAL Effectors

Moscou, M., & Bogdanove, A. J. (2009) · Science · doi:10.1126/science.1178817 · Cited by 1,992 · see citing works

TPR proteins: the versatile helix

D’Andrea, L. D. (2003) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2003.10.007 · Cited by 1,154 · see citing works

Methylation as a Crucial Step in Plant microRNA Biogenesis

Yu, B., Yang, Z., Li, J., Minakhina, S., Yang, M., Padgett, R. W., Steward, R., & Chen, X. (2005) · Science · doi:10.1126/science.1107130 · Cited by 1,135 · see citing works

Co-crystal structure of TBP recognizing the minor groove of a TATA element

Kim, J. L., Nikolov, D. B., & Burley, S. K. (1993) · Nature · doi:10.1038/365520a0 · Cited by 1,047 · see citing works

Pentatricopeptide repeat proteins: a socket set for organelle gene expression

Schmitz‐Linneweber, C., & Small, I. (2008) · Trends in Plant Science · doi:10.1016/j.tplants.2008.10.001 · Cited by 825 · see citing works

Enhancing Gene Targeting with Designed Zinc Finger Nucleases

Bibikova, M. V., Beumer, K. J., Trautman, J. K., & Carroll, D. (2003) · Science · doi:10.1126/science.1079512 · Cited by 824 · see citing works

From Guard to Decoy: A New Model for Perception of Plant Pathogen Effectors

van der Hoorn, R. A. L., & Kamoun, S. (2008) · The Plant Cell · doi:10.1105/tpc.108.060194 · Cited by 783 · see citing works

Emerging Concepts in Effector Biology of Plant-Associated Organisms

Hogenhout, S. A., van der Hoorn, R. A. L., Terauchi, R., et al. (2009) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-22-2-0115 · Cited by 763 · see citing works

Chimeric nucleases stimulate gene targeting in human cells

Porteus, M. H., & Baltimore, D. (2003) · Science · doi:10.1126/science.1078395 · Cited by 741 · see citing works

Rapid “Open-Source” Engineering of Customized Zinc-Finger Nucleases for Highly Efficient Gene Modification

Maeder, M. L., Thibodeau-Beganny, S., Osiak, A., Wright, D. A., Anthony, R. M., Eichtinger, M., Jiang, T., Foley, J. E., Winfrey, R. J., Townsend, J. A., et al. (2008) · Molecular Cell · doi:10.1016/j.molcel.2008.06.016 · Cited by 708 · see citing works

Os8N3 is a host disease-susceptibility gene for bacterial blight of rice

Yang, B., Sugio, A., & White, F. F. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604088103 · Cited by 635 · see citing works

A Bacterial Effector Acts as a Plant Transcription Factor and Induces a Cell Size Regulator

Kay, S., Hahn, S., Marois, É., et al. (2007) · Science · doi:10.1126/science.1144956 · Cited by 594 · see citing works

R gene expression induced by a type-III effector triggers disease resistance in rice

Gu, K., Yang, B., Tian, D., et al. (2005) · Nature · doi:10.1038/nature03630 · Cited by 578 · see citing works

microRNA biogenesis and function in plants

Chen, X. (2005) · FEBS Letters · doi:10.1016/j.febslet.2005.07.071 · Cited by 565 · see citing works

Promoter mutations of an essential gene for pollen development result in disease resistance in ricePreprint

Chu, Z., Yuan, M., Yao, J., et al. (2006) · Genes & Development · doi:10.1101/gad.1416306 · Cited by 561 · see citing works

Regulation and secretion of Xanthomonas virulence factors

Büttner, D., & Bonas, U. (2009) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2009.00192.x · Cited by 555 · see citing works

Plant Pathogen Recognition Mediated by Promoter Activation of the Pepper Bs3 Resistance Gene

Römer, P., Hahn, S., Jordan, T., et al. (2007) · Science · doi:10.1126/science.1144958 · Cited by 470 · see citing works

The genome sequence of Xanthomonas oryzae pathovar oryzae KACC10331, the bacterial blight pathogen of rice

Lee, B.-M. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki206 · Cited by 447 · see citing works

Crystal structure of TFIID TATA-box binding protein

Nikolov, D. B., Hu, S., Lin, J., et al. (1992) · Nature · doi:10.1038/360040a0 · Cited by 411 · see citing works

Suppression of the MicroRNA Pathway by Bacterial Effector Proteins

Navarro, L., Jay, F., Nomura, K., He, S. Y., & Voinnet, O. (2008) · Science · doi:10.1126/science.1159505 · Cited by 397 · see citing works

Cloned avirulence gene of Pseudomonas syringae pv. glycinea determines race-specific incompatibility on Glycine max (L.) Merr

Staskawicz, B. J., Dahlbeck, D., & Keen, N. T. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.19.6024 · Cited by 394 · see citing works

Genetic and structural characterization of the avirulence gene avrBs3 from Xanthomonas campestris pv. vesicatoria

Bonas, U., Stall, R. E., & Staskawicz, B. J. (1989) · Molecular and General Genetics MGG · doi:10.1007/bf00330575 · Cited by 393 · see citing works

The type III effectors of Xanthomonas

White, F. F., Potnis, N., Jones, J. B., et al. (2009) · Molecular Plant Pathology · doi:10.1111/j.1364-3703.2009.00590.x · Cited by 384 · see citing works

Recognition of the Bacterial Avirulence Protein AvrBs3 Occurs inside the Host Plant Cell

den Ackerveken, G. F. J. M. V., Marois, É., & Bonas, U. (1996) · Cell · doi:10.1016/s0092-8674(00)81825-5 · Cited by 363 · see citing works

The Rice Bacterial Blight Resistance Gene xa5 Encodes a Novel Form of Disease Resistance

Iyer‐Pascuzzi, A. S., & McCouch, S. R. (2004) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2004.17.12.1348 · Cited by 357 · see citing works

Insights into Genome Plasticity and Pathogenicity of the Plant Pathogenic BacteriumXanthomonas campestrispv. vesicatoria Revealed by the Complete Genome Sequence

Thieme, F., Koebnik, R., Bekel, T., Berger, C., Boch, J., Büttner, D., Caldana, C., Gaigalat, L., Goesmann, A., Kay, S., et al. (2005) · Journal of Bacteriology · doi:10.1128/jb.187.21.7254-7266.2005 · Cited by 346 · see citing works

RUPTURED POLLEN GRAIN1 , a Member of the MtN3/saliva Gene Family, Is Crucial for Exine Pattern Formation and Cell Integrity of Microspores in Arabidopsis

Guan, Y., Huang, X.-Y., Zhu, J., et al. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.118026 · Cited by 294 · see citing works

Predicting durability of a disease resistance gene based on an assessment of the fitness loss and epidemiological consequences of avirulence gene mutation

Cruz, C. V., Bai, J., Oña, I., et al. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.250271997 · Cited by 294 · see citing works

The chickenRaxLgene plays a role in the initiation of photoreceptor differentiation

Chen, C.-M. A., & Cepko, C. L. (2002) · Development · doi:10.1242/dev.00114 · Cited by 293 · see citing works

Crystal structure of a human TATA box-binding protein/TATA element complex.

Nikolov, D. B., Chen, H., Halay, E. D., et al. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.10.4862 · Cited by 289 · see citing works

When protein folding is simplified to protein coiling: the continuum of solenoid protein structures

Kobe, B., & Kajava, A. V. (2000) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(00)01667-4 · Cited by 281 · see citing works

Use of a Subtractive Hybridization Approach to Identify New Medicago truncatula Genes Induced During Root Nodule Development

Gamas, P. (1996) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-9-0233 · Cited by 280 · see citing works

HrpXv, an AraC-type regulator, activates expression of five of the six loci in the hrp cluster of Xanthomonas campestris pv. vesicatoria

Wengelnik, K., & Bonas, U. (1996) · Journal of Bacteriology · doi:10.1128/jb.178.12.3462-3469.1996 · Cited by 279 · see citing works

Gene-For-Gene Relationships Specifying Disease Resistance in Xanthomonas campestris pv. vesicatoria - Pepper Interactions

Minsavage, G. V. (1990) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-3-041 · Cited by 277 · see citing works

Identification of a Family of Avirulence Genes fromXanthomonas oryzaepv.oryzae

Hopkins, C. M. (1992) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-5-451 · Cited by 276 · see citing works

How Xanthomonas type III effectors manipulate the host plant

Kay, S., & Bonas, U. (2009) · Current Opinion in Microbiology · doi:10.1016/j.mib.2008.12.006 · Cited by 268 · see citing works

HrpG, a Key hrp Regulatory Protein of Xanthomonas campestris pv. vesicatoria Is Homologous to Two-Component Response Regulators

Wengelnik, K. (1996) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-9-0704 · Cited by 247 · see citing works

Genome Sequence of Xanthomonas oryzae pv. oryzae Suggests Contribution of Large Numbers of Effector Genes and Insertion Sequences to Its Race Diversity

Ochiai, H., INOUE, Y., Takeya, M., et al. (2005) · Japan Agricultural Research Quarterly JARQ · doi:10.6090/jarq.39.275 · Cited by 242 · see citing works

Getting across—bacterial type III effector proteins on their way to the plant cell

Büttner, D., & Bonas, U. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf536 · Cited by 238 · see citing works

Inventory and functional analysis of the large Hrp regulon in Ralstonia solanacearum : identification of novel effector proteins translocated to plant host cells through the type III secretion system

Cunnac, S., Occhialini, A., Barberis, P., et al. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04118.x · Cited by 233 · see citing works

Targeting xa13, a recessive gene for bacterial blight resistance in rice

Chu, Z., Fu, B., Yang, H. Y., Xu, C., Li, Z., Sanchez, A., Park, Y., Bennetzen, J. L., Zhang, Q., & Wang, S. (2005) · Theoretical and Applied Genetics · doi:10.1007/s00122-005-0145-6 · Cited by 232 · see citing works

Two type III effector genes of Xanthomonas oryzae pv. oryzae control the induction of the host genes OsTFIIA γ 1 and OsTFX1 during bacterial blight of rice

Sugio, A., Yang, B., Zhu, T., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0701742104 · Cited by 228 · see citing works

Port of entry – the type III secretion translocon

Büttner, D., & Bonas, U. (2002) · Trends in Microbiology · doi:10.1016/s0966-842x(02)02331-4 · Cited by 226 · see citing works

The Xanthomonas Type III Effector Protein AvrBs3 Modulates Plant Gene Expression and Induces Cell Hypertrophy in the Susceptible Host

Marois, É., den Ackerveken, G. F. J. M. V., & Bonas, U. (2002) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2002.15.7.637 · Cited by 221 · see citing works

Diverse Members of the AvrBs3/PthA Family of Type III Effectors Are Major Virulence Determinants in Bacterial Blight Disease of Rice

Yang, B., & White, F. F. (2004) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2004.17.11.1192 · Cited by 221 · see citing works

AnXanthomonas citriPathogenicity Gene,pthA,Pleiotropically Encodes Gratuitous Avirulence on Nonhosts

Swarup, S. (1992) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-5-204 · Cited by 212 · see citing works

HEN1functions pleiotropically inArabidopsisdevelopment and acts in C function in the flower

Chen, X., Liu, J., Cheng, Y., & Jia, D. (2002) · Development · doi:10.1242/dev.129.5.1085 · Cited by 209 · see citing works

The tomato resistance protein Bs4 is a predicted non‐nuclear TIR‐NB‐LRR protein that mediates defense responses to severely truncated derivatives of AvrBs4 and overexpressed AvrBs3

Schornack, S., Ballvora, A., Gürlebeck, D., et al. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01937.x · Cited by 208 · see citing works

The virulence factor AvrXa7 of Xanthomonas oryzae pv . oryzae is a type III secretion pathway-dependent nuclear-localized double-stranded DNA-binding protein

Yang, B., Zhu, W., Johnson, L. B., et al. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.170286897 · Cited by 208 · see citing works

Host and Pathogen Factors Controlling the Rice-Xanthomonas oryzae Interaction

White, F. F., & Yang, B. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.139360 · Cited by 206 · see citing works

Promoter elements of rice susceptibility genes are bound and activated by specific TAL effectors from the bacterial blight pathogen, Xanthomonas oryzae pv. oryzae

Römer, P., Recht, S., Strauß, T., et al. (2010) · New Phytologist · doi:10.1111/j.1469-8137.2010.03217.x · Cited by 204 · see citing works

Isolation of a Gene Cluster from Xanthomonas campestris pv. vesicatoria that Determines Pathogenicity and the Hypersensitive Response on Pepper and Tomato

Bonas, U. (1991) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-4-081 · Cited by 200 · see citing works

To Nibble at Plant Resistance Proteins

Takken, F. L. W., & Tameling, W. I. L. (2009) · Science · doi:10.1126/science.1171666 · Cited by 196 · see citing works

AvrXa10 Contains an Acidic Transcriptional Activation Domain in the Functionally Conserved C Terminus

Zhu, W., Yang, B., Chittoor, J. M., Johnson, L. B., & White, F. F. (1998) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.1998.11.8.824 · Cited by 193 · see citing works

Prospects for understanding avirulence gene function

White, F. F., Yang, B., & Johnson, L. B. (2000) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(00)00082-0 · Cited by 187 · see citing works

The complete genome sequence of Xanthomonas albilineans provides new insights into the reductive genome evolution of the xylem-limited Xanthomonadaceae

Pieretti, I., Royer, M., Barbe, V., et al. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-616 · Cited by 184 · see citing works

XanthomonasAvirulence/Pathogenicity Gene Family Encodes Functional Plant Nuclear Targeting Signals

Yang, Y. (1995) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-8-0627 · Cited by 180 · see citing works

A Pathogenicity Locus fromXanthomonas citriEnables Strains from Several Pathovars ofX. campestristo Elicit Cankerlike Lesions on Citrus

Swarup, S. (1991) · Phytopathology · doi:10.1094/phyto-81-802 · Cited by 180 · see citing works

Eukaryotic features of the Xanthomonas type III effector AvrBs3: protein domains involved in transcriptional activation and the interaction with nuclear import receptors from pepper

Szurek, B., Marois, É., Bonas, U., et al. (2001) · The Plant Journal · doi:10.1046/j.0960-7412.2001.01046.x · Cited by 178 · see citing works

Race-specificity of plant resistance to bacterial spot disease determined by repetitive motifs in a bacterial avirulence protein

Herbers, K., Conrads-Strauch, J., & Bonas, U. (1992) · Nature · doi:10.1038/356172a0 · Cited by 170 · see citing works

High-resolution genetic mapping of Xa27(t), a new bacterial blight resistance gene in rice, Oryza sativa L.

Gu, K., Tian, D., Yang, F., et al. (2003) · Theoretical and Applied Genetics · doi:10.1007/s00122-003-1491-x · Cited by 167 · see citing works

Type III‐dependent translocation of the Xanthomonas AvrBs3 protein into the plant cell

Szurek, B., Rossier, O., Hause, G., et al. (2002) · Molecular Microbiology · doi:10.1046/j.1365-2958.2002.03139.x · Cited by 164 · see citing works

Gene-for-gene-mediated recognition of nuclear-targeted AvrBs3-like bacterial effector proteins

Schornack, S., Meyer, A., Römer, P., Jordan, T., & Lahaye, T. (2006) · Journal of Plant Physiology · doi:10.1016/j.jplph.2005.12.001 · Cited by 164 · see citing works

A single plant resistance gene promoter engineered to recognize multiple TAL effectors from disparate pathogens

Römer, P., Recht, S., & Lahaye, T. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0908812106 · Cited by 157 · see citing works

Structural insights into mechanisms of the small RNA methyltransferase HEN1

Huang, Y., Ji, L., Huang, Q., et al. (2009) · Nature · doi:10.1038/nature08433 · Cited by 153 · see citing works

Expression of a Single, Host-Specific, Bacterial Pathogenicity Gene in Plant Cells Elicits Division, Enlargement, and Cell Death

Duan, Y. P., Castañeda, A., Zhao, G., et al. (1999) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.1999.12.6.556 · Cited by 148 · see citing works

Testifying the rice bacterial blight resistance gene xa5 by genetic complementation and further analyzing xa5 (Xa5) in comparison with its homolog TFIIAγ1

Jiang, G., Xia, Z., Zhou, Y., et al. (2006) · Molecular Genetics and Genomics · doi:10.1007/s00438-005-0091-7 · Cited by 143 · see citing works

Host-Specific Symptoms and Increased Release ofXanthomonas citriand X.campestrispv.malvacearumfrom Leaves Are Determined by the 102-bp Tandem Repeats ofpthAandavrb6,Respectively

Yang, Y. (1994) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-7-0345 · Cited by 126 · see citing works

Expression of the avirulence gene avrBs3 from Xanthomonas campestris pv. vesicatoria is not under the control of hrp genes and is independent of plant factors

Knoop, V., Staskawicz, B. J., & Bonas, U. (1991) · Journal of Bacteriology · doi:10.1128/jb.173.22.7142-7150.1991 · Cited by 119 · see citing works

Kinetic Studies of Fos·Jun·DNA Complex Formation: DNA Binding Prior to Dimerization

Kohler, J. J., & Schepartz, A. (2000) · Biochemistry · doi:10.1021/bi001881p · Cited by 118 · see citing works

Recognition of AvrBs3-Like Proteins Is Mediated by Specific Binding to Promoters of Matching Pepper Bs3 Alleles

Römer, P., Strauß, T., Hahn, S., et al. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.139931 · Cited by 115 · see citing works

Pathogen-Induced Expressional Loss of Function is the Key Factor in Race-Specific Bacterial Resistance Conferred by a Recessive R Gene xa13 in Rice

Yuan, M., Chu, Z., Li, X., et al. (2009) · Plant and Cell Physiology · doi:10.1093/pcp/pcp046 · Cited by 112 · see citing works

Watersoaking Functlon(s) of XcmH1005 Are Redundantly Encoded by Members of theXanthomonas avr/pthGene Family

Yang, Y. (1996) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-9-0105 · Cited by 112 · see citing works

Plant pathogenic bacteria : genomics and molecular biology

Jackson, R. W. (2009) · Caister Academic eBooks · Cited by 106 · see citing works

Detailed analysis of the DNA recognition motifs of the Xanthomonas type III effectors AvrBs3 and AvrBs3Δrep16

Kay, S., Hahn, S., Marois, É., et al. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03922.x · Cited by 105 · see citing works

Resistance in tomato to Xanthomonas campestris pv vesicatoria is determined by alleles of the pepper-specific avirulence gene avrBs3

Bonas, U., Conrads-Strauch, J., & Balbo, I. (1993) · Molecular and General Genetics MGG · doi:10.1007/bf00279555 · Cited by 99 · see citing works

Characterization of AvrHah1, a novel AvrBs3‐like effector from Xanthomonas gardneri with virulence and avirulence activity

Schornack, S., Minsavage, G. V., Stall, R. E., et al. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02487.x · Cited by 99 · see citing works

HpaB from Xanthomonas campestris pv. vesicatoria acts as an exit control protein in type III‐dependent protein secretion

Büttner, D., Gürlebeck, D., Noël, L. D., et al. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04302.x · Cited by 91 · see citing works

Genetic Mapping and Functional Analysis of the Tomato Bs4 Locus Governing Recognition of the Xanthomonas campestris pv. vesicatoria AvrBs4 Protein

Ballvora, A., Pierre, M., den Ackerveken, G. F. J. M. V., et al. (2001) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2001.14.5.629 · Cited by 90 · see citing works

The C Terminus of AvrXa10 Can Be Replaced by the Transcriptional Activation Domain of VP16 from the Herpes Simplex Virus

Zhu, W., Yang, B., Wills, N., Johnson, L. B., & White, F. F. (1999) · The Plant Cell · doi:10.1105/tpc.11.9.1665 · Cited by 90 · see citing works

XopC and XopJ, Two Novel Type III Effector Proteinsfrom Xanthomonas campestris pv.vesicatoria

Noël, L. D., Thieme, F., Gäbler, J., et al. (2003) · Journal of Bacteriology · doi:10.1128/jb.185.24.7092-7102.2003 · Cited by 88 · see citing works

Effector Genes ofXanthamonas axonopodispv.vesicatoriaPromote Transmission and Enhance Other Fitness Traits in the Field

Wichmann, G., & Bergelson, J. M. (2004) · Genetics · doi:10.1534/genetics.166.2.693 · Cited by 83 · see citing works

Recessive Resistance Genes and the Oryza sativa-Xanthomonas oryzae pv. oryzae Pathosystem

Iyer‐Pascuzzi, A. S., & McCouch, S. R. (2007) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-20-7-0731 · Cited by 78 · see citing works

Characterization of AvrBs3-Like Effectors from a Brassicaceae Pathogen Reveals Virulence and Avirulence Activities and a Protein with a Novel Repeat Architecture

Kay, S., Boch, J., & Bonas, U. (2005) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-18-0838 · Cited by 76 · see citing works

The Type III-Dependent Hrp Pilus Is Required for Productive Interaction of Xanthomonas campestris pv. vesicatoria with Pepper Host Plants

Weber, E., Ojanen‐Reuhs, T., Huguet, E., et al. (2005) · Journal of Bacteriology · doi:10.1128/jb.187.7.2458-2468.2005 · Cited by 73 · see citing works

In Planta Horizontal Transfer of a Major Pathogenicity Effector Gene

Yacoubi, B. E., Brunings, A. M., Yuan, Q., et al. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.00261-06 · Cited by 71 · see citing works

Transcription activator‐like type III effector AvrXa27 depends on OsTFIIAγ5 for the activation of Xa27 transcription in rice that triggers disease resistance to Xanthomonas oryzae pv. oryzae

Gu, K., Tian, D., Qiu, C., et al. (2009) · Molecular Plant Pathology · doi:10.1111/j.1364-3703.2009.00567.x · Cited by 70 · see citing works

Dimerization of the bacterial effector protein AvrBs3 in the plant cell cytoplasm prior to nuclear import

Gürlebeck, D., Szurek, B., & Bonas, U. (2005) · The Plant Journal · doi:10.1111/j.1365-313x.2005.02370.x · Cited by 62 · see citing works

A Gene fromXanthomonas campestrispv.vesicatoriathat Determines Avirulence in Tomato Is Related toavrBs3

Canteros, B. I. (1991) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-4-628 · Cited by 59 · see citing works

Molecular phylogenetics and comparative modeling of HEN1, a methyltransferase involved in plant microRNA biogenesis

Tkaczuk, K. L., Obarska, A., & Bujnicki, J. M. (2006) · BMC Evolutionary Biology · doi:10.1186/1471-2148-6-6 · Cited by 57 · see citing works

XA27 Depends on an Amino-Terminal Signal-Anchor-Like Sequence to Localize to the Apoplast for Resistance to Xanthomonas oryzae pv oryzae

Wu, L., Goh, M. T., Chellamma, S., et al. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.123356 · Cited by 55 · see citing works

Genetic and Functional Characterization of the Rice Bacterial Blight Disease Resistance Gene xa5

Iyer‐Pascuzzi, A. S., Jiang, H., Huang, L., et al. (2008) · Phytopathology · doi:10.1094/phyto-98-3-0289 · Cited by 52 · see citing works

A facelift for the general transcription factor TFIIA

Høiby, T., Zhou, H., Mitsiou, D. J., et al. (2007) · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · doi:10.1016/j.bbaexp.2007.04.008 · Cited by 52 · see citing works

Repeat Domain Diversity of avrBs3 -Like Genes in Ralstonia solanacearum Strains and Association with Host Preferences in the Field

Heuer, H., Yin, Y.-N., Xue, Q.-Y., et al. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.00367-07 · Cited by 51 · see citing works

TFIIA Changes the Conformation of the DNA in TBP/TATA Complexes and Increases their Kinetic Stability

Hieb, A. R., Halsey, W. A., Betterton, M. D., et al. (2007) · Journal of Molecular Biology · doi:10.1016/j.jmb.2007.06.061 · Cited by 50 · see citing works

Engineering proteins that bind, move, make and break DNA

Collins, C. H., Yokobayashi, Y., Umeno, D., et al. (2003) · Current Opinion in Biotechnology · doi:10.1016/s0958-1669(03)00091-0 · Cited by 35 · see citing works

Constitutive heterologous expression of avrXa27 in rice containing the R gene Xa27 confers enhanced resistance to compatible Xanthomonas oryzae strains

Tian, D., & Yin, Z. (2008) · Molecular Plant Pathology · doi:10.1111/j.1364-3703.2008.00509.x · Cited by 28 · see citing works

CRISPR-Cas systems for editing, regulating and targeting genomes

Sander, J. D., & Joung, J. K. (2014) · Nature Biotechnology · doi:10.1038/nbt.2842 · Cited by 3,153 · see citing works

A TALE nuclease architecture for efficient genome editing

Miller, J. C., Tan, S., Qiao, G., Barlow, K. A., Wang, J., Xia, D. F., Meng, X., Paschon, D. E., Leung, E., Hinkley, S. J., et al. (2011) · Nature Biotechnology · doi:10.1038/nbt.1755 · Cited by 2,098 · see citing works

TALENs: A widely applicable technology for targeted genome editing

Joung, J. K., & Sander, J. D. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3486 · Cited by 1,650 · see citing works

TAL effectors: customizable proteins for DNA targeting

Bogdanove, A. J., & Voytas, D. F. (2011) · Science · doi:10.1126/science.1204094 · Cited by 984 · see citing works

Differential integrity of TALE nuclease genes following adenoviral and lentiviral vector gene transfer into human cells

Holkers, M., Maggio, I., Liu, J., Janssen, J. M., Miselli, F., Mussolino, C., Recchia, A., Cathomen, T., & Gonçalves, M. A. F. V. (2013) · Nucleic Acids Research · doi:10.1093/nar/gks1446 · Cited by 312 · see citing works

Genetic engineering of microalgae for enhanced biorefinery capabilities

Fayyaz, M., Chew, K. W., Show, P. L., Ling, T. C., Ng, I.-S., & Chang, J.-S. (2020) · Biotechnology Advances · doi:10.1016/j.biotechadv.2020.107554 · Cited by 225 · see citing works

Site-directed nucleases: a paradigm shift in predictable, knowledge-based plant breeding

Podevin, N., Davies, H. V., Hartung, F., Nogué, F., & Casacuberta, J. M. (2013) · Trends in biotechnology · doi:10.1016/j.tibtech.2013.03.004 · Cited by 214 · see citing works

Newer Gene Editing Technologies toward HIV Gene Therapy

Manjunath, N., Yi, G., Dang, Y., & Shankar, P. (2013) · Viruses · doi:10.3390/v5112748 · Cited by 77 · see citing works

Genome editing and improvement of abiotic stress tolerance in crop plants

Yadav, R. K., Tripathi, M. K., Tiwari, S., Tripathi, N., Asati, R., Chauhan, S., Tiwari, P. N., & Payasi, D. K. (2023) · Life · doi:10.3390/life13071456 · Cited by 75 · see citing works

CRISPR for accelerating genetic gains in under-utilized crops of the drylands: progress and prospects

Sharma, K. K., Palakolanu, S. R., Bhattacharya, J., Shankhapal, A. R., & Bhatnagar-Mathur, P. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.999207 · Cited by 24 · see citing works

Application of artificial scaffold systems in microbial metabolic engineering

Liu, N., Dong, W., Yang, H., Li, J.-H., & Chiu, T.-Y. (2023) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2023.1328141 · Cited by 16 · see citing works

High-Throughput Screening of Type III Secretion Determinants Reveals a Major Chaperone-Independent Pathway

Ernst, N. H., Reeves, A. Z., Ramseyer, J. E., et al. (2018) · mBio · doi:10.1128/mbio.01050-18 · Cited by 24 · see citing works

The Shigella flexneri Type Three Secretion System Employs Both Chaperone‐Dependent and Noncanonical Chaperone‐Independent Pathways

Ramseyer, J. E., Ernst, N. H., Scarpetti, L., et al. (2019) · The FASEB Journal · doi:10.1096/fasebj.2019.33.1_supplement.461.16

Structure of the Type III Secretion Effector Protein ExoU in Complex with Its Chaperone SpcU

Halavaty, A. S., Borek, D., Tyson, G. H., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049388 · Cited by 41 · see citing works

Translocation of Effectors: Revisiting the Injectosome Model

Sal‐Man, N., Croxen, M. A., & Finlay, B. B. (2011) · Future Microbiology · doi:10.2217/fmb.11.33 · Cited by 2 · see citing works

Regulation of Effector Delivery by Type III Secretion Chaperone Proteins in Erwinia amylovora

Castiblanco, L. F., Triplett, L. R., & Sundin, G. W. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.00146 · Cited by 21 · see citing works