2006
DOI: 10.1105/tpc.106.043158
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Tobacco Tsip1, a DnaJ-Type Zn Finger Protein, Is Recruited to and Potentiates Tsi1-Mediated Transcriptional Activation

Abstract: Tobacco stress-induced1 (Tsi1) is an ethylene-responsive-element binding protein/APETALA2-type transcription factor that plays an important role in both biotic and abiotic stress signaling pathways. We show that Tsi1-interacting protein1 (Tsip1), a DnaJ-type Zn finger protein, interacts with Tsi1 in vitro and in yeast (Saccharomyces cerevisiae). The transcript level of Tsip1 in tobacco (Nicotiana tabacum) increased upon treatment with salicylic acid (SA), ethylene, gibberellic acid, NaCl, and virus challenge. … Show more

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Cited by 58 publications
(69 citation statements)
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“…Isolation of NtTfd1 as a Tsip1-interacting protein by yeast two-hybrid screening Tsip1 was identified as a transcriptional co-activator by interaction with EREBP/AP2-type transcription factor Tsi1 (Ham et al, 2006;Park et al, 2001). To carry out further functional study of Tsip1, we performed yeast two-hybrid screening of tobacco cDNA library using Tsip1 as bait.…”
Section: Resultsmentioning
confidence: 99%
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“…Isolation of NtTfd1 as a Tsip1-interacting protein by yeast two-hybrid screening Tsip1 was identified as a transcriptional co-activator by interaction with EREBP/AP2-type transcription factor Tsi1 (Ham et al, 2006;Park et al, 2001). To carry out further functional study of Tsip1, we performed yeast two-hybrid screening of tobacco cDNA library using Tsip1 as bait.…”
Section: Resultsmentioning
confidence: 99%
“…Tsip1 is a transcriptional co-activator of an EREBP/AP2-type transcription factor, Tsi1 (for Tobacco stress-induced gene 1), and relocalizes with Tsi1 to the nucleus from the chloroplast upon salicylic acid treatment (Ham et al, 2006;Park et al, 2001). The protein relocalization in response to biotic and abiotic stress signals are relatively common in plants (Caplan et al, 2008;Hwang and Sheen, 2001;Igarashi et al, 2001;Yeung et al, 2008) and could have evolved as a defense mechanism of plants to pathogens and environmental stresses.…”
Section: Introductionmentioning
confidence: 99%
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“…Arabidopsis wildtype and transgenic plants had the ecotype Columbia-0 background and were grown in a 16 h light/8 h dark photoperiod at 23°C in soil. For the constitutive expression of APUM5 (At3g20250), a modified pCAMBIA2300 vector was used (25), and the APUM5 ORF was amplified using Pfu DNA polymerase (Promega) and cloned. For the repression of APUM5 expression, the RNAi technique was exploited using the pHANNIVAL vector system, which can transcribe self-complementary hairpin RNA molecules (26).…”
Section: Methodsmentioning
confidence: 99%