TY - JOUR
T1 - LucTrap vectors are tools to generate luciferase fusions for the quantification of transcript and protein abundance in vivo
AU - Calderon-Villalobos, Luz Irina A.
AU - Kuhnle, Carola
AU - Li, Hanbing
AU - Rosso, Mario
AU - Weisshaar, Bernd
AU - Schwechheimer, Claus
PY - 2006/5
Y1 - 2006/5
N2 - Proper plant growth and development strongly rely on the plant's ability to respond dynamically to signals and cues from the intra- and extracellular environment. Whereas many of these responses require specific changes at the level of gene expression, in recent years it has become increasingly clear that many plant responses are at least in part also controlled at the level of protein turnover. It is a challenge for signal transduction research to understand how distinct incoming signals are integrated to generate specific changes at the transcript or protein level. The activity of luciferase (LUC) reporters can be detected in nondestructive qualitative and quantitative assays in vivo. Therefore, LUC reporters are particularly well suited for the detection of changes at the transcript and protein level. To the best of our knowledge, the number of plant transformation vectors for LUC fusions is very limited. In this article, we describe the LucTrap plant transformation vectors that allow generation of targeted and random transcriptional and translational fusions with the modified firefly LUC reporter LUC+. We demonstrate that LucTrap-based fusions can be used to monitor rapid changes in gene expression and protein abundance in vivo.
AB - Proper plant growth and development strongly rely on the plant's ability to respond dynamically to signals and cues from the intra- and extracellular environment. Whereas many of these responses require specific changes at the level of gene expression, in recent years it has become increasingly clear that many plant responses are at least in part also controlled at the level of protein turnover. It is a challenge for signal transduction research to understand how distinct incoming signals are integrated to generate specific changes at the transcript or protein level. The activity of luciferase (LUC) reporters can be detected in nondestructive qualitative and quantitative assays in vivo. Therefore, LUC reporters are particularly well suited for the detection of changes at the transcript and protein level. To the best of our knowledge, the number of plant transformation vectors for LUC fusions is very limited. In this article, we describe the LucTrap plant transformation vectors that allow generation of targeted and random transcriptional and translational fusions with the modified firefly LUC reporter LUC+. We demonstrate that LucTrap-based fusions can be used to monitor rapid changes in gene expression and protein abundance in vivo.
UR - http://www.scopus.com/inward/record.url?scp=33745453676&partnerID=8YFLogxK
U2 - 10.1104/pp.106.078097
DO - 10.1104/pp.106.078097
M3 - Article
C2 - 16684932
AN - SCOPUS:33745453676
SN - 0032-0889
VL - 141
SP - 3
EP - 14
JO - Plant Physiology
JF - Plant Physiology
IS - 1
ER -