Summary of Study ST002571
This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001658. The data can be accessed directly via it's Project DOI: 10.21228/M8CX2C This work is supported by NIH grant, U2C- DK119886.
See: https://www.metabolomicsworkbench.org/about/howtocite.php
This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.
Study ID | ST002571 |
Study Title | Quantification of cytokinins in ap1 cal AP1-GR and drmy1 ap1 cal AP1-GR inflorescences using LC-MS |
Study Type | Quantification using mass spectrometry |
Study Summary | Robustness is the invariant development of phenotype despite environmental changes and genetic perturbations. In the Arabidopsis flower bud, four sepals initiate at robust positions and times and grow to equal size to enclose and protect the inner floral organs. We previously characterized the mutant development related myb-like1 (drmy1), where 3-5 sepals initiate at irregular positions and variable times and grow to different sizes, compromising their protective function. This loss of robustness was caused by a uniform increase in cytokinin signaling, as revealed by the TCS::GFP reporter, in the floral meristem before sepal initiation. We hypothesized that the increase in cytokinin signaling in drmy1 was due to an increase in the level of cytokinins. To test this idea, we extracted cytokinins from induced inflorescences of wild-type (5 bio-reps) and drmy1 (6 bio-reps) in ap1 cal AP1-GR background. We measured the level of three cytokinin bases, trans-Zeatin (tZ), cis-Zeatin (cZ), and isopentenyladenine (iP), and their corresponding nucleosides (tZR, cZR, and iPR), using liquid chromatography-mass spectrometry. We found that there was no statistically significant differences in cytokinin levels between these genotypes, indicating that the increase in cytokinin signaling in the drmy1 floral meristem is not due to increased cytokinin levels. |
Institute | Cornell University |
Department | Plant Biology Section |
Laboratory | Roeder Lab |
Last Name | Kong |
First Name | Shuyao |
Address | 239 Weill Hall, 526 Campus Road, Ithaca, NY 14853 |
sk3245@cornell.edu | |
Phone | 6072629684 |
Submit Date | 2023-04-20 |
Num Groups | 2 |
Total Subjects | 11 |
Raw Data Available | Yes |
Raw Data File Type(s) | raw(Thermo) |
Analysis Type Detail | LC-MS |
Release Date | 2023-05-11 |
Release Version | 1 |
Select appropriate tab below to view additional metadata details:
Combined analysis:
Analysis ID | AN004236 |
---|---|
Analysis type | MS |
Chromatography type | Reversed phase |
Chromatography system | Waters Acquity |
Column | Waters ACQUITY UPLC BEH C18 (100 x 2.1mm,1.7um) |
MS Type | ESI |
MS instrument type | Orbitrap |
MS instrument name | Thermo Q Exactive HF hybrid Orbitrap |
Ion Mode | POSITIVE |
Units | Peak area |
Chromatography:
Chromatography ID: | CH003143 |
Chromatography Summary: | 1 µl of each sample was injected into a Thermo Fisher Scientific Vanquish Horizon UHPLC System coupled with a Thermo Q Exactive HF hybrid quadropole-orbitrap high-resolution mass spectrometer equipped with a HESI ion source. Samples were separated on a C18 ODS column (AQUITY UPLC BEH C18, 1.7 μm, 2.1 × 100 mm, Waters), at a flow rate of 0.3 ml/min, with linear gradients of solvent A (0.1% formic acid) and solvent B (0.1% formic acid in methanol) according to the following profile: 0 min, 99.0% A + 1.0% B; 4.0 min, 55.0% A + 45.0% B; 7 min, 30.0% A + 70.0% B; and then with isocratic conditions: 8 min, 1.0% A + 99.0% B; 12 min, 99.0% A + 1.0% B. |
Methods Filename: | Protocol_SK.PDF |
Instrument Name: | Waters Acquity |
Column Name: | Waters ACQUITY UPLC BEH C18 (100 x 2.1mm,1.7um) |
Column Temperature: | 60 °C |
Flow Gradient: | 0 min, 99.0% A + 1.0% B; 4.0 min, 55.0% A + 45.0% B; 7 min, 30.0% A + 70.0% B; and then with isocratic conditions: 8 min, 1.0% A + 99.0% B; 12 min, 99.0% A + 1.0% B |
Flow Rate: | 0.3 ml/min |
Internal Standard: | BAP |
Solvent A: | 100% water; 0.1% formic acid |
Solvent B: | 100% methanol; 0.1% formic acid |
Preconditioning: | Mili-Q H2O |
Chromatography Type: | Reversed phase |