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Missense mutation of a class B heat shock factor is responsible for the tomato bushy root-2 phenotype

Molecular Horticulture 2022年第1期2卷 51-62页

作者： Zoltan Kevei Silva Demetryus Silva Ferreira Cristina Maria Perez Casenave Tomasz Kurowski Fady Mohareb Daniel Rickett chris stain Andrew J.Thompson Cranfield Soil and AgriFood Institute College RoadCranfield UniversityBedfordshire MK430ALUK Syngenta Crop Protection Jealott’s Hill International Research CentreBracknellBerkshire RG426EYUK

The bushy root-2(brt-2)tomato mutant has twisting roots,and slower plant *** we used whole genome resequencing and genetic mapping to show that brt-2 is caused by a serine to cysteine(S75C)substitution in the DNA binding domain(DBD)of a heat shock factor class B(HsfB)encoded by *** gene is orthologous to the Arabidopsis SCHIZORIZA gene,also known as *** brt-2 phenotype is very similar to Arabidopsis lines in which the function of AtHsfB4 is altered:a proliferation of lateral root cap and root meristematic tissues,and a tendency for lateral root cap cells to easily *** brt-2 S75C mutation is unusual because all other reported amino acid substitutions in the highly conserved DBD of eukaryotic heat shock factors are dominant negative mutations,but brt-2 is *** further show through reciprocal grafting that brt-2 exerts its effects predominantly through the root genotype even through BRT-2 is expressed at similar levels in both root and shoot *** AtHsfB4 is induced by root knot nematodes(RKN),and loss-of-function mutants of this gene are resistant to RKNs,BRT-2 could be a target gene for RKN resistance,an important trait in tomato rootstock ***&accession numbers SolycHsfB4a-Solyc04g078770.

关键词： Bushy root-2 Genetic mapping HsfB4 Root knot nematode resistance SCHIZORIZA Tomato

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Intracellular in situ labeling of Ti02 nanoparticles for fluorescence microscopy detection

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Nano Research 2018年第1期11卷 464-476页

作者： Koshonna Brown Ted Thurn Lun Xin William Liu Remon Bazak Si Chen Barry Lai Stefan Vogt chris Jacobsen Tatjana Paunesku Gayle E. Woloschak Department of Radiation Oncology Feinberg School of Medicine Northwestern University Chicago Illinois 60611 USA X-ray Science Division Advanced Photon Source Argonne National Laboratory 9700 South Cass Avenue Argonne Illinois 60439 USA Department of Physics & Astronomy Weinberg College of Arts and Sciences 2145 Sheridan Road Evanston Illinois 60208 USA

Titanium dioxide （TiO2） nanoparticles are produced for many different purposes, including development of therapeutic and diagnostic nanoparticles for cancer detection and treatment, drug delivery, induction of DNA double-strand breaks, and imaging of specific cells and subcellular structures. Currently, the use of optical microscopy, an imaging technique most accessible to biology and medical patholog36 to detect TiO2 nanoparticles in cells and tissues ex vivo is limited with low detection limits, while more sensitive imaging methods （transmission electron microscopy, X-ray fluorescence microscop~ etc.） have low throughput and technical and operational complications. Herein, we describe two in situ post- treatment labeling approaches to stain TiO2 nanoparticles taken up by the cells. The first approach utilizes fluorescent biotin and fluorescent streptavidin to label the nanoparticles before and after cellular uptake; the second approach is based on the copper-catalyzed azide-alkyne cycloaddition, the so-called Click chemistry, for labeling and detection of azide-conjugated TiO2 nanoparticles with alkyne- conjugated fluorescent dyes such as Alexa Fluor 488. To confirm that optical fluorescence signals of these nanoparticles match the distribution of the Ti element, we used synchrotron X-ray fluorescence microscopy （XFM） at the Advanced Photon Source at Argonne National Laboratory. Titanium-specific XFM showed excellent overlap with the location of optical fluorescence detected by confocal microscopy. Therefore, future experiments with TiO2 nanoparticles may safely rely on confocal microscopy after in situ nanoparticle labeling using approaches described here.

关键词： TiO2 nanoparticles anatase Click reaction biotin-streptavidin synchrotron X-ray fluorescence microscopy

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