The zinc finger protein ZAT11 modulates paraquat-induced programmed cell death in Arabidopsis thaliana

2013 ◽  
Vol 35 (6) ◽  
pp. 1863-1871 ◽  
Author(s):  
Muhammad Kamran Qureshi ◽  
Neerakkal Sujeeth ◽  
Tsanko S. Gechev ◽  
Jacques Hille
Keyword(s):  
Arabidopsis Thaliana ◽  
Cell Death ◽  
Programmed Cell Death ◽  
Zinc Finger ◽  
Zinc Finger Protein ◽  
Finger Protein

Zinc finger protein RP-8, the Bombyx mori ortholog of programmed cell death 2, regulates cell proliferation

2020 ◽  
Vol 104 ◽  
pp. 103542 ◽  
Author(s):  
Muhammad Nadeem Abbas ◽  
Hanghua Liang ◽  
Saima Kausar ◽  
Zhen Dong ◽  
Hongjuan Cui
Keyword(s):  
Cell Proliferation ◽  
Cell Death ◽  
Programmed Cell Death ◽  
Bombyx Mori ◽  
Zinc Finger ◽  
Zinc Finger Protein ◽  
Finger Protein

scholarly journals Requirement for the Murine Zinc Finger Protein ZFR in Perigastrulation Growth and Survival

2001 ◽  
Vol 21 (8) ◽  
pp. 2880-2890 ◽  
Author(s):  
Madeleine J. Meagher ◽  
Robert E. Braun
Keyword(s):  
Cell Death ◽  
Programmed Cell Death ◽  
Zinc Finger ◽  
Zinc Finger Protein ◽  
Cellular Growth ◽  
Gene Encoding ◽  
Growth And Survival ◽  
Finger Protein ◽  
Development Delay ◽  
Cellular Phenotypes

ABSTRACT The transition from preimplantation to postimplantation development leads to the initiation of complex cellular differentiation and morphogenetic movements, a dramatic decrease in cell cycle length, and a commensurate increase in the size of the embryo. Accompanying these changes is the need for the transfer of nutrients from the mother to the embryo and the elaboration of sophisticated genetic networks that monitor genomic integrity and the homeostatic control of cellular growth, differentiation, and programmed cell death. To determine the function of the murine zinc finger protein ZFR in these events, we generated mice carrying a null mutation in the gene encoding it. Homozygous mutant embryos form normal-appearing blastocysts that implant and initiate the process of gastrulation. Mutant embryos form mesoderm but they are delayed in their development and fail to form normal anterior embryonic structures. Loss of ZFR function leads to both an increase in programmed cell death and a decrease in mitotic index, especially in the region of the distal tip of the embryonic ectoderm. Mutant embryos also have an apparent reduction in apical vacuoles in the columnar visceral endoderm cells in the extraembryonic region. Together, these cellular phenotypes lead to a dramatic development delay and embryonic death by 8 to 9 days of gestation, which are independent of p53 function.

scholarly journals DPL-1 DP, LIN-35 Rb and EFL-1 E2F Act With the MCD-1 Zinc-Finger Protein to Promote Programmed Cell Death in Caenorhabditis elegans

Genetics ◽  
2007 ◽  
Vol 175 (4) ◽  
pp. 1719-1733 ◽  
Author(s):  
Peter W. Reddien ◽  
Erik C. Andersen ◽  
Michael C. Huang ◽  
H. Robert Horvitz
Keyword(s):  
Cell Death ◽  
Caenorhabditis Elegans ◽  
Programmed Cell Death ◽  
Zinc Finger ◽  
Zinc Finger Protein ◽  
Finger Protein

The CCCH zinc finger protein gene AtZFP1 improves salt resistance in Arabidopsis thaliana

2014 ◽  
Vol 86 (3) ◽  
pp. 237-253 ◽  
Author(s):  
Guoliang Han ◽  
Mingjie Wang ◽  
Fang Yuan ◽  
Na Sui ◽  
Jie Song ◽  
...  
Keyword(s):  
Arabidopsis Thaliana ◽  
Zinc Finger ◽  
Protein Gene ◽  
Zinc Finger Protein ◽  
Salt Resistance ◽  
Zinc Finger Protein Gene ◽  
Ccch Zinc Finger ◽  
Finger Protein

scholarly journals Expression of Zinc Finger Protein Zat12 from Arabidopsis thaliana in Escherichia coli

2020 ◽  
Vol 3 (1) ◽  
pp. 504-511
Author(s):  
Le Thi Tuyet Cham ◽  
Vu Ngoc Thang ◽  
Tran Anh Tuan ◽  
Vu Thi Thuy Hang
Keyword(s):  
Arabidopsis Thaliana ◽  
Zinc Finger ◽  
Stress Responses ◽  
Zinc Finger Protein ◽  
Expression System ◽  
Direct Interaction ◽  
Early Response ◽  
In Planta ◽  
Abiotic Stress Response ◽  
Finger Protein

The C2H2 zinc finger protein ZAT12 has been classified as a plant core abiotic stress response gene in the early  response to multiple stresses. ZAT12 links the iron deficiency and oxidative stress responses through the direct interaction with/and negative regulation of a central regulator - FIT. For further research on the regulation of the ZAT12 protein in planta, a huge quantity of ZAT12 proteins is required to inject into mice for the generation of ZAT12 antiserum. In this study, the gene encoding the ZAT12 protein from Arabidopsis thaliana was cloned into the expression vector - pETBlue-2 and then overexpressed in E. coli T7. A high expression level was indicated by SDS-PAGE. Immunoblot demonstrated successful expression using a bacterial expression system.

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