HOMOLOGOUS STRAND EXCHANGE AND DNA HELICASE ACTIVITIES IN PLANT MITOCHONDRIA by
نویسندگان
چکیده
HOMOLOGOUS STRAND EXCHANGE AND DNA HELICASE ACTIVITIES IN PLANT MITOCHONDRIA Daqing Song Department of Microbiology & Molecular Biology Master of Science Homologous recombination is critical for generating genetic variation in living organisms by exchange and rearrangement of DNA. Most of our knowledge about homologous recombination is limited to processes in bacteria or in eukaryotic nuclei. In E. coli, homologous recombination is dependent on the RecA protein. Higher plant chloroplasts have RecA-like strand exchange activity. However, little is known about these mechanisms in higher plant mitochondria. I have detected a RecA-like strand exchange activity in soybean mitochondria. This activity forms joint molecules in the presence of ATP, Mg, and homologous DNA substrates. In addition, the E. coli single-stranded DNA binding (SSB) protein is a non-sequence-specific DNA binding protein that functions as an accessory factor for RecA protein-promoted strand exchange reactions. Our lab has identified an Arabidopsis homologue of E. coli SSB that is targeted to mitochondria (mtSSB). The results of my research shows the mtSSB protein has the same properties as the E. coli SSB protein and it can stimulate the E. coli RecA protein-promoted strand exchange reactions. DNA helicases utilize the energy of ATP to separate the two parental DNA strands at the replicating fork or during recombinational strand exchange. Although higher plant chloroplast helicase activity has been reported, no such activity has heretofore been identified in higher plant mitochondria. We report the characterization of a plant mitochondrial DNA helicase isolated from soybean leaves. ATP is required for this enzyme and this enzyme poorly utilizes any other NTPs or dNTPs. The enzyme requires Mg for activity. This enzyme only has 3’ to 5’unwinding activity. The optimal conditions for mitochondrial DNA helicase are 2 mM ATP, 8 to 10 mM Mg, 100 to 200 mM NaCl and 37-42 C incubation for one hour or longer time.
منابع مشابه
Homologous DNA strand exchange activity of the human mitochondrial DNA helicase TWINKLE
A crucial component of the human mitochondrial DNA replisome is the ring-shaped helicase TWINKLE-a phage T7-gene 4-like protein expressed in the nucleus and localized in the human mitochondria. Our previous studies showed that despite being a helicase, TWINKLE has unique DNA annealing activity. At the time, the implications of DNA annealing by TWINKLE were unclear. Herein, we report that TWINKL...
متن کاملIn vitro strand exchange promoted by the herpes simplex virus type-1 single strand DNA-binding protein (ICP8) and DNA helicase-primase.
The genome of herpes simplex virus type-1 undergoes a high frequency of homologous recombination in the absence of a virus-encoded RecA-type protein. We hypothesized that viral homologous recombination is mediated by the combined action of the viral single strand DNA-binding protein (ICP8) and helicase-primase. Our results show that ICP8 catalyzes the formation of recombination intermediates (j...
متن کاملPhage T4 homologous strand exchange: A DNA helicase, not the strand transferase, drives polar branch migration
Homologous strand exchange is a central step in general genetic recombination. A multiprotein complex composed of five purified bacteriophage T4 proteins (the products of the uvsX, uvsY, 32, 41, and 59 genes) that mediates strand exchange under physiologically relevant conditions has been reconstituted. One of these proteins, the product of the uvsY gene, is required for homologous pairing but ...
متن کاملHuman DNA Helicase B Functions in Cellular Homologous Recombination and Stimulates Rad51-Mediated 5′-3′ Heteroduplex Extension In Vitro
Homologous recombination is involved in the repair of DNA damage and collapsed replication fork, and is critical for the maintenance of genomic stability. Its process involves a network of proteins with different enzymatic activities. Human DNA helicase B (HDHB) is a robust 5'-3' DNA helicase which accumulates on chromatin in cells exposed to DNA damage. HDHB facilitates cellular recovery from ...
متن کاملContext-dependent remodeling of Rad51-DNA complexes by Srs2 is mediated by a specific protein-protein interaction.
The yeast Srs2 helicase removes Rad51 nucleoprotein filaments from single-stranded DNA (ssDNA), preventing DNA strand invasion and exchange by homologous recombination. This activity requires a physical interaction between Srs2 and Rad51, which stimulates ATP turnover in the Rad51 nucleoprotein filament and causes dissociation of Rad51 from ssDNA. Srs2 also possesses a DNA unwinding activity an...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2005