AI Article Synopsis

  • The first isolation of a cDNA clone for a functional DNA helicase from pea (Pisum sativum) reveals it to be part of the DEAD-box protein family, unique for its substitution of motifs.
  • The isolated 45.5 kDa protein exhibits various activities, including ATP-dependent helicase functions, and shows a strong similarity to eIF-4A, previously not associated with DNA helicase.
  • This enzyme, expressed in different pea organs and located in the nucleus and cytosol, plays a significant role in cellular processes by unwinding DNA and enhancing topoisomerase I activity.

Article Abstract

DNA helicases play an essential role in all aspects of nucleic acid metabolism, by providing a duplex-unwinding function. This is the first report of the isolation of a cDNA (1.6 kb) clone encoding functional DNA helicase from a plant (pea, Pisum sativum). The deduced amino-acid sequence has eight conserved helicase motifs of the DEAD-box protein family. It is a unique member of this family, containing DESD and SRT motifs instead of DEAD/H and SAT. The encoded 45.5 kDa protein has been overexpressed in bacteria and purified to homogeneity. The purified protein contains ATP-dependent DNA and RNA helicase, DNA-dependent ATPase, and ATP-binding activities. The protein sequence contains striking homology with eIF-4A, which has not so far been reported as DNA helicase. The antibodies against pea helicase inhibit in vitro translation. The gene is expressed as 1.6 kb mRNA in different organs of pea. The enzyme is localized in the nucleus and cytosol, and unwinds DNA in the 3' to 5' direction. The pea helicase interacts with pea topoisomerase I protein and stimulates its activity. These results suggest that pea DNA helicase could be an important multifunctional protein involved in protein synthesis, maintaining the basic activities of the cell, and in upregulation of topoisomerase I activity. The discovery of such a protein with intrinsic multiple activity should make an important contribution to our better understanding of DNA and RNA transactions in plants.

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http://dx.doi.org/10.1046/j.1365-313x.2000.00869.xDOI Listing

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