4.5 Article

Role of p38 in replication of Trypanosoma brucei kinetoplast DNA

Journal

MOLECULAR AND CELLULAR BIOLOGY
Volume 26, Issue 14, Pages 5382-5393

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/mcb.00369-06

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Funding

  1. NIAID NIH HHS [AI058613, R01 AI058613] Funding Source: Medline
  2. NIGMS NIH HHS [GM31819, R01 GM031819] Funding Source: Medline

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Trypanosomes have an unusual mitochondrial genome, called kinetoplast DNA, that is a giant network containing thousands of interlocked minicircles. During kinetoplast DNA synthesis, minicircles are released from the network for replication as 6-structures, and then the free minicircle progeny reattach to the network. We report that a mitochondrial protein, which we term p38, functions in kinetoplast DNA replication. RNA interference (RNAi) of p38 resulted in loss of kinetoplast DNA and accumulation of a novel free minicircle species named fraction S. Fraction S minicircles are so underwound that on isolation they become highly negatively supertwisted and develop a region of Z-DNA. p38 binds to minicircle sequences within the replication origin. We conclude that cells with RNAi-induced loss of p38 cannot initiate minicircle replication, although they can extensively unwind free minicircles.

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