Vkuehn Week 11

Journal Club Preparation: Leishmania Major

Genome Reference Paper: The Genome of the Kinetoplastid Parasite, Leishmania major (Reference Genome)

Article Outline

Introduction

• It is important to study the genome of Leishmania major because of the various human diseases that this parasite is capable of causing. If infected by a leishmania parasite a number of diseases can form. Annually there are 2 million cases in 88 tropical and subtropical countries.
• How it infects:
  1. Parasite transmitted by sand flies as proliferative promastigote
  2. Differentiate into nondividing forms before inoculation into vertebrate host
  3. In host macrophages, phagocytose metacyclics --> differentiate into amastigotes (proliferate in phagolysosome)
  4. Leads to host macrophage lysis and infection of other macrophages
  5. Outcome of infection depends on species, host immune system and host genetics
• Interesting to look at genome because of the unique mechanism of regulating transcription which is atypical for eukaryotes

  Leishmania major is considered an "Old World Leishmania" species, meaning it contains 36 chromosome pairs. There are approximately 30 Leishmania species who's gene order is highly conserved.

  Ways in which it differs:

  1. Organization of protein coding genes: long, strand-specific polycistronic clusters
  2. No transcription factors

• This article determined the genome sequence of Leishmania major on a chromosome by chromosome basis. Present the structure and content based on molecular processes such as:
  • chromatin remodeling
  • transcription
  • RNA processing
  • Translation
  • posttranslational modification
  • protein turnover

  Also discuss essential host parasite interface developmental processes

Genome Structure and Content

• 32,816,678 base pairs obtained by shotgun sequencing insert colonies and purified chromosomal DNA
• Genome is partially aneuploid
• L. major sequence analysis yielded 911 RNA genes, 39 pseudogenes, 8272 protein coding genes
• L. major telomeres distinct from other Trityps and have heterogeneous structure
• The end of Leishmania major chromosomes have tripartite "repeat-repeat" structure
• "Leichmania restricted" genes: responsible for metablic differences from T. brucei and T. cruzi found randomly distributed in genome
• Two genes of interest: LmjF33.1740 and LmjF33.1750
  • Because resulting proteins contain macrophage migration inhibition factor (MIF)
  • Homologues found in other Leishmania species
  • L. major MIFs thought to retain tautomerase activity, but dies not have oxidoreductase activity.

    Interesting because this ties it to eukaryotic similarities but also ties genes to bacteria

  • Suggests that L. major MIFs could use eukaryotic similarities to modulate host macrophage response and help them survive in the host

RNA Genes

• RNAs participate in many cellular processes:

  RNA replication, splicing, RNA processing and modification, translation, translation regulation, protein translocation across membranes

• Differences in organization of RNA genes in genomes of L. major and the other trypanosomes.

  All 3 tritryp genomes have different numbers of genes and location differs as well.

Chromatin Remodeling

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