AI Article Synopsis

  • Chlamydomonas reinhardtii, a biflagellate alga, has tightly regulated flagellar length, influenced by the LF1 gene, which is essential for normal flagella assembly.
  • A mutation in the LF1 gene leads to the production of extra-long flagella and slow regeneration after amputation due to a specific genetic change that creates a premature stop signal.
  • Molecular analysis via BAC libraries revealed that the LF1 protein, necessary for regulating flagellar length, primarily accumulates in the cell body rather than in the flagella, indicating that only a portion of the LF1 protein is needed for its function.

Article Abstract

Flagellar length is tightly regulated in the biflagellate alga Chlamydomonas reinhardtii. Several genes required for control of flagellar length have been identified, including LF1, a gene required to assemble normal-length flagella. The lf1 mutation causes cells to assemble extra-long flagella and to regenerate flagella very slowly after amputation. Here we describe the positional cloning and molecular characterization of the LF1 gene using a bacterial artificial chromosome (BAC) library. LF1 encodes a protein of 804 amino acids with no obvious sequence homologs in other organisms. The single LF1 mutant allele is caused by a transversion that produces an amber stop at codon 87. Rescue of the lf1 phenotype upon transformation was obtained with clones containing the complete LF1 gene as well as clones that lack the last two exons of the gene, indicating that only the amino-terminal portion of the LF1 gene product (LF1p) is required for function. Although LF1 helps regulate flagellar length, the LF1p localizes almost exclusively in the cell body, with <1% of total cellular LF1p localizing to the flagella.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1449559PMC
http://dx.doi.org/10.1534/genetics.104.027615DOI Listing

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