A new name for the oviraptorid dinosaur "Ingenia" yanshini (Barsbold, 1981; preoccupied by Gerlach, 1957).

The genus name of the small oviraptorid dinosaur Ingenia yanshini is preoccupied by the tripyloidid nematode Ingenia mirabilis, thus making the former a junior homonym of the latter.  Although "Ingenia" yanshini is sympatric with Conchoraptor gracilis, it is distinguished from Conchoraptor by proportions of the manus.  It also differs appreciably from the ingeniines Heyuannia huangi and Nemegtomaia barsboldi in manual and pelvic proportions.

The trans-acting flagellar regulatory proteins, FliX and FlbD, play a central role in linking flagellar biogenesis and cytokinesis in Caulobacter crescentus.

The FliX/FlbD-dependent temporal transcription of late flagellar genes in Caulobacter crescentus requires the assembly of an early, class II-encoded flagellar structure. Class II flagellar-mutant strains exhibit a delay in the completion of cell division, with the accumulation of filamentous cells in culture. It is shown here that this cell-division defect is attributable to an arrest in the final stages of cell separation.

The conserved flaF gene has a critical role in coupling flagellin translation and assembly in Caulobacter crescentus.

The expression of the flagellin proteins in Caulobacter crescentus is regulated by the progression of flagellar assembly both at the transcriptional and post-transcriptional levels. An early basal body structure is required for the transcription of flagellin genes, whereas the ensuing assembly of a hook structure is required for flagellin protein synthesis. Previous experiments have shown that the negative regulatory protein, FlbT, operates this second post-transcriptional checkpoint by associating with the 5' untranslated region (UTR) of the fljK flagellin transcript, inhibiting translation and destabilizing the mRNA.

Productive interaction between the chromosome partitioning proteins, ParA and ParB, is required for the progression of the cell cycle in Caulobacter crescentus.

In Caulobacter crescentus the partitioning proteins ParA and ParB operate a molecular switch that couples chromosome partitioning to cytokinesis. Homologues of these proteins have been shown to be important for the stable inheritance of F-plasmids and the prophage form of bacteriophage P1. In C.

ParB-stimulated nucleotide exchange regulates a switch in functionally distinct ParA activities.

ParA and ParB of Caulobacter crescentus belong to a conserved family of bacterial proteins implicated in chromosome segregation. ParB binds to DNA sequences adjacent to the origin of replication and localizes to opposite cell poles shortly following the initiation of DNA replication. ParA has homology to a conserved and widespread family of ATPases.