Abstract
The PRDM family transcription repressor Blimp‐1 is present in almost all multicellular organisms and plays important roles in various developmental processes. This factor has several conserved motifs among different species, but the function of each motif is unclear. Drosophila Blimp‐1 plays an important role in determining pupation timing by acting as an unstable transcriptional repressor of the βftz‐f1 gene. Thus, Drosophila provides a good system for analyzing the molecular and biological functions of each region in Blimp‐1. Various Blimp‐1 mutants carrying deletions at the conserved motifs were induced under the control of the heat shock promoter in prepupae, and the expression patterns of βFTZ‐F1 and Blimp‐1 and pupation timing were observed. The results showed that the regions with strong and weak repressor functions exist within the proline‐rich middle section of the factor and near the N‐terminal conserved motif, respectively. Rapid degradation was supported by multiple regions that were mainly located in a large proline‐rich region. Results revealed that pupation timing was affected by the repression ability and stability of Blimp‐1. This suggests that both the repression function and instability of Blimp‐1 are indispensable for the precise determination of pupation timing.
Transcriptional repressor Blimp‐1 in Drosophila rapidly degrades, and this is important in determining of pupation timing. Expressed Blimp‐1 disappears slowly depending on the position of deletion in the factor. This indicates that the factor degrades through multiple target sites in the factor for the rapid degradation.