Envelope-to: rd120@XXXX Delivery-date: Fri, 5 Mar 2004 17:08:57 \+0000 Mime-Version: 1.0 X-Sender: ysharma@XXXX Date: Fri, 5 Mar 2004 12:08:02 \-0500 To: rd120@XXXX From: Yashoda Sharma <ysharma@XXXX> Subject: Flybase update X-Cam-ScannerInfo: http://www.cam.ac.uk/cs/email/scanner/ X-Cam-AntiVirus: No virus found X-Cam-SpamDetails: scanned, SpamAssassin (score=0.2, MIME_MISSING_BOUNDARY 0.16) Hello Rachel, About a year ago you contacted me about CG15148, which I asked you to rename Dhc36D, due to its sequence properties. I am writing to give you an update of this gene. My thesis work at the University of Iowa, with Dr. Daniel Eberl has revealed that Dhc36D is the previously identified audition gene beethoven. I've attached a synopsis of my findings. We would appreciate it very much if you could include this as a communication to FlyBase and update the information. If you have any questions please contact me at this email. Please let me know the status of this. thank you for your assistance in this matter Yashoda PCR, Southern analysis, and sequencing data indicate that the audition gene, beethoven (btv) is encoded by the Drosophila DHC1b isoform, Dhc36D. As the 1b isoform, btv appears to serve as the retrograde motor for intraflagellar transport specifically in the sensory cilia of Johnston's organ. This finding is supported by EM studies that show that the Johnston's organ cilia are disrupted (Eberl et al., 1997), similarly to DHC1b mutant cilia from other organisms, especially those of C. elegans (Signor et al., 1999). The defective btv cilia resemble those in mutants for the other recently identified Drosophila IFT components (Han et al., 2003; Sarpal et al., 2003). btv mutants are fertile, confirming the findings of Han and Sarpal that IFT is not required for Drosophila sperm development. The lesion in the btv5P1 allele (EMS-induced) is a 401 basepair deletion and a 6 basepair insertion. This likely eliminates one of the P-loop motifs required for ATP hydrolysis, or it may result in the production of a truncated protein. The other btv allele, k07109b is likely a 'hit and run' lesion, which we have not yet defined molecularly, but is NOT associated with the k07109b insertion of the PlacW element, which is actually present in the FasIII gene nearby.