FB2026_03 , released September 17, 2026
Reference Report
Open Close
Reference
Citation
Fasulo, B. (1999.9.15). EDRC99 - abstract ID298. 
FlyBase ID
FBrf0111606
Publication Type
Personal communication to FlyBase
Abstract
PubMed ID
PubMed Central ID
Text of Personal Communication
Subject: EDRC99 - abstract ID298
Dear Dr. Fasulo,
We are currently curating the abstracts for the upcoming European
Drosophila Research Conference in Zurich, for FlyBase. I am writing in
connection with your abstract:
'doppio fuso (duo), a gene required for spindle pole assembly during
Drosophila male meiosis'
You mention a gene that is new to FlyBase, duo.
Do you have a map location for duo? It is nice if we can keep as many
gene records as possible anchored to the map.
Also, you state that the P-element causing the duo mutation 'lies in
the 5' untranslated region of a gene that encodes a poly-A-binding
protein'.
FlyBase has a record of 3 genes encoding a poly-A-binding protein.
These are 'pAbp' (at 55B), 'Rox2' (also known as 'polyA-binding protein
II', at 44B), 'Rox8' (at 95D). Is the duo mutation in one of these 3
genes, or is it in a new poly-A-binding protein ?
Thank you for your help,
with best wishes,
Chihiro
\----------------------------------------------------------------------
Chihiro Yamada.
FlyBase (Cambridge),
\----------------------------------------------------------------------
Dear Dr. Yamada,
thanks for giving me the possibility to clarify my assertions:
\- duo is the mutant's name. It describes the cytological phenotype of a
polyA-binding protein allele.
\- by in situ ibridization we have positioned the P insertion at 55B.
Thank you,
with best wishes,
Barbara
Barbara Fasulo
Dipartimento di Genetica e Biologia Molecolare
Universita' di Roma 'La Sapienza'
Ple Aldo Moro 5
Roma 00185
ITALY
DOI
Associated Information
Comments
Associated Files
Other Information
Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Abbreviation
    Title
    ISBN/ISSN
    Data From Reference
    Alleles (1)
    Genes (1)