The publisher would like to apologise on behalf of the authors. Since publication of:
The Serotonin Transporter Expression in Drosophila melanogaster
Thomas Giang1, Steffen Rauchfuss2, Maite Ogueta3 and Henrike Scholz1
1Department of Animal Physiology, University of Cologne, Köln, Germany
2Julius-Maximilians-University of Würzburg, Institute of Genetics and Neurobiology,Würzburg, Germany
3Departmento Biología Celular y Patología, Instituto de Neurociencias de Castilla y León, Salamanca, Spain
in the Journal of Neurogenetics, Volume 25: Pages 17–26, the authors have informed us of the following insertions and correction:
Author list:
Thomas Giang1*, Yvonne Ritze2,3*, Steffen Rauchfuss2, Maite Ogueta2,4 and Henrike Scholz1,2
1Department of Animal Physiology, University of Cologne, Köln, Germany
2Julius-Maximilians-University of Würzburg, Institute of Genetics and Neurobiology, Würzburg, Germany
3Current address: Department of Nutritional Medicine, University of Hohenheim, Stuttgart, Germany
4Current address: Departmento Biología Celular y Patología, Instituto de Neurociencias de Castilla y León, Salamanca, Spain
*These authors contributed equally to the present work
Author contributions:
TG and HS developed the concept for the paper and wrote the manuscript, with the description of dSERT antibody generation and text for provided by YR. YR generated dSERT fusion protein as antigen and performed initial characterizations with MO of the antisera and serotonin labeling in the larval brain and in the adult brain. The data (2A) was generated by YR and Anne Haberberger which we like to thank here. TG collected data and designed figure 1, 2, 4C and 4D, 5. SR collected data for figure 3. MO developed the concept generated the data and designed figure 4A and 4B. The initial observation that there are local differences of dSERT and 5HT was made by MO. YR generated data and designed . HS generated data and designed figure 7 (was 6).
Insertion in Methods section:
Generation of antisera
A 392 base pair fragment of the dsert cDNA (RE10485) starting from the N-terminus with no homologies to other transporters from Drosophila or other species (between the nucleotide + 4586 to + 4978 relative to the transcription start side) was amplified using the linker primers AAA GAA TTC AAA TGG ACC GCA GCG GG and TTT CTC GAG CTC CGC CTT CTG TCC (EcoRI- and XhoI-linkers are underlined). The fragment was cloned directionally into the pGEX expression vector (GE Healthcare Life Science, USA). The 46 kDa GST fusion protein was purified with sepharose beads according to the manufacturer's instructions (Sigma-Aldrich, Germany) and used to immunize rabbits (Eurogenetec). The polyclonal antiserum was tested for specificity for the SERT fusion protein with western blot analysis and used at a concentration of 1:1500 – 2000 for immunohistochemistry.
Insertion in Results section after headline “dSERT Expression in Serotonergic Neurons”
The distribution of dSERT protein was also examined with the dSERT antiserum in sections of adult fly brain and co-localized with the staining of an antibody against 5-HT (). All cell bodies that expressed dSERT were positive for 5-HT and vice versa. Examples of specific 5HT expressing cell body clusters – specifically LP1, LP2, SP1, SP2 and SE3 - that express dSERT are shown at higher magnification (a-d’’). In addition, overlapping expression of 5-HT and dSERT was found in projections and dot-like varicosities throughout the brain (’’, B’’). For example partial overlap of dSERT and 5-HT expression was found in the central complex. In the ellipsoid body dSERT and 5-HT staining was co-localized in the outer ring and less pronounced in the inner or middle ring (’, A’’). In the fan-shaped body, 5-HT and dSERT immunoreactive staining was mainly found in a glomerular-like pattern in the outer layers (’, A’’).
Insertion of new :
Renaming of as Figure 7 (including all references to it).