In vivo screening reveals interactions between Drosophila Manf and genes involved in the mitochondria and the ubiquinone synthesis pathway
© The Author(s). 2017
Received: 1 September 2016
Accepted: 8 May 2017
Published: 2 June 2017
Mesencephalic Astrocyte-derived Neurotrophic Factor (MANF) and Cerebral Dopamine Neurotrophic Factor (CDNF) form an evolutionarily conserved family of neurotrophic factors. Orthologues for MANF/CDNF are the only neurotrophic factors as yet identified in invertebrates with conserved amino acid sequence. Previous studies indicate that mammalian MANF and CDNF support and protect brain dopaminergic system in non-cell-autonomous manner. However, MANF has also been shown to function intracellularly in the endoplasmic reticulum. To date, the knowledge on the interacting partners of MANF/CDNF and signaling pathways they activate is rudimentary. Here, we have employed the Drosophila genetics to screen for potential interaction partners of Drosophila Manf (DmManf) in vivo.
We first show that DmManf plays a role in the development of Drosophila wing. We exploited this function by using Drosophila UAS-RNAi lines and discovered novel genetic interactions of DmManf with genes known to function in the mitochondria. We also found evidence of an interaction between DmManf and the Drosophila homologue encoding Ku70, the closest structural homologue of SAP domain of mammalian MANF.
In addition to the previously known functions of MANF/CDNF protein family, DmManf also interacts with mitochondria-related genes. Our data supports the functional importance of these evolutionarily significant proteins and provides new insights for the future studies.
KeywordsMANF CDNF Genetic screen Mitochondria Ubiquinone
An evolutionarily conserved protein family, MANF/CDNF family, is the most recently discovered family of neurotrophic factors (NTFs) [1–4]. Typically of NTFs, MANF and CDNF are small secreted molecules that support the survival of neurons [1, 2]. Mammalian MANF and CDNF support the brain dopaminergic system in rodent models of Parkinson’s disease (PD) in vivo [2, 5, 6]. MANF has been shown to protect neurons and cardiomyocytes against ischemic injury in extracellular manner [7, 8]. Additionally, MANF is required for the proliferation and survival of the pancreatic β-cells .
Orthologues for MANF/CDNF are the only neurotrophic factors as yet identified in invertebrates with conserved amino acid sequence [1, 3]. The invertebrate homologues show higher similarity to mammalian MANF than CDNF [2, 3]. However, both human MANF and CDNF are functional orthologues of Drosophila Manf (DmManf) [3, 10]. In Drosophila, glial-derived DmManf is necessary for maintaining the neurites of embryonic and larval dopaminergic neurons that do not express DmManf. This demonstrates that the extracellular trophic function for dopaminergic system is conserved .
The knowledge on the molecular interactions of MANF/CDNF family proteins remains limited. Also the receptor for MANF/CDNF proteins is not known. Intracellularly, mammalian MANF has been shown to bind GRP78/BiP (Glucose-regulated protein 78/Binding immunoglobulin protein), the major ER chaperone, in Ca2+-dependent manner . There is also experimental evidence suggesting that MANF interacts with KDEL-Rs, KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptors . Furthermore, a recent study suggests that MANF interacts with a member of ER-associated reticulon protein family . Our previous study shows a genetic interaction between DmManf and Drosophila homologues of GRP78, PERK (PRKR-like endoplasmic reticulum kinase, one of the ER stress sensor proteins) and Xbp1 (X-box Binding Protein-1, a transcription factor mainly mediating ER stress response activated gene expression) . Additionally, our earlier microarray analysis suggests that DmManf has a role in Drosophila ER stress response . MANF is localized to ER [14–17] and the retention is mediated through the non-classical but evolutionarily conserved ER retention signal sequence, RTDL in human and RSEL in Drosophila [8, 10, 17]. Furthermore, the expression of Manf mRNA is induced in response to ER stress [13, 15, 17–20]. In addition to GRP78, co-immunoprecipitation studies have revealed that MANF (also known as Armet) interacts with a mutant form of an extracellular matrix protein matrilin 3 .
Both mammalian and Drosophila MANF have been shown to hold intracellular cytoprotective function against Bax (BCL-2 associated X) -dependent cell death in vitro [10, 22]. The C-terminal domain of MANF shows high structural homology to SAP (SAF-A/B, Acinus and PIAS) domain of Ku70 (Ku autoantigen p70 subunit), an inhibitor of Bax-mediated apoptosis , and it is alone capable of protecting neurons from induced apoptosis in vitro [10, 22].
MANF and CDNF have been suggested to be involved in inflammatory responses [24–28]. The main mediator of proinflammatory response, NF-κB (nuclear factor kappa-light-chain-enhancer of activated B cells), is also regulated by unfolded protein response, a cellular process activated by ER stress (reviewed e.g. in ). In a recent study MANF was found to bind the p65 subunit of NF-κB via the C-terminal SAP-domain in vitro . Upon inflammation, MANF localized to nucleus and was suggested to suppress the expression of NF-κB targets by binding to DNA binding domain of p65 as well as to adjacent enhancer regions of target genes . Interestingly, recent study demonstrated that MANF has a conserved immune modulatory function in both Drosophila and mouse promoting tissue repair and regeneration in retina .
In this work we used RNA interference (RNAi) approach in UAS/GAL4 in vivo system to study interacting partners of DmManf in Drosophila model. In the binary UAS/GAL4 system, GAL4 lines with various expression patterns are used for tissue-specific expression of UAS (upstream activation sequence) -transgenes . RNAi where double stranded RNA (dsRNA) induces the degradation of targeted mRNA  is commonly used for gene silencing. Transgenic genome-wide Drosophila RNAi libraries have been established  (http://www.shigen.nig.ac.jp/fly/nigfly/) by introducing dsRNAs under UAS promotor. Crossing these flies with different GAL4 driver lines enables tissue-specific target gene inactivation. Expression of other UAS constructs or markers (e.g. GFP) can be simultaneously activated in the same GAL4 expression pattern. In this study, we used UAS-DmManf-RNAi construct for targeted knockdown of DmManf and performed a partial, unbiased screen of RNAi libraries in vivo to discover novel interacting partners for DmManf. Here we demonstrate genetic interactions between DmManf and genes with mitochondrial function.
Silencing of DmManf by UAS-DmManf-RNAi is effective and specific in vivo
Homozygous DmManf mutants die at early developmental stage . To study the role of DmManf during later stages of development we used the UAS/GAL4 system for tissue-specific knockdown of DmManf [31, 33]. Three UAS-DmManf-RNAi fly stocks were obtained from Vienna Drosophila RNAi Center (VDRC) (A in Additional file 1). All transformant lines showed similar phenotypes with different GAL4 drivers (B in Additional file 1), and the transformant line 12835 with construct ID 4793 was used in further experiments.
According to information provided by VDRC, there are no predicted off-targets for DmManf-RNAi construct ID 4793. To verify the specificity of DmManf-RNAi, DmManf was simultaneously overexpressed (by UAS-DmManf L3) and knocked down (by UAS-DmManf-RNAi) with ubiquitous tub-GAL4 driver. The overexpression of DmManf rescued the pupal lethality phenotype of ubiquitous DmManf knockdown flies into adulthood (Fig. 1a–b). We also used overexpression of the UAS constructs encoding transcripts for DmManf human (Hs) orthologues, HsMANF and HsCDNF, which share less homology with the DmManf-RNAi construct (C in Additional file 1) than DmManf. Both HsMANF and HsCDNF rescued the pupal lethality observed in DmManf ubiquitous knockdown flies (Fig. 1a–b). When two UAS constructs are used in the same fly, GAL4 protein supply is shared by the two promotor regions and might lead to decreased expression of UAS targets. In the case of UAS-RNAi lines, this dose effect could compromise the knockdown efficiency. To confirm that the rescue of DmManf knockdown phenotype was not due to inefficient knockdown of DmManf, we used UAS-DmManf-RNAi; UAS-mCD8-GFP line as a dose control for UAS/GAL4 binary expression system. Ubiquitous knockdown of DmManf by UAS-DmManf-RNAi; UAS-mCD8-GFP with tub-GAL4 showed similar proportion of expected pupae to UAS-DmManf-RNAi alone (Fig. 1a–b).
Wing-specific knockdown of DmManf drastically alters wing morphology and increases cell proliferation
DmManf is ubiquitously expressed in 3rd instar larval wing disc . To verify the efficiency of tissue-specific silencing of DmManf, we used salm-GAL4 and en-GAL4 to knock down DmManf and simultaneously express UAS-mCD8-GFP to visualize the GAL4 expression pattern in the larval wing disc. The loss of DmManf immunoreactivity was detected exactly according to salm-GAL4 and en-GAL4 expression pattern in the wing disc (Fig. 1e) further demonstrating that the knockdown of DmManf was efficient at protein level. Interestingly, in DmManf knockdown wing discs we detected mild but clear increase of DmManf immunoreactivity in regions next to the GAL4 expressing area (Fig. 1e). This might indicate a compensatory regulation of DmManf expression in response to the partial loss of DmManf in the wing disc.
Penetrance of the wing phenotype in adult flies of DmManf knockdown with MS1096-GAL4
Proportion of males with phenotype
Proportion of females with phenotype
Simultaneous expression of UAS-DmManf L3 and UAS-DmManf-RNAi with MS1096-GAL4 returned the wings back to wild type (c1-c2 in Fig. 2a) indicating that overexpression of DmManf could rescue the wing phenotype. Co-expression of UAS-HsMANF or UAS-HsCDNF together with UAS-DmManf-RNAi by MS1096-GAL4 also rescued the wing phenotype (d1-d4 and e1-e4 in Fig. 2a). This further demonstrated that the knockdown of DmManf by UAS-DmManf-RNAi construct was specific to the DmManf mRNA only and suggests that DmManf plays an important role during wing development.
Screening of DmManf interaction partners
The putative interactions between DmManf and the 21 candidate genes were further analysed by ubiquitous knockdown of the candidate genes (stage 4 in Additional file 2, B-C in Additional file 3, Additional file 4). We used tub-GAL4 driver and compared pupal and adult viability between wild type background and with DmManf overexpression to see whether overexpression of DmManf would affect the phenotypes caused by ubiquitous knockdown of the candidate genes. For example, simultaneous overexpression of DmManf significantly decreased the pupal viability for ubiquitous knockdown of CSN3 (COP9 complex homolog subunit 3) encoding a protein involved in regulation of the ubiquitin conjugation pathway (B-C in Additional file 3). Overexpression of DmManf alone with tub-GAL4 in wild type background showed no obvious phenotype or affected fly viability .
Gene ontology terms of potential DmManf interacting partners
Enrichment of Drosophila GO terms in the partial RNAi screen
ubiquinone metabolic process
oxidoreduction coenzyme metabolic process
quinone cofactor metabolic process
COQ7, ND75, Tom20, CG6455
COQ7, ND75, Tom20, CG6455
COQ7, Hsp68, Aats-phe, ND75, Tom20, CG6455
COQ7, ND75, Tom20, CG6455
COQ7, ND75, Tom20, CG6455
cellular metabolic process
betaTry, COQ7, dome, Hsp68, Ku70/Irbp, ND75, Aats-phe, pABp, Spn27A, Taf5, Ts, Cdk12/CG7597, COQ3/CG9249
COQ7, ND75, Tom20, CG6455
DmManf partially localizes to mitochondria and genetically interacts with the ubiquinone synthesis pathway
To examine further the interaction between DmManf and genes encoding mitochondrial proteins, we studied the subcellular localization of DmManf. According to our previous analyses, DmManf is localized to several cell compartments . To detect mitochondria, we used sqh-EYFP-Mito transgenic fly line . When the CNS of 3rd instar sqh-EYFP-Mito larvae were immunohistochemically stained with DmManf antibody, a partial co-localization with mitochondrial marker was detected (Fig. 5c and Additional file 5).
Video of 3D volume rendering of co-localization of a-DmManf and sqh-EYFP-Mito. A mov file. DmManf expression (magenta) adjoined the sqh-EYFP-Mito marker (green). (MOV 6408 kb)
Knockdown of COQ3/CG9249 with 69B-GAL4 and tub-GAL4 led to lethality at pupal and larval stages, respectively, and was not affected by either heterozygous DmManf Δ96 mutant background or overexpression of DmManf (Fig. 4 and Additional file 4). When COQ3/CG9249 was knocked down with MS1096-GAL4 in wild type background, a bent-up phenotype was observed in the adult wing (b1 and b3 in Fig. 5a, a1 and a3 in Fig. 5b). This phenotype was stronger leading to wrinkled wings when either simultaneous overexpression of DmManf (b1-b4 in Fig. 5a) or heterozygous DmManf Δ96 mutant background (a1-a4 in Fig. 5b) was used. Ubiquitous knockdown of COQ3/CG9249 with tub-GAL4 showed a very slight increase in DmManf mRNA levels detected by qPCR analysis (Fig. 6a).
In Drosophila, only six genes are annotated to be involved in processes related to the ubiquinone synthesis pathway (GO:0006744 term in FlyBase, http://flybase.org; Fig. 6b). We decided to study interaction between DmManf and the rest of the ubiquinone synthesis pathway genes, COQ2/CG9613, COQ6/CG7277, COQ9/CG30493, and COQ4/CG32174 (Fig. 6b–c). Wing-specific knockdown of any of these genes with MS1096-GAL4 showed no phenotype (Fig. 6c). Knockdown with semi-ubiquitous 69B-GAL4 driver showed either no phenotype (in the case of COQ6 and COQ4) or led to lethality at pupal stage (COQ9 and COQ2) and observed phenotype was not altered by either heterozygous DmManf Δ96 mutant background or simultaneous overexpression of DmManf (Fig. 6c). Simultaneous overexpression of DmManf did not affect the observed phenotype by ubiquitous knockdown of COQ6, COQ9 and COQ4 with tub-GAL4. However, we observed significantly decreased pupal viability when COQ2 was ubiquitously knocked down by tub-GAL4 in DmManf-overexpressing background compared to the wild type background (B in Additional file 3; Additional file 4).
DmManf genetically interacts with Irbp, the Drosophila homologue of Ku70
We noted that Irbp knockdown with MS1096-GAL4 resulted in smaller wing discs of 3rd instar wandering larvae in comparison to wild type (Fig. 7b). We quantified the width of the wing disc above the wing pouch area (indicated by red dashed line in Fig. 7b) and found that in the Irbp knockdown flies the width of the wing disc was significantly decreased in comparison to wild type (Fig. 7c). We also studied whether the heterozygous DmManf mutant background would affect the width of the wing disc in Irbp knockdown larvae with MS1096-GAL4 and thus explain the altered wing phenotype of Irbp knockdown flies in this background. However, there was no difference in the width of the wing disc when Irbp was knocked down in wild type and heterozygous DmManf mutant backgrounds (Fig. 7c).
We observed lethality at pupal stage when Irbp was ubiquitously knocked down with tub-GAL4 (B in Additional file 3). Simultaneous overexpression of DmManf partially rescued this lethality to adulthood (B-C in Additional file 3) suggesting that DmManf and Irbp may act in the same pathway and have, to certain extent, redundant function.
To examine whether altered expression level of Irbp and DmManf affect each other, we collected embryos of DmManf knockdown as well as wandering 3rd instar larvae of Irbp knockdown and DmManf overexpression with semi-ubiquitous 69B-GAL driver and quantified Irbp and DmManf mRNA levels by qPCR analysis. In DmManf knockdown embryos, DmManf mRNA expression level was significantly decreased in comparison to the control (Fig. 7d). Interestingly, Irbp mRNA expression was also significantly decreased in DmManf knockdown embryos (Fig. 7d) indicating that loss of DmManf downregulated Irbp expression.
In Irbp knockdown larvae Irbp mRNA level was significantly decreased while DmManf mRNA expression was not altered (Fig. 7e). In DmManf-overexpressing larvae, the level of Irbp mRNA did not differ from the control genotype (Fig. 7e). When Irbp knockdown was done in wild type and DmManf-overexpressing backgrounds, the decreased Irbp mRNA level was not affected (Fig. 7e) indicating that the overexpression of DmManf does not neither induce nor repress Irbp mRNA expression. We also studied the effect of Irbp knockdown on DmManf protein expression by investigating wing discs of Irbp knockdown 3rd instar larvae. In line with our qPCR analysis, DmManf immunoreactivity was not altered in Irbp knockdown with MS1096-GAL4 in comparison to wild type (Fig. 7b).
Based on the structural homology between the Bax-inhibiting SAP domain of Ku70 and C-terminal domain of MANF [22, 23], we hypothesized that the total loss of DmManf in vivo could lead to decreased inhibition of Bax followed by increased cell death and subsequent DmManf Δ96 mutant lethality. Thus, we tested whether the loss of Debcl (death executioner Bcl-2 homologue), a homologue to mammalian proapoptotic Bax subfamily, could rescue the DmManf Δ96 mutant lethality in vivo. We used two debcl mutant alleles (loss-of-function allele debcl E26 and putative dominant negative allele debcl W105 ) to abolish endogenous Debcl  and UAS-debcl-RNAi line together with ubiquitous da-GAL4 driver to knock down Debcl. However, neither the loss nor silencing of Debcl could rescue the DmManf Δ96 mutant lethality (Additional file 6) suggesting that during development DmManf action through other molecular systems than Debcl is more crucial for viability.
MANF and CDNF form an evolutionarily conserved family of neurotrophic factors [1–3]. Since their discovery, increasing data suggests that these proteins possess other characteristics beyond their neurotrophic properties. The loss of Drosophila homologue, DmManf, results in lethality at early developmental stages with neuronal and cuticular defects . Thus, we wanted to explore the tissue-specific effects of knockdown of DmManf using UAS-RNAi approach. In a previous study, neither neuronal nor glial knockdown of DmManf showed any obvious phenotypic effects without the overexpression of Dicer-2, a component of RNAi machinery . Here, we demonstrated that knockdown of DmManf by UAS-DmManf-RNAi construct is effective and specific. The ubiquitous knockdown resembled the lethal phenotype of homozygous DmManf Δ96 mutants. We detected a phenotype in the wing when knocking down DmManf with a wing-specific driver MS1096-GAL4. The wing phenotype was stronger in heterozygous DmManf Δ96 mutant background as compared to the wild type background further demonstrating the specificity of UAS-DmManf-RNAi construct. Although the phenotype of small or even absent wings observed in the DmManf knockdown adult males would suggest a decrease in cell number, the number of mitotic cells was significantly increased in the wing disc of DmManf knockdown larvae. Our results are in accordance with the previous study showing that the silencing of human MANF in HeLa cells stimulated cell proliferation . The increased appearance of the mitotic markers used in this study could also be due to prolonged M phase of cell cycle. This would be in line with our finding that the density of cells was not altered between wild type and DmManf knockdown larval wing discs (data not shown). Prolonged cell cycle would result in decreased growth rate and could explain the wing phenotype observed in DmManf knockdown flies. Furthermore, we failed to detect any differences with apoptotic markers (data not shown) indicating that the wing phenotype did not result from increased cell death at the 3rd instar larval stage. However, it is possible that apoptosis could take place later at the pupal stage.
The knowledge on the molecular mechanisms and signaling pathways of MANF/CDNF family proteins is still limited. Previous studies show strong evidence supporting MANF function in ER stress and unfolded protein response [8, 9, 15, 17, 20]. In our recent study, we showed that the expression of DmManf mRNA is upregulated in response to ER stress-inducing drugs and that DmManf genetically interacts with genes known to function in ER stress and unfolded protein response . In the current work we utilized the wing phenotype detected in DmManf knockdown flies and performed a partial unbiased screen of two genome-wide UAS-RNAi libraries using the Drosophila in vivo model. The primary screen was done with wing-specific driver (MS1096-GAL4) and the selection of candidate genes was based solely on phenotypic similarity to DmManf-knockdown flies. We were unable to find genes with ER- and ER stress-related functions as potential interaction partners for DmManf because of this criterion: knockdown of ER stress related genes with MS1096-GAL4 driver resulted in distinct phenotypes in comparison to the knockdown of DmManf . In the secondary and tertiary screens we knocked down the candidate genes in (1) heterozygous DmManf Δ96 mutant background to decrease the level of endogenous DmManf protein and (2) with simultaneous overexpression of DmManf to increase it . Thus, we aimed to discover whether the phenotype caused by silencing of a particular gene would be affected by manipulating DmManf expression level.
Although our screen was only partial, it strongly suggested that DmManf interacts with genes encoding mitochondrial proteins. Mitochondria play crucial roles e.g. in oxidative phosphorylation and Ca2+ signaling, and their dysfunctional biogenesis and metabolism are involved in a variety of human diseases (reviewed in [46–48]). We found that DmManf partially co-localized with the mitochondrial marker sqh-EYFP-Mito. Deeper analysis revealed that strongest DmManf expression was detected adjoining the mitochondrial marker. In sqh-EYFP-Mito marker, the fluorophore is directed to mitochondria by the signal peptide of human Cox8A (cytochrome C oxidase subunit 8A) and localized to the mitochondrial matrix . Since DmManf is also localized to ER [10, 14], the observed co-localization could be on the membranes connecting ER and mitochondria. DmManf could take part in the ER-mitochondrial crosstalk and disturbances in DmManf protein levels could affect protein transport to mitochondria. A specific complex, TOM (translocase of outer membrane), is needed for proper targeting of mitochondrial proteins encoded by nuclear DNA (reviewed in ). We identified genetic interaction between DmManf and Tom20 (Translocase of the outer membrane 20, homologue to human TOMM20 and TOMM20-L), a receptor subunit of TOM. Interestingly, another receptor protein of TOM, Maggie/TOMM22 has been shown to mediate localization of pro-apoptotic Debcl (homologue of mammalian Bax) to mitochondria in Drosophila . Bax, together with other members of the Bcl-2 protein family, regulates permeabilization of mitochondrial outer membrane during apoptosis (reviewed in ). Previous studies have revealed a role for MANF in Bax-induced cell death in vitro [10, 22]. In addition, our screen data suggests a genetic interaction between MANF and Ku70/Irbp, an inhibitor of Bax/Debcl. In future, it would be interesting to evaluate whether DmManf co-localizes with TOM proteins and whether Irbp or Debcl have any role in this interaction.
Two genes from the ubiquinone synthesis pathway, COQ7 and CG9249/COQ3, were included in our primary screen and identified as candidate interacting partners of DmManf. We also found evidence for interaction between DmManf and a third component of ubiquinone synthesis pathway, CG9613/COQ2. The knockdown of COQ7 or CG9249/COQ3 resulted in elevated DmManf mRNA levels. The best known function of ubiquinone, also known as coenzyme Q (Q), is its participation in electron transport chain (ETC) by transferring electrons from complexes I and II to complex III (reviewed in [42, 43, 52]). COQ7 hydroxylates demethoxyubiquinone (DMQ) into hydroxyquinone  from which ubiquinone is formed by COQ3 . Loss of COQ7 (also known as Mclk-1 in mice, clk-1 in nematodes) leads to Q deficiency and impaired ATP synthesis [55–58]. Q deficiency in humans (OMIM 607426) is associated with variety of clinical manifestations, mostly neuronal and muscular defects (reviewed e.g. in ). Importantly, increasing evidence suggests that mitochondrial dysfunction is one of the main causes of PD (reviewed e.g. in ) and studies on neuroprotection by Q treatment in PD models have been promising (reviewed in ). Q deficiency has been linked to destabilization of mitochondrial complex I . Complex I is also associated with PD as mutations in its subunits are found to be involved in a familial form of PD (OMIM 556500; reviewed in ). Furthermore, toxins used to induce PD-like symptoms in animal models include MPTP, rotenone and paraquat which all interfere with complex I functionality [62, 63]. In addition to genes involved in Q synthesis, we found homologues for two genes linked to human mitochondrial complex I deficiency (OMIM 252010), ND75 (NDUFS1) and l(2)37Bb (FOXRED1) to genetically interact with DmManf. Considering all our data indicating a mitochondrial function, DmManf could affect the oxidative phosphorylation, directly or indirectly. In future studies, the connection between DmManf protein and its function in mitochondria should be thoroughly examined.
Alternatively, DmManf could play a role in maintaining cellular Ca2+ homeostasis, an important function of both mitochondria and ER, based on Ca2+-dependent binding of mammalian MANF and GRP78 . In our previous study, cultured Schneider 2 -cells showed a strong induction of DmManf mRNA expression in response to thapsigargin, an inhibitor of ER membrane-resident Ca2+ ATPase, which depletes Ca2+ from ER . Additionally, one of our candidate genes, CG6455, is homologous to human IMMT (inner membrane protein, mitochondrial) predicted with a function in mitochondrial Ca2+ homeostasis.
For several of our candidate genes, e.g. CG9249/COQ3, knockdown with MS1096-GAL4 in both DmManf Δ96 heterozygous mutant (with decreased DmManf protein level) and overexpression (with increased DmManf protein level) background resulted in more severe phenotype in comparison to the phenotype observed in wild type background. This suggests that knockdown of certain genes together with the imbalance of DmManf protein level affects overall cellular homeostasis rather than disturbs a putative stoichiometric relationship between DmManf and candidate gene encoded protein levels. Furthermore, while the genetic interaction discovered may represent a physical or biochemical interaction, it might also indicate a secondary effect resulting from involvement of DmManf and candidate gene in the same signaling pathway or biological process.
This study revealed that DmManf is involved in Drosophila wing development and expanded our knowledge on the role of MANF in the maintenance of cellular homeostasis. Importantly, we discovered novel genetic interacting partners of DmManf and our study suggests that MANF has a role in mitochondrial function. These data help us understand the molecular mechanism of the evolutionarily conserved MANF/CDNF protein family in future studies.
Fly strains and antibodies
Fly stocks and crosses were maintained at 25 °C. The following fly lines were used in the study: w −, UAS-DmManf 133 (line L3), UAS-DmManf 135 (line L5) and DmManf Δ96 /TM6 Tb Sb EYFP , UAS-HsMANF L2 and UAS-HsCDNF L1 , UAS-lacZ . The following lines were obtained from Bloomington Drosophila Stock Center: 69B-GAL4 (#1774, ), A9-GAL4 (#8761, ), da-GAL4 (#5460, ), en2.4-GAL4e16E (#30564, A. Brand & K. Yoffe, unpublished), MS1096-GAL4 (#8860, ), salm-GAL4 (#5818, ), Ser-GAL4 (#6791, ), tub-GAL4/TM6 Tb Sb EYFP (#5138) and UAS-mCD8-GFP (#5130) , debcl E26 (#27342) and debcl W105 /CyO (#27341) , act-His2Av-mRFP (#23651, ), UAS-GFP.nls (#4775, ) and sqh-EYFP-Mito (#7194, ). UAS-S/G2/M-Green was obtained from Kyoto Stock Center (#109676, ). Combination of act-His2Av-mRFP and UAS-S/G2/M-Green in 2nd chromosome was a kind gift from Jinghua Gui. T(2;3)SM6a-TM6B Tb translocation balancer was used in viability studies (referred as SM6-TM6). UAS-RNAi lines were obtained from Vienna Drosophila RNAi Center and National Institute of Genetics (Additional file 7). Adult flies were imaged with ProgRes SpeedXT camera (Jenoptik). The following antibodies were used: rabbit anti-DmManf , rabbit anti-phospho-Histone H3 (Ser10) (06–570, Upstate), anti-α-tubulin (DM1A, Sigma).
Immunohistochemistry, confocal microscopy and image analysis
Third instar larval wing discs and CNS were dissected in PBS and fixed with 4% paraformaldehyde in PBS or PEM (100 mM PIPES pH 7.0, 2 mM EGTA, 1 mM MgSO4) for 30 min. Fixed tissues were washed with PBT (0.1% Triton X-100 in PBS) and blocked with blocking solution (1% BSA in PBT) for 1 h. Tissues were incubated with primary antibody overnight at 4 °C and with secondary antibody for 1 h in room temperature, and mounted in VECTASHIELD® Mounting Medium (Vector Laboratories). Samples were imaged with TCS SP5 laser scanning microscope (Leica Microsystems) equipped with HCX PL APO 20×/0.7 mm Imm Corr glycerol immersion objective or HC PL APO 10×/0.4 air objective. For co-localization study, Zeiss LSM5 DUO confocal microscope equipped with PL APO 100×/1.4 oil objective was used. ImageJ 1.43u , Imaris 7.6.0 and Imaris 8.4.1 (Bitplane Inc.) were used for image analysis. For quantification of pHis3 positive cells, automatic “Spots” algorithm in Imaris 7.6.0 was used. For quantification of S/G2/M-Green and act-His2Av-RFP positive cells, a 37.9 μm × 37.9 μm area of the dorsal wing pouch was analyzed with the Spots algorithm in Imaris 8.4.1.
Western blot analysis
Lysis buffer (20 mM Tris-HCl pH 7.4, 150 mM NaCl, 1% Triton X-100, 1 mM EDTA) supplemented with Complete proteinase inhibitor tablets (Roche) was used in homogenization of larvae. Western blotting was done according to manufacturer’s instructions and visualized by the Odyssey infrared imager (Li-Cor).
Adult wing preparations
Adult flies were dipped into 70% ethanol and fixed 10 min in clove oil (Sigma). Wings were dissected and mounted in 70% Canada Balsam/30% xylene. Nikon SMZ1500 was used for imaging.
Larvae were grown at 25 °C on apple juice plates and collected 50–54 h after egg laying. For 3rd instar larval samples wandering larvae were collected from the vials. Embryos were collected from apple juice plates 16–22 h after egg laying. NucleoSpin® RNA II (Macherey-Nagel) was used in extraction and purification of total RNA. DNase treatment was done on-column according to the manufacturer’s instructions. First strand cDNA was synthesized from total RNA (1 μg) using RevertAid Premium Reverse Transcriptase (Thermo Scientific) and Oligo(dT18) primer at 53 °C according to manufacturer’s instructions. Expression of DmManf mRNA was quantified by LightCycler® 480 Real-Time PCR System with Lightcycler 480 SYBR Green I master mix (Roche) with primers DmManf forward 5′-AATCTGCGACCTTCGCTATG-3’and DmManf reverse 5′-TCGTTGAGGATTTTCTTCAGG-3′ . Irbp was amplified with primers Irbp forward 5′-AGTTCATCACGTTGTCAAGAGC-3′ and Irbp reverse 5′-TACGATCGGACAGGATTTCG-3′ . RpL32 was amplified as a reference gene with primers RpL32 forward 5′-CGGATCGATATGCTAAGCTGT-3′ and RpL32 reverse 5′-GCGCTTGTTCGATCCGTA-3′ . PCR efficiency (E) of each primer pair was determined from a relative standard curve. For DmManf, E = 1.98; for Irbp, E = 2.00; for RpL32, E = 1.97. Equation E-Cp in which Cp indicates a crossing point was used to calculate relative concentration of DmManf, Irbp and RpL32 mRNA in each sample. To present the results, the concentration of DmManf and Irbp was normalized to the level of RpL32. Each sample was analysed as a duplicate.
Means were compared by Student’s t-test, null hypothesis was rejected at P < 0.05. Statistical analyses were performed by using Microsoft® Excel Analysis ToolPak (Microsoft® Office Professional Plus 2010). For pupal viability studies, normal (Tubby+; Tb+) and squat (Tb−) pupae were counted, the number of Tb+ pupae was divided by the number of all pupae and normalized to experimentally determined ratio from tub-GAL4/TM6 Tb Sb cross to wild type and to wild type balanced against SM6-TM6 translocation balancer (Additional file 4 and Additional file 8, wild type and DmManf overexpression data previously reported in ). For preliminary analyses two vials were counted and statistical analysis was done based on six vials with minimum of 40 pupae. For genotypes showing incomplete penetrance of the wing phenotypes, quantification of the penetrance was performed by counting adult flies with and without phenotype from 4 vials per genotype.
Gene ontology analysis
Gene Ontology (GO) analysis was performed for genes considered as hits from our UAS-RNAi screen (21 genes) against the set of genes included in the primary screen (approximately 2800 randomly selected genes). GOstat (http://gostat.wehi.edu.au/) was used with default tool settings. A complete list of overrepresented (p < 0.1) GO terms is presented in Table 2.
We are grateful to Evely Vridolin and Osamu Shimmi for performing the majority of the primary screening of UAS-RNAi lines and sharing the results with us. Arja Ikävalko and Sari Tynkkynen are acknowledged for their excellent technical assistance and Zeng Zhao and Lin Feng for help with primary screening. We thank Jukka Kallijärvi and Osamu Shimmi for critical reading of the manuscript and Ville Hietakangas, Shinya Matsuda, Mika Molin and Jaana Vulli for invaluable advice. We thank Bloomington Drosophila Stock Center, Vienna Drosophila RNAi Center, Kyoto Stock Center, National Institute of Genetics (Japan), Osamu Shimmi, Ville Hietakangas and Jinghua Gui for fly stocks, and Juha Partanen for sharing antibodies. Confocal imaging was performed at the Light Microscopy Unit, Institute of Biotechnology.
RL was supported by Viikki Doctoral Programme in Molecular Biosciences, The Finnish Parkinson Foundation, The Ella and Georg Ehrnrooth Foundation, The University of Helsinki Funds, and Alfred Kordelin Foundation. PL was supported by The Academy of Finland (grant No. 139910). MP was supported by Estonian Research Council (grant No. IUT19–18). TIH was supported by Helsinki University Funds.
Availability of data and materials
All data generated or analysed during this study are included in this published article and its additional files.
RL and TIH designed the research, RL with the help of MP and TIH performed the genetic crosses, immunohistochemistry, microscopy and image analysis, PL performed qPCR and Western blot analyses, RL analysed the data and wrote the draft manuscript. All authors read, made corrections and approved the manuscript.
The authors declare that they have no competing interests.
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