Somatostatin-IRES-Cre Mice: Between Knockout and Wild-Type?

The neuropeptide somatostatin (SOM) is widely expressed in rodent brain and somatostatin-IRES-Cre (SOM-cre) mouse strains are increasingly used to unravel the physiology of SOM-containing neurons. However, while knock-in targeting strategy greatly improves Cre-Lox system accuracy, recent reports have shown that genomic insertion of Cre construct per se can markedly affect physiological function. We show that Cre transgene insertion into the 3′UTR of the somatostatin gene leads to the selective and massive depletion of endogenous SOM in all tested brain regions. It also strongly impacts SOM-related neuroendocrine responses in a similar manner to what has been reported for SST KO mice: increased corticosterone levels after 30-min restraint stress, decreased amplitude and regularity of ultradian growth hormone secretory patterns accompanied by changes in sexually dimorphic liver gene expression (serpina1, Cyp2b9, Cyp2a4, Cyp2d9, and Cyp7b1). In addition to demonstrating the need for examination of the consequences of Cre transgenesis, these results also reveal how this SOM-cre strain may be a useful tool in studying the functional consequences of moderate to low SOM levels as reported in neurological and psychiatric disorders.

The neuropeptide somatostatin (SOM) is widely expressed in rodent brain and somatostatin-IRES-Cre (SOM-cre) mouse strains are increasingly used to unravel the physiology of SOM-containing neurons. However, while knock-in targeting strategy greatly improves Cre-Lox system accuracy, recent reports have shown that genomic insertion of Cre construct per se can markedly affect physiological function. We show that Cre transgene insertion into the 3′UTR of the somatostatin gene leads to the selective and massive depletion of endogenous SOM in all tested brain regions. It also strongly impacts SOM-related neuroendocrine responses in a similar manner to what has been reported for SST KO mice: increased corticosterone levels after 30-min restraint stress, decreased amplitude and regularity of ultradian growth hormone secretory patterns accompanied by changes in sexually dimorphic liver gene expression (serpina1, Cyp2b9, Cyp2a4, Cyp2d9, and Cyp7b1). In addition to demonstrating the need for examination of the consequences of Cre transgenesis, these results also reveal how this SOM-cre strain may be a useful tool in studying the functional consequences of moderate to low SOM levels as reported in neurological and psychiatric disorders.
Keywords: cre mice, corticosterone, growth hormone secretory patterns, hepatic expression, feminization inTrODUcTiOn The neuropeptide somatostatin (SOM, encoded by the sst gene) is largely expressed in mouse brain (1). In many regions, such as the cortex or hippocampus, it is co-expressed with gammaaminobutyric acid (GABA) and calretinin with the noticeable exception of the olfactory bulb where one-half of SOM-imunoreactive (SOM-ir) GABAergic neurons are parvalbumin-ir (PV-ir) (2). Transgenic somatostatin-Cre (SOM-Cre) mouse strains are increasingly used to unravel the physiological roles of somatostatin-containing neurons in the brain (3,4). However, while the knock-in targeting strategy greatly improved Cre-Lox system accuracy, genomic insertion of Cre constructs per se can markedly affect physiological function, depending on the genomic organization of the targeted gene. In SOM-IRES-Cre mouse line [Sst tm2.1(cre)Zjh /J mice (4)], the Cre construct was targeted to the 3′UTR region of the sst gene. In this study, we characterized the molecular and physiological impact of Cre transgene insertion on the endogenous SOM tone and SOM-related responses and show an allele-dependent impairment. The massive SOM loss observed in homozygous SOM-Cre mice was associated with exacerbated corticosterone responses, feminized growth hormone (GH) secretion, and GH-dependent hepatic gene expression profiles similar to previous reports for SST KO mice. The demonstration that SOM peptide levels and SOM-related physiological responses can be strongly impacted in homozygous SOM-Cre mice needs to be taken into account when using this SOM-Cre strain.

MaTerials anD MeThODs
Mice SOM-IRES-Cre mice [or SST-IRES-Cre, Sst tm2.1(cre)Zjh /J strain, # SN13044, Jackson Lab, Bar Harbor] and SST knockout mice (5) were bred in our animal facility on a 12 h light/dark cycle with ad libitum access to food and water. Three-to five-monthold wild-type (WT), heterozygous, and homozygous transgenic littermates were obtained from heterozygous breeding pairs. All procedures were approved by a local ethics committee (French MESR Authorization No. 00618.04) in accordance with the European Communities Council Directive (86/609/EU).

Quantitative rT-Pcr
Freshly dissected brain regions and liver samples from SOM-Cre or SST KO mice were frozen and kept at −80°C until use. Each sample was harvested in Trizol buffer (Trizol, Life Technologies) using cold Tissue Lyzer (Qiagen) and RNA were extracted using classical phenol-chloroform protocol. 500 ng total RNA was reverse transcribed using the High Capacity cDNA Reverse Transcription Kit (Applied, Life Technologies). Real-time quantitative PCR was performed with 10 ng cDNA using an automatized 1536-well qPCR plate preparation program (BRAVO, Agilent) coupled to LightCycler PCR System (Roche, Basel), allowing simultaneous amplification for several target genes in triplicate samples. Taqman

Biochemical assays
Mouse brain samples were homogenized by sonication in 2M acetic acid. After centrifugation, supernatants were lyophilized and stored at −80°C until use. SOM levels were determined by radioimmunoassay as previously described [sensitivity threshold 0.5 pg/tube (7)], or using a commercial EIA (Phoenix Pharmaceuticals). NPY levels were determined using a commercial RIA kit (Phoenix Pharmaceuticals). Intra-and inter-assay coefficients of variation were below 10%. Data were analyzed using ANOVA with Bonferroni post hoc test (Statview).
immunohistochemistry Deeply anesthetized SOM-Cre mice (WT and Tg/Tg littermates) were transcardially perfused with 4% paraformaldehyde (PFA). The brain was quickly removed, post-fixed 1 h in 4% PFA, cryoprotected, and then frozen in cold isopentane. 40 μm-thick coronal sections were cut with a freezing cryotome (Leica). Sections were rinsed in tris-buffered saline (TBS) and incubated in 10% normal donkey serum/0.3% Triton X100 TBS/0.05% sodium azide for 30 min, then incubated for 48 h in the same buffer with goat anti-SOM primary antibody (# D20, Santa Cruz Biotechnology, 1/1000). After several TBS rinses, sections were incubated for 2 h with A488-conjugated donkey anti-goat antibody (Invitrogen, 1/500 in TBS). After rinsing, sections were mounted on slides and coverslipped with fluoromount. Images from brain structures of WT and Tg/Tg mice were obtained under fluorescent illumination with identical settings on an AxioPlan microscope (Leica) equipped with MetaView imaging software.

acute restraint stress response
Isolated male mice were submitted to a 30 min restraint stress in a 50 ml Falcon tube with a ventilation hole. 4 µl of blood was sampled from the tail immediately before (basal) or 30 min after stress (stressed). Corticosterone (CORT) blood levels were assayed using RIA kits (Phoenix Pharmaceuticals). Data were analyzed using ANOVA with Bonferroni post hoc test and Wilcoxon nonparametric test (Statview).

assessment of Pulsatile gh secretion
In order to minimize stress, mice were acclimated to handling and blood sample collection for at least 2 weeks prior to the assessment of GH release. Ultradian variations of GH secretion were assessed as previously described (8,9). Briefly, sequential tail-tip blood samples (2 μl/sample from the same tail wound for the duration of the procedure) were collected every 10 min over a 6 h sampling period (0900-1500 hours) in freely behaving animals. Blood samples were collected and homogenized in 58 µl PBS 1×-0.05% tween on 96-well plates kept on ice, then transferred to −20°C for storage. GH concentrations were determined using an in-house mouse GH ELISA as previously described (10) and plotted as a function of time (8,9). Cumulative distributions of relative frequencies were analyzed using the two-sample Kolmogorov-Smirnov test (Prism, GraphPad Inc.).

Behavioral Testing
Mice were individually housed a week before the tests.

Open field
Each mouse was placed in a corner of a 50 cm × 50 cm × 45 cm square open field and its activity was recorded during 20 min in the peripheral (10 cm wide) or central (30 cm wide) zones. Global activity as well as distance and time spent in the central zone were quantified using Videotrack Software.

Forced-Swim Test
Each mouse was placed in a beaker filled with water (23°C) for 6 min. The sessions were recorded using Videotrack Software and the time spent swimming, climbing, or staying immobile during the session was analyzed a posteriori by a trained experimenter unaware of genotype.
Data were analyzed using ANOVA and Bonferroni post hoc test, using repeated measures for open field activity (Statview). Figure 1A, somatostatin expression (SST) was strongly reduced in the cortex of heterozygous and homozygous SOM-Cre mice for both sexes (genotype effect, P < 0.0001, male P < 0.0001, female P < 0.01) as compared to WT. Heterozygous (0/Tg) transgenic mice showed a 51 and 34% decrease in males and females, respectively, as compared to WT. Homozygous (Tg/Tg) transgenic mice showed an even greater decrease: 89% for males, and 86% for females. In contrast, CST, NPY (Figure 1A), and SSTR1-4 ( Figure 1B) mRNA levels were not significantly different in transgenic and control animals. Decreased SST expression was also detected in the hypothalamus in SOM-Cre mice (0/Tg: 50%, males and 58%, females; Tg/Tg: 92%, males and 87%, females), the hippocampus (0/Tg: 49%, males and 36%, females; Tg/Tg: 90%, males and 91%, females), or the olfactory bulb (0/Tg: 42%, males and 48%, females; Tg/Tg: 89%, males and 100%, females), three regions with highly differing SOM expression levels in the WT mice (data not shown). Except SST, no major changes in expression were found for the other markers (listed in Section "Materials and Methods") tested in heterozygous or homozygous SOM-Cre mice (data not shown).

As shown in
Somatostatin concentration (SOM) was measured in the cortex of WT, 0/Tg, and Tg/Tg SOM-Cre male mice. A 30% decrease was found in 0/Tg mice and SOM levels fell to 70% of WT in Tg/Tg mice ( Figure 1C) while NPY levels did not change. A massive decrease of SOM peptide levels in Tg/Tg mice was also detected in the hypothalamus, cerebellum, and olfactory bulb (70-90% decrease), while SST KO mice (SST −/− ) were used as negative controls (SOM-Cre vs WT, P < 0.0001; SST KO vs WT, P < 0.0001; hypothalamus vs all other regions, P < 0.0001; Figure 1D).
As shown on Figure 2, both cellular and fiber somatostatin labeling was strongly affected in SOM-Cre Tg/Tg brain, in cortex, hippocampus, hypothalamus (with a striking decrease of the staining in the median eminence), olfactory bulb, and amygdala (Figures 2A-E).
Since sexually dimorphism is highly dependent on GH secretion, GH secretory pulses were assayed during six consecutive hours in SOM-Cre WT and Tg/Tg males and females. Figure 4B illustrates mean GH secretion profiles and shows that typical male secretory profiles are no longer observed in SOM-Cre Tg/Tg males, as previously reported in SST KO males (11). SOM-Cre Tg/ Tg male profiles rather show a feminized pattern (i.e., secretory peaks are more frequent and of less amplitude), similar to the one observed in WT and Tg/Tg females (Figure 4B). Analysis of the cumulative frequency distributions (Figure 4C

DiscUssiOn
The application of Cre-based transgenic models using promoterdriven expression of Cre recombinase greatly improved our knowledge of anatomical connections and permitted the physiological dissection of cellular properties in neural circuitry (14,15). Crossing such models with mice expressing floxed fluorescent reporter proteins or gene-regulatory sequences allows for detection, targeting of genetic addition-or inactivation of a given gene [see Ref. (16) for review]. Several pitfalls have yet emerged, calling for the careful evaluation of appropriate controls prior to drawing metabolic or physiological conclusions (14,17). According to the spatial or temporal activation profile of the promoter used, it is recommended to carefully compare the distribution of promoterdriven Cre with the endogenous expression profile of the targeted gene. In particular, transient ontogenic expression of target genes can lead to permanent changes revealed at later stages as offtarget effects (18).
The initial stage of Cre transgene insertion per se must also be cautiously considered when using Cre-based technology since it can impact the function of this region. The commonly used transgenic strain SST-IRES-Cre line studied here was generated by insertion of IRES-Cre sequence in the 3′UTR of the SST gene (4). Taking advantage of the IRES sequence, this strategy allows generating a bicistronic transcript able to code both SST and cre. Unexpectedly, endogenous somatostatin expression is selectively and dose-dependently disrupted in homozygous mutants and the fall in somatostatin levels affects neuroendocrine and physiological responses, mirroring the previously reported dramatic changes observed in SST KO mice (11,13). Using UCSC Genome Browser tools, we did not evidence any conserved motives of transcription factor sites, chip-seq positive signals, or predicted miRNA signals in this part of the SST 3′UTR. The decrease in expression reported here can possibly reflect a structural sensitivity of the mouse SST gene, as already suggested for the transcriptional repressor methyl-CpG binding protein 2 (MeCP2) effect on SST gene expression (19). Thus, cautious examinations of the other SOM-Cre strains available with distinct targeting sites for transgene integration (4,14,20) is needed. While SST expression is selectively impaired in SOM-Cre transgenic mice, no major changes were found concerning SSTR expression and expression levels of the typical peptides or markers assayed in the different brain structures. Except for SST, heterozygous expression profiles were always similar to WT, showing no main significant differences with homozygous mice. Molecular and biochemical approaches quantified the decrease in SOM levels that was also evidenced when comparing in situ hybridization data available in Allen Brain Atlas. This indeed suggests that there is reduced Cre labeling in Sst-IRES-Cre SOM cortex as compared to Sst labeling in C57Bl/6 mice at similar cortical levels [ (14); http://mouse.brain-map.org].
SOM decrease per se correlates well with the neuroendocrine readouts previously shown in SST KO mice, either the dimorphic GH-dependent hepatic genes or the higher CORT response to restraint stress. This strongly supports the hypothesis that SOM is required for masculinization of the GH axis and behavioral emotionality control, as previously demonstrated in recent studies (11,13,21). Conversely, neuroendocrine function did not correlate with behavioral emotionality since no major emotional phenotype was found in the behavioral studies (Figure 3) as previously reported for SST KO males and females (11,13,21). No significant basal plasma CORT difference was found between WT and SOM-Cre or SST KO homozygous animals in the present study, while stress response was strongly enhanced in the SOM-Cre Tg/Tg mice, as previously reported for SST KO (11). Herein, as in Adams' study, mice were housed individually for the behavioral and restraint test, a condition that favors the emergence of stress susceptibility. This may explain the differences observed with Lin and Sibille study (21) where basal levels are different and response to acute stress is similar to WT levels. Nonetheless, increased expression in SOM-Cre Tg/Tg males of the serpina6 gene, coding the corticosterone binding protein, which traps major circulating corticosterone at the periphery, mirrors plasma CORT increase as previously reported in SST KO mice (11,13).
In conclusion, inserting cre transgene in sst 3′UTR alleledependently knocks down endogenous SOM expression in the Sst tm2.1(cre)Zjh /J mice. Therefore, such limitations should be taken into account for conditional KO (cre-lox) studies. On the contrary, these mice may serendipitously constitute an interesting model to study the functional consequences of the gradual changes of somatostatin, which take place (i) transiently during brain development [see Ref. (22) for review] and (ii) in an irreversible manner in major neurological and psychiatric diseases such as Alzheimer's disease, major depression, and schizophrenia (1,21,23,24). aUThOr cOnTriBUTiOns CV and JE designed and supervised the study and they wrote the manuscript, AS performed the immunohistochemical experiments, DG the biochemical assays, VT and AL performed the GH study, GM the Cort experiments, and YL-M and MS bioinformatic survey of the SST promoter. CV performed molecular biology and behavioral experiments, analyzed all data, and prepared the figures.

acKnOWleDgMenTs
We are grateful to Dr. P. Zizzari (U1215 Inserm, Bordeaux) for Cort measurements, P r JL Guillou (UMR5287 CNRS, Bordeaux) for forced-swim test data analysis, Y. Marie and D. Bouteiller for excellent service at PFGS facility (ICM, Paris), D. Geny at CPN imaging facility, and R. A. Piskorowski for text editing. We also thank A. Cougnon, C. Got, and J. Cognet at CPN animal facility for animal care and genotyping and their technical support.