The Villin1 Gene Promoter Drives Cre Recombinase Expression in Extraintestinal Tissues.

Villin, encoded by Vil1, is an actin-binding protein expressed by intestinal, hepatobiliary, and renal tubular epithelial cells. Transgenic mice in which the Vil1 promoter drives Cre recombinase expression are widely used to inactivate genes in the intestinal epithelium. The 4 most commonly used Vil1Cre lines were generated by independent groups using distinct promoter constructs., Although these lines have been well-characterized in the intestine, their extraintestinal Cre activity has not been fully defined or compared.

We first studied the Tg(Vil1-cre)997Gum and Tg(Vil1-cre)1000Gum transgenic lines in which a 12.4-kilobase region of the Vil1 promoter drives Cre expression. We crossed them with Rosa26-Ai9 reporter mice, in which Cre-mediated excision of a stop cassette leads to expression of fluorescent TdTomato (Supplementary Methods). Both the Vil1Cre/997 and Vil1Cre/1000 lines exhibited Cre activity in epithelial cells throughout the small intestine and colon, as previously described. Unexpectedly, Cre activity was also evident in specific central nervous system (CNS) nuclei: the anterodorsal thalamic nucleus (important for spatial navigation) and 2 small groups of cholinergic neurons in the medulla (Figure 1). All TdTomato+ cells in these nuclei co-localized with the neuronal marker NeuN, and none expressed the oligodendrocyte marker PLP1 (Figure 1). Consistent with these observations, Vil1 transcripts were reported in a subset of thalamic excitatory neurons at postnatal day 21 but not in the adult mouse CNS (Allen Mouse Brain Atlas), suggesting at least transient expression in these neurons.

Figure 1

The Vil1 promoter drives Cre recombinase expression in the CNS. (A–C) Coronal section from a Vil1Cre/1000 Rosa26Ai9/+ mouse brain shows TdTomato expression in cells within a periventricular region of the forebrain consistent with the anterodorsal thalamic nucleus (A and B) but not in the cerebral cortex (A and C). (D–F) Immunohistochemical staining of a Vil1Cre/1000 Rosa26Ai9/+ mouse brain shows that all TdTomato+ neurons within the anterodorsal thalamus (AD) co-localize with the pan-neuronal marker NeuN (D) but not the glial marker PLP1 (E). Thirty-eight percent ± 15% of NeuN+ neurons in the AD thalamus expressed TdTomato (mean ± standard deviation, n = 3 animals). TdTomato+ neurons are not immunoreactive for GAD67 but are contacted by many GAD67+ puncta, likely the terminals of GABAergic inhibitory neurons (F). (E) is from a mouse that was also hemizygous for the PLP1eGFP transgene. (G–I) Cross sections of brainstem from Vil1Cre/1000 Rosa26Ai9/+ mice show TdTomato expression in the dorsal and ventral medulla. All TdTomato+ cells co-localized with NeuN and ChAT, the biosynthetic enzyme for acetylcholine (shown in H and I for dorsal medulla and boxed region in G). TdTomato+ neurons in the dorsal medulla localized to the nucleus of the solitary tract (boxed region in G) and those in the ventral medulla to the nucleus ambiguus (asterisk in G). Scale bars for A and G = 400 μm; B and C = 75 μmol/L; D–F, H, and I = 25 μm.

The Vil1Cre/997 line also drove patchy Cre-mediated recombination throughout the cerebral cortex (Supplementary Figure 1). In contrast, Vil1Cre/1000 mice had no detectable TdTomato in cells in the cerebral cortex (Figure 1) or spinal cord (Supplementary Figure 1) or within intrinsic and extrinsic nerve fibers innervating the gut (Supplementary Figure 2). Therefore, we focused further characterization on these mice. Vil1Cre/1000 mice exhibited Cre-dependent reporter expression in small areas of the exocrine pancreas, rare epithelial cells within the glandular stomach (consistent with prior studies), and some proximal tubules in the kidney (Supplementary Figures 2 and 3, Table 1). Patchy reporter expression was also detected in oviduct epithelium, but not the uterus, ovary, or testis (Supplementary Figures 3 and 4).

Supplementary Figure 1

Vil1 promoter-driven Cre recombinase expression is present in the brain but undetectable in the spinal cord. (A–C) Coronal sections of brain tissue from an adult Vil1Cre/997 R26Ai9/+ mouse show Cre-dependent TdTomato reporter expression in the anterodorsal thalamic nucleus (A and B) and patchy recombination throughout the cerebral cortex (A and C). Scale bars for A = 400 μm; B and C = 100 μm. (D–I) No Cre-dependent reporter expression was observed in cross sections of dorsal or ventral horn spinal cord (SC) tissue from adult Vil1Cre/1000 R26Ai9/+, Vil1Cre/20 R26mTmG/+, or Vil1CreERT2/23 R26mTmG/+ mice. Scale bars = 50 μm.

Supplementary Figure 2

(A, D, G, J, M) Cross sections of tissue from an adult Vil1Cre/1000 R26Ai9/+ mouse show Cre-dependent TdTomato reporter expression (pseudo-colored green) in rare epithelial cells of the glandular stomach, throughout the epithelia of the small and large intestines, and in isolated exocrine cells of the pancreas. No reporter expression was detected in the esophagus. (B, E, H, K, N) Cross sections of tissue from an adult Vil1Cre/20 R26mTmG/+ mouse show Cre-dependent GFP reporter expression (green) throughout the epithelia of the glandular stomach, small intestine, and colon. Extensive GFP expression was also evident throughout the pancreatic parenchyma, except in blood vessels and islets (which retain TdTomato fluorescence [red] and are morphologically distinct). No GFP was detected in the esophagus. (C, F, I, L, O) Cross sections of tissue from an adult Vil1CreERT2/23 R26mTmG/+ mouse 7 days status post a 5-day course of tamoxifen show Cre-dependent GFP reporter expression (green) in subsets of epithelial cells in the small and large intestines. No GFP was detected in the esophagus, stomach, or pancreas. Scale bars = 25 μm.

Supplementary Figure 3

(A–C) Cre-dependent GFP reporter expression was detected throughout the uterine epithelium in some Vil1Cre/20 R26mTmG/+ mice (such as example shown here), but not the other 2 lines examined. (D–F) Cre-dependent TdTomato reporter expression (pseudo-colored green) is seen in patchy areas of the oviduct epithelium in Vil1Cre/1000 R26Ai9 mice, but not the other 2 lines. (G–I) Cre-dependent GFP reporter expression was detected throughout the bladder epithelium in Vil1Cre/20 R26mTmG/+ mice, but not the other 2 lines. (J–L) Cre-dependent reporter expression was seen in scattered cells in the kidneys of Vil1Cre/1000 R26Ai9 mice and was extensive throughout the renal proximal tubular epithelium in Vil1Cre/20 R26mTmG/+ mice. No reporter expression was detected in Vil1CreERT2/23 R26mTmG/+ mouse kidney. Scale bars = 25 μm.

Table 1

Cre-Dependent Reporter Expression in Tissues From Vil1 Promoter-Driven Transgenic Mouse Lines

	Vil1Cre/1000	Vil1Cre/20	Vil1CreERT2/23
Central nervous system
Brain	Rare neurons	–	–
Spinal cord	–	–	–
Alimentary tract
Tongue	–	–	–
Esophagus	–	–	–
Stomach (nonglandular)	–	–	–
Stomach (glandular)	Rare	Extensive	–
Small intestine	Extensive	Extensive	Patchy
Large intestine	Extensive	Extensive	Patchy
Pancreas	Scattered	Extensive	–
Liver	–	Scattered	–
Urogenital
Kidney	Scattered	Extensive	–
Bladder	–	Extensive	–
Testis	–	Scattered	Scattered
Ovary	–	–	–
Oviduct	Scattered	–	–
Uterus	–	+/–	–
Other
Heart	–	–	–
Lung	–	–	–
Spleen	–	Scattered	–
Adrenal	–	–	–

NOTE. – indicates reporter expression was not detected. +/– indicates patchy reporter expression was detected in some, but not all, animals.

Supplementary Figure 4

The Vil1 promoter drives Cre recombinase expression in the male, but not female, gonads in some transgenic lines. (A, D, G) Cross sections of tissue from adult Vil1Cre/1000 R26Ai9/+ mice show no evident Cre-dependent TdTomato reporter expression (pseudo-colored green) in the testis or the ovary. (B, E, H) Cross sections of tissue from adult Vil1Cre/20 R26mTmG/+ mice show Cre-dependent GFP reporter expression (green) in subset of seminiferous tubules of the testis but no expression in the ovary. (C, F, I) Cross sections of tissue from adult Vil1CreERT2/23 R26mTmG/+ mice 7 days after tamoxifen show Cre-dependent GFP reporter expression (green) in subset of seminiferous tubules of the testis but none in the ovary. Boxed regions in A–C are shown at higher magnification in D–F. Scale bars = 25 μm.

We next examined Tg(Vil1-cre)20Syr and Tg(Vil1-cre/ERT2)23Syr, transgenic lines in which a 9-kilobase region of the Vil1 promoter drives Cre expression. These lines were crossed with Rosa26-mTmG reporter mice in which Cre activity terminates TdTomato expression and activates green fluorescent protein (GFP) expression. Vil1Cre/20 mice exhibited Cre activity in epithelia throughout the small and large intestines (Supplementary Figure 2), as previously described. Cre activity was also detected in the exocrine pancreas and renal proximal tubules to a much greater extent than in Vil1Cre/1000 mice (Supplementary Figures 2 and 3). Unlike Vil1Cre/1000 mice, Vil1Cre/20 mice exhibited diffuse Cre activity in epithelia of the glandular stomach and bladder and patchy activity in liver and spleen (Supplementary Figures 2 and 3, Table 1). Cre activity was also evident in the uterine epithelium of some females (Supplementary Figure 3). There was no GFP expression in oviduct or ovary, but germ cell expression was observed within a subset of seminiferous tubules in the testis in all males, raising the possibility of germline recombination (Supplementary Figure 4).

The Vil1CreERT2/23 line is unique among the 4 lines studied because it expresses a Cre recombinase–estrogen receptor fusion protein that requires tamoxifen to trigger nuclear translocation and recombination. Vil1CreERT2/23 Rosa26mTmG/+ mice were administered tamoxifen daily for 5 doses and then analyzed 7 days after the last dose. Reporter expression was diffuse in the small intestinal epithelium and patchy in the colon (Supplementary Figure 2), as previously described. In contrast to other lines, Cre activity was not detected in the stomach, pancreas, kidney, or female reproductive tract (Supplementary Figure 2, Supplementary Figure 3, Supplementary Figure 4). However, there was reporter expression in germ cells within some seminiferous tubules (Supplementary Figure 4). Neither this line nor the Vil1Cre/20 line exhibited any Cre activity in the nervous system.

These data show that the 4 most commonly used Vil1Cre mouse lines are nonequivalent and have distinct and unexpected sites of extraintestinal Cre expression. Therefore, the Vil1Cre line to be used for any given experiment should be chosen carefully on the basis of the gene of interest and the potential for “off-target” effects outside the gut. The extensive Cre activity in Vil1Cre/997 mouse brains provides particularly strong rationale for selecting Vil1Cre/1000 or Vil1Cre/20 lines as alternatives for most studies. Conversely, although Cre activity within the exocrine pancreas, glandular stomach, and bladder of Vil1Cre/20 mice might be useful for some experiments, it is an important confounding variable in studies where gene deletion in these organs could impact the interpretation of observations attributed to gene functions in the intestinal epithelium. The Vil1CreERT2/23 line was the most selective for the intestinal epithelium, but like any inducible Cre system, it exhibited relatively less recombination than the constitutively active Cre lines. Importantly, both Vil1CreERT2/23 and Vil1Cre/20 lines exhibited Cre activity in a subset of male germ cells, raising concern that when these lines are used to delete genes, some progeny could have globally null alleles. One limitation of our study is that 2 different Cre-reporter lines were used, although both targeted the Rosa26 locus. Recombination efficiency at different loxP sites and genomic loci can vary. Thus, although our findings provide guidance on Cre activity in these 4 Vil1 transgenic lines, it is possible that this activity may manifest differently in the context of other floxed alleles.

Our findings highlight the necessity of rigorously characterizing transgenic lines in all studies to ensure accurate data interpretation and reproducibility. Just as some Cre lines presumed to be selective for the nervous system were later found to be expressed in the germline or gut epithelium,, our data show that Cre lines commonly used to study intestinal epithelial biology can be active in the nervous system and other tissues that might affect gut functions. These observations do not detract from the value of these genetic tools, but they do emphasize the need for careful reagent choice, data interpretation, and methods reporting in all studies using these mice.