- Research article
- Open Access
Deficiency of 14-3-3ε and 14-3-3ζ by the Wnt1 promoter-driven Cre recombinase results in pigmentation defects
BMC Research Notes volume 9, Article number: 180 (2016)
The seven 14-3-3 protein isoforms bind to numerous proteins and are involved in a wide variety of cellular events, including the cell cycle, cell division, apoptosis and cancer. We previously found the importance of 14-3-3 proteins in neuronal migration of pyramidal neurons in the developing cortex. Here, we test the function of 14-3-3 proteins in the development of neural crest cells in vivo using mouse genetic approaches.
We found that 14-3-3 proteins are important for the development of neural crest cells, in particular for the pigmentation of the fur on the ventral region of mice.
Our data obtained from the 14-3-3ε/14-3-3ζ/Wnt1-Cre mice strongly indicate the importance of 14-3-3 proteins in the development of melanocyte lineages.
The 14-3-3 protein family is composed of seven isoforms, which are encoded by separate genes . By producing and analyzing 14-3-3ε conditional knockout mice and 14-3-3ζ conventional knockout mice, we found that these 14-3-3 proteins are important for neurogenesis of neuronal progenitor cells and neuronal migration of pyramidal neurons in the developing cortex [2, 3]. Also, these knockout mice showed several behavioral defects, such as learning and memory defects and seizures [2, 4, 5]. In addition to the importance of 14-3-3 proteins in neural development and neurological diseases, 14-3-3ε is important for proper heart development . Taken together with the fact that 14-3-3 proteins are important for other cellular events including cancer development and metabolism [7–10], it is evident that 14-3-3 proteins are important for multiple cellular events which are essential for the correct development and function of a variety of tissues.
The repeated-epilation (Er) mutant mouse, as first reported by Hunsicker in 1960, is characterized by a loss of hair induced by radiation exposure . Homozygote Er mice die at birth while heterozygotes develop normally, followed by excessive hair loss resulting in a sparse coat. Li et al.  showed that the repeated epilation is caused by a single nucleotide insertion in the Sfn gene, encoding the 14-3-3σ protein. In addition, they found that the skin defects seen in these mice are the result of abnormal epidermal differentiation. Thus, this indicates that 14-3-3σ proteins are important for the proper development of the epidermis.
Miller-Dieker syndrome is characterized by severe lissencephaly caused by neuronal migration defects as well as craniofacial defects  and is caused by a chromosomal deletion in the 17p13.3 region where the Lis1 (PAFAH1B1) and 14-3-3ε (YWHAE) genes are localized. The 14-3-3ε and Lis1 knockout mice do not show any craniofacial defects, suggesting that the 14-3-3ε protein is not important for craniofacial development. In general, 14-3-3 proteins have to form homodimers or heterodimers to function inside cells, depending on each 14-3-3 isoform. Although 14-3-3ε proteins are able to form functional homodimers, they predominantly form heterodimers with 14-3-3ζ ( and our unpublished observations). Therefore, we tested if 14-3-3ε and 14-3-3ζ double knockouts show any craniofacial defects resulting from defects in neural crest cell development. We achieved this by producing 14-3-3ε/14-3-3ζ double knockout mice using Wnt1-Cre transgenic mice in which Cre recombinase is expressed in neural crest cells [15–17].
To analyze the functions of the 14-3-3ε and 14-3-3ζ proteins in neural crest cells, we utilized mouse genetic approaches using 14-3-3ε conditional (flox) knockout mice, 14-3-3ζ conventional knockout (KO) mice and Wnt1-Cre transgenic mice in which Cre recombinase is expressed in the neural crest cells . Although the complete double knockout (14-3-3ε fl/fl /14-3-3ζ −/− /Wnt1-Cre +) mice were embryonic lethal, the 14-3-3ε +/fl /ζ −/− /Cre + mice are able to survive to adulthood (Table 1). However, the survival rate of the 14-3-3ε +/fl /ζ −/− /Cre + mice was lower than expected (Table 1, observed: n = 5, expected: n = 12), and they show decreased weight compared to the control 14-3-3ε +/+ /ζ +/+ /Cre + mice (Fig. 1, Control: 14.58 g ± 2.58, 14-3-3ε +/fl /ζ −/− /Cre +: 7.98 g ± 2.26).
The 14-3-3ε +/fl /ζ +/− /Cre + mice, 14-3-3ε +/fl /ζ −/− /Cre + mice, 14-3-3ε fl/fl /ζ +/+ /Cre + mice and the 14-3-3ε fl/fl /ζ +/− /Cre + mice had white patches of fur on the ventral region of their torso (Fig. 2 and Table 2, 14-3-3ε +/fl /ζ +/− /Cre + mice: 88.5 %, 14-3-3ε +/fl /ζ −/− /Cre + mice: 80.0 %, 14-3-3ε fl/fl /ζ +/+ /Cre + mice: 80.0 %, and 14-3-3ε fl/fl /ζ +/− /Cre + mice: 100 %). Interestingly, the 14-3-3ε +/fl /ζ +/+ /Cre + and the 14-3-3ε +/+ /ζ −/− /Cre + mice did not show this phenotype. However, 14-3-3ε fl/fl /ζ +/+ /Cre + mice did show white patches on their ventral region. The white patches were observed only on the ventral region of their torso, but not on the tail and paws or any other region. Next, we measured the area of the white patches in each genotype and summarized in Table 3 (14-3-3ε +/fl /ζ +/− /Cre + mice: 0.69 cm2, 14-3-3ε +/fl /ζ −/− /Cre + mice: 1.09 cm2, 14-3-3ε fl/fl /ζ +/+ /Cre + mice: 0.23 cm2, and 14-3-3ε fl/fl /ζ +/− /Cre + mice: 0.97 cm2). We found that the 14-3-3ε +/fl /ζ +/− /Cre + mice, the 14-3-3ε +/fl /ζ −/− /Cre + mice, and the 14-3-3ε fl/fl /ζ +/− /Cre + mice have larger white patches than the 14-3-3ε fl/fl /ζ +/+ /Cre + mice. This indicates that neither14-3-3ε or 14-3-3ζ is dominant in regulating the size of the white patches. Together, these data suggest the importance of the 14-3-3 proteins in melanocyte development.
We also analyzed the craniofacial region for defects since Cre recombinase is also expressed in the craniofacial region (Fig. 3). However, we were not able to find any pronounced defects in the craniofacial region. Further research should be performed to analyze the functions of 14-3-3 proteins in craniofacial development (see the “Discussion” section).
We found that the 14-3-3ε/14-3-3ζ/Wnt1-Cre mice had white patches in their fur on the ventral region of their torso. In the Wnt1-Cre mice, Cre recombinase is expressed in neural crest cells which differentiate into a variety of cells, including melanocytes . A previous study using Wnt1-Cre mice showed that the AP-2α transcription factor knockout mice had white patches similar to those seen in the 14-3-3ε/14-3-3ζ/Wnt1-Cre mice . Neural crest cells are initially generated in the roof plate of the neural tube and migrate and differentiated into specific cells such as melanocytes. Therefore, 14-3-3 proteins could be involved in the migration and differentiation of neural crest cells. Also, it could be possible that 14-3-3 proteins are involved in melanin production in melanocytes. In addition, we cannot exclude the possibility that 14-3-3ζ is important for proper development of neural crest cells because the 14-3-3ε +/fl /ζ +/− /Cre + and 14-3-3ε +/fl /ζ −/− /Cre + mice showed white patches, but not the 14-3-3ε +/fl /ζ +/+ /Cre + (Table 2). To avoid the potential functional compensation by other 14-3-3 isoforms during embryonic development, it may be needed to analyze the functions of the 14-3-3ζ protein in pigmentation by creating and analyzing the 14-3-3ζ conditional knockout mice in conjunction with the Wnt1-Cre transgenic mice.
Although there is no statistical significance in the difference in the weight between the 14-3-3ε +/fl /ζ −/− /Cre − and 14-3-3ε +/fl /ζ −/− /Cre + mice (Fig. 1), the 14-3-3ε +/fl /ζ −/− /Cre + mice tend to be smaller than the 14-3-3ε +/fl /ζ −/− /Cre − mice (Fig. 1). Obviously, the 14-3-3ζ deficiency results in the smaller body size (Fig. 1). Interestingly, the 14-3-3ε gene was removed by Wnt1 promoter-driven Cre recombinase although 14-3-3ζ was deleted in all tissues. Therefore, these data suggest that the deletion of the 14-3-3ε protein by Wnt1 promoter-driven Cre recombinases is responsible for the smaller body size in addition to the 14-3-3ζ deficiency. In addition to neural crest cells, Cre recombinase is expressed in the midbrain/hindbrain junction [16, 20]. Although food consumption was not recorded, it has previously been shown that the hypothalamus is important for controlling feeding behavior . Although the expression of Cre recombinase in the hypothalamus has not been analyzed in Wnt1-Cre transgenic mice, Wnt1 mRNA is expressed in the hypothalamus, suggesting the potential expression of Cre recombinase in the hypothalamus in the Wnt1-Cre mice . Also, a previous study indicated that Cre recombinase is expressed in the pituitary in Wnt1-Cre mice . It is also known that the functional interaction between the hypothalamus and the pituitary is essential for their functions. Therefore, it is possible that the 14-3-3ε protein is important for the proper function of the hypothalamus and the pituitary and may alter feeding behavior and weight maintenance. To test this hypothesis, the specific ablation of 14-3-3ε in these tissues will need to be analyzed in the future.
In addition to pigmentation defects, it is possible that the ablation of 14-3-3ε and 14-3-3ζ in neural crest cells results in severe defects in other organs and tissues, such as the gastrointestinal tract and thyroid, potentially explaining the lower body weight seen in the 14-3-3ε/14-3-3ζ/Wnt1-Cre mice. The enteric nervous system in the gastrointestinal (GI) system is derived from neural crest cells [24, 25]. The enteric nervous system is required for the proper movement of food along the entire GI tract . Disruption of the enteric nervous system therefore could directly impact food uptake and processing and thus interrupt normal growth and weight gain. Therefore, it is possible that the 14-3-3ε/14-3-3ζ/Wnt1-Cre mice have defects in GI peristalsis. Also, parafollicular cells, also called C cells in the thyroid, are derived from neural crest cells and secrete calcitonin involved in the regulation of calcium metabolism . Parafollicular cells also secrete other small peptides such as somatostatin and serotonin, and are involved in thyroid hormone production [28, 29]. Therefore, it is possible that the 14-3-3ε/14-3-3ζ/Wnt1-Cre mice have defects in controlling hormone production in the hypothalamic-pituitary-thyroid axis due to a dysfunction in these cells or in their localization in the thyroid, which is essential for the regulation of metabolism [28, 29]. Thus, further research should be performed to investigate these potential defects by measuring the concentration of the hormones, such as thyroid stimulating hormone (TSH), T3 and T4, in the 14-3-3ε/14-3-3ζ/Wnt1-Cre mice.
Regarding the craniofacial development in the 14-3-3ε/14-3-3ζ/Wnt1-Cre mice, we were not able to find any significant defects in the craniofacial region. However, more research on this topic needs to be undertaken before reaching a conclusion. Further experiments including histology and immunohistochemistry such as bone staining by Alcian Blue/Alizarin Red should be done. Also, it is very helpful for better understanding the mechanisms of craniofacial development to use other Cre transgenic mice, including earlier developmental Cre expression than the Wnt1 promoter can provide, and compare the results obtained from the analyses using these different Cre transgenic mice. The P0 (protein 0)-Cre transgenic mouse is another frequently used mouse line in which Cre recombinase is expressed in epithelial layers of developing tooth germ and taste buds . Also, another Cre transgenic line, tamoxifen-inducible Sox10-Cre transgenic mice in which the expression of Cre recombinases can be regulated by the administration of tamoxifen, will be useful to analyze potential defects in greater detail [31, 32]. Thus, a combinatorial use of a different Cre transgenic mouse lines will provide knowledge for understanding the precise mechanisms of craniofacial development.
Analysis of the functions of 14-3-3ε and 14-3-3ζ proteins indicates their importance in the development of neural crest cells, in particular the development of the melanocyte lineage. Also, our data suggest that the 14-3-3ε proteins are important for weight modulation during development.
The 14-3-3ε conditional (flox) mice and the 14-3-3ζ conventional knockout (KO) mice are described previously [2, 4]. The 14-3-3ε flox mice and the 14-3-3ζ KO mice have been maintained in the 129 genetic background by continuing to backcross them with 129SVE inbred strain (Taconic Biosciences, Inc.) for more than twenty generations. The Wnt1-Cre transgenic mice were obtained from the Jackson Laboratory (STOCK Tg (Wnt1-cre) 11Rth Tg (Wnt1-GAL4)11Rth/MileJ, C57BL/6 genetic background) and have been maintained by crossing with 129SVE. Therefore, all mice used in this study were congenic strain with 129SVE genetic background. Genotyping was performed using tail clippings and PCR with specific primers as previously described [2, 4, 18]. All experiments were performed following protocols approved by the Drexel University Animal Care and Use Committees.
Statistical analysis of mouse weight was performed using Prism (GraphPad Software). The data were analyzed by one-way ANOVA with the Bonferroni post hoc test. Results were deemed statistically significant if the p value was <0.05. *p < 0.05 and **p < 0.01.
analysis of variance
Yaffe MB. How do 14-3-3 proteins work?—Gatekeeper phosphorylation and the molecular anvil hypothesis. FEBS Lett. 2002;513(1):53–7.
Toyo-oka K, Wachi T, Hunt RF, Baraban SC, Taya S, Ramshaw H, et al. 14-3-3ε and ζ regulate neurogenesis and differentiation of neuronal progenitor cells in the developing brain. J Neurosci. 2014;34(36):12168–81.
Toyo-oka K, Shionoya A, Gambello MJ, Cardoso C, Leventer R, Ward HL, et al. 14-3-3epsilon is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller–Dieker syndrome. Nat Genet. 2003;34(3):274–85.
Cheah PS, Ramshaw HS, Thomas PQ, Toyo-Oka K, Xu X, Martin S, et al. Neurodevelopmental and neuropsychiatric behaviour defects arise from 14-3-3ζ deficiency. Mol Psychiatry. 2012;17(4):451–66.
Ikeda M, Hikita T, Taya S, Uraguchi-Asaki J, Toyo-oka K, Wynshaw-Boris A, et al. Identification of YWHAE, a gene encoding 14-3-3epsilon, as a possible susceptibility gene for schizophrenia. Hum Mol Genet. 2008;17(20):3212–22.
Kosaka Y, Cieslik KA, Li L, Lezin G, Maguire CT, Saijoh Y, et al. 14-3-3ε plays a role in cardiac ventricular compaction by regulating the cardiomyocyte cell cycle. Mol Cell Biol. 2012;32(24):5089–102.
Kleppe R, Martinez A, Døskeland SO, Haavik J. The 14-3-3 proteins in regulation of cellular metabolism. Semin Cell Dev Biol. 2011;22(7):713–9.
Hermeking H. The 14-3-3 cancer connection. Nat Rev Cancer. 2003;3(12):931–43.
Wilker E, Yaffe MB. 14-3-3 Proteins—a focus on cancer and human disease. J Mol Cell Cardiol. 2004;37(3):633–42.
Freeman AK, Morrison DK. 14-3-3 Proteins: diverse functions in cell proliferation and cancer progression. Semin Cell Dev Biol. 2011;22(7):681–7.
Hunsicker. Repeated epilation, Er. Mouse News Lett. 1960;23:58–9.
Li Q, Lu Q, Estepa G, Verma IM. Identification of 14-3-3sigma mutation causing cutaneous abnormality in repeated-epilation mutant mouse. Proc Natl Acad Sci USA. 2005;102(44):15977–82.
Dobyns WB, Stratton RF, Parke JT, Greenberg F, Nussbaum RL, Ledbetter DH. Miller-Dieker syndrome: lissencephaly and monosomy 17p. J Pediatr. 1983;102(4):552–8.
Chaudhri M, Scarabel M, Aitken A. Mammalian and yeast 14-3-3 isoforms form distinct patterns of dimers in vivo. Biochem Biophys Res Commun. 2003;300(3):679–85.
Chai Y, Jiang X, Ito Y, Bringas P, Han J, Rowitch DH, et al. Fate of the mammalian cranial neural crest during tooth and mandibular morphogenesis. Development. 2000;127(8):1671–9.
Brault V, Moore R, Kutsch S, Ishibashi M, Rowitch DH, McMahon AP, et al. Inactivation of the beta-catenin gene by Wnt1-Cre-mediated deletion results in dramatic brain malformation and failure of craniofacial development. Development. 2001;128(8):1253–64.
Mao Y, Reiprich S, Wegner M, Fritzsch B. Targeted deletion of Sox10 by Wnt1-cre defects neuronal migration and projection in the mouse inner ear. PLoS ONE. 2014;9(4):e94580.
Danielian PS, Muccino D, Rowitch DH, Michael SK, McMahon AP. Modification of gene activity in mouse embryos in utero by a tamoxifen-inducible form of Cre recombinase. Curr Biol. 1998;8(24):1323–6.
Brewer S, Feng W, Huang J, Sullivan S, Williams T. Wnt1-Cre-mediated deletion of AP-2alpha causes multiple neural crest-related defects. Dev Biol. 2004;267(1):135–52.
Huang T, Liu Y, Huang M, Zhao X, Cheng L. Wnt1-cre-mediated conditional loss of Dicer results in malformation of the midbrain and cerebellum and failure of neural crest and dopaminergic differentiation in mice. J Mol Cell Biol. 2010;2(3):152–63.
Bernardis LL, Bellinger LL. The lateral hypothalamic area revisited: ingestive behavior. Neurosci Biobehav Rev. 1996;20(2):189–287.
Magdaleno S, Jensen P, Brumwell CL, Seal A, Lehman K, Asbury A, et al. BGEM: an in situ hybridization database of gene expression in the embryonic and adult mouse nervous system. PLoS Biol. 2006;4(4):e86.
Nakajima M, Watanabe S, Okuyama S, Shen J, Furukawa Y. Restricted growth and insulin-like growth factor-1 deficiency in mice lacking presenilin-1 in the neural crest cell lineage. Int J Dev Neurosci. 2009;27(8):837–43.
Burns AJ, Thapar N. Advances in ontogeny of the enteric nervous system. Neurogastroenterol Motil. 2006;18(10):876–87.
Burns AJ. Migration of neural crest-derived enteric nervous system precursor cells to and within the gastrointestinal tract. Int J Dev Biol. 2005;49(2–3):143–50.
Robinette ML, Colonna M. GI motility: microbiota and macrophages join forces. Cell. 2014;158(2):239–40.
Adams MS, Bronner-Fraser M. Review: the role of neural crest cells in the endocrine system. Endocr Pathol. 2009;20(2):92–100.
Zabel M. Ultrastructural localization of calcitonin, somatostatin and serotonin in parafollicular cells of rat thyroid. Histochem J. 1984;16(12):1265–72.
Morillo-Bernal J, Fernández-Santos JM, Utrilla JC, de Miguel M, García-Marín R, Martín-Lacave I. Functional expression of the thyrotropin receptor in C cells: new insights into their involvement in the hypothalamic-pituitary-thyroid axis. J Anat. 2009;215(2):150–8.
Yamauchi Y, Abe K, Mantani A, Hitoshi Y, Suzuki M, Osuzu F, et al. A novel transgenic technique that allows specific marking of the neural crest cell lineage in mice. Dev Biol. 1999;212(1):191–203.
Matsuoka T, Ahlberg PE, Kessaris N, Iannarelli P, Dennehy U, Richardson WD, et al. Neural crest origins of the neck and shoulder. Nature. 2005;436(7049):347–55.
He F, Soriano P. Sox10ER(T2) CreER(T2) mice enable tracing of distinct neural crest cell populations. Dev Dyn. 2015;244(11):1394–403.
BC performed all experiments and statistical analysis. BC also maintained mouse colonies and set up all mouse mating needed for completing this work. BC wrote a draft of the manuscript and KT finalized it. KT oversaw this project. Both authors read and approved the final manuscript.
We thank Christina M. Stinger and Dr. Richard B. Huneke for their support of mouse maintenance. This work was supported by startup funds from the Department of Neurobiology and Anatomy at Drexel University College of Medicine to KT.
The authors declare that they have no competing interests.