Wen L et al. (2019), Thyroid Hormone Receptor Alpha Is Required for ...

XB-ART-56139

Front Endocrinol (Lausanne) 2019 Jan 01;10:396. doi: 10.3389/fendo.2019.00396.

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Thyroid Hormone Receptor Alpha Is Required for Thyroid Hormone-Dependent Neural Cell Proliferation During Tadpole Metamorphosis.

Wen L , He C , Sifuentes CJ , Denver RJ .

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Thyroid hormone (T3) plays several key roles in development of the nervous system in vertebrates, controlling diverse processes such as neurogenesis, cell migration, apoptosis, differentiation, and maturation. In anuran amphibians, the hormone exerts its actions on the tadpole brain during metamorphosis, a developmental period dependent on T3. Thyroid hormone regulates gene transcription by binding to two nuclear receptors, TRα and TRβ. Our previous findings using pharmacological and other approaches supported that TRα plays a pivotal role in mediating T3 actions on neural cell proliferation in Xenopus tadpole brain. Here we used Xenopus tropicalis (X. tropicalis) tadpoles with an inactivating mutation in the gene that encodes TRα to investigate roles for TRα in mitosis and gene regulation in tadpole brain. Gross morphological analysis showed that mutant tadpoles had proportionally smaller brains, corrected for body size, compared with wildtype, both during prometamorphosis and at the completion of metamorphosis. This was reflected in a large reduction in phosphorylated histone 3 (pH3; a mitosis marker) immunoreactive (ir) nuclei in prometamorphic tadpole brain, when T3-dependent cell proliferation is maximal. Treatment of wild type premetamorphic tadpoles with T3 for 48 h induced gross morphological changes in the brain, and strongly increased pH3-ir, but had no effect in mutant tadpoles. Thyroid hormone induction of the direct TR target genes thrb, klf9, and thibz was dysregulated in mutant tadpoles. Analysis of gene expression by RNA sequencing in the brain of premetamorphic tadpoles treated with or without T3 for 16 h showed that the TRα accounts for 95% of the gene regulation responses to T3.

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???displayArticle.link??? Front Endocrinol (Lausanne)

Species referenced: Xenopus tropicalis
Genes referenced: klf9 thibz thra thrb

???displayArticle.gses??? GSE130816: NCBI

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	Figure 1. Brain size and cell proliferation is reduced in thramtâˆ’exon4 animals. We measured body length and brain volume in wild type (WT) and thramtâˆ’exon4 animals at two stages of development. Brain volume was measured on fixed brains as described in the Materials and Methods. Bars are the mean Â± SEM. (A) Comparison of body length and brain volume of WT and thramtâˆ’exon4 prometamorphic tadpoles (NF stage 56; n = 6/genotype). (B) Comparison of body length and brain volume of WT and thramtâˆ’exon4 newly metamorphosed frogs (NF stage 66; n = 8/genotype). (C) Comparison of phosphorylated histone 3 (pH3) immunoreactive nuclei in the brain of WT and thramtâˆ’exon4 NF stage 56 tadpoles (n = 4â€“6/genotype). p < 0.01, p < 0.001, **p < 0.0001, unpaired Student's t-test.
	Figure 2. Thyroid hormone receptor Î± is required for T3-dependent morphological changes, and induction of cell proliferation in tadpole brain. We treated wild type (WT) and thramtâˆ’exon4 premetamorphic (NF stage 54) tadpoles with T3 (5 nM) or vehicle added to the aquarium water for 42 h, then measured brain size and phosphorylated histone 3 immunoreactivity (pH3-ir) in the brain as described in the Materials and Methods. Bars are the mean Â± SEM. (A) Exogenous T3 caused dramatic morphological changes in the brains of WT, but not thramtâˆ’exon4 tadpoles. Shown are dorsal images of fixed tadpole brains. (B) Exogenous T3 decreased length, and increased width of WT tadpole brain, but had no effect in thramtâˆ’exon4 animals (***p < 0.0001, unpaired Student's t-test). In vehicle-treated tadpoles, the baseline brain length and width were both smaller in thramtâˆ’exon4 compared with WT (###p < 0.0001, unpaired Student's t-test). (C) Treatment with T3 strongly increased pH3-ir in WT (p < 0.0001, unpaired Student's t-test), but decreased it in thramtâˆ’exon4 tadpole brain (p < 0.0001). Shown is the fold change in total brain pH3-ir nuclei in each genotype. The dashed line indicates fold change of 1.0 = no change.
	Figure 3. Gene transcription responses to exogenous T3 are impaired in thramtâˆ’exon4 tadpole brain. We treated wild type (WT) and thramtâˆ’exon4 premetamorphic (NF stage 54) tadpoles with T3 (5 nM) or vehicle added to the aquarium water for different times, then measured target gene mRNA levels in brain (region of the preoptic area/thalamus/hypothalamus) by RTqPCR using absolute quantification (for thra and thrb, panel A) or relative quantification (genes in panel B). (A) Thyroid hormone receptor Î± is the major TR subtype expressed in tadpole brain. Comparison of baseline mRNA levels, and effects of T3 treatment for 42 h on thra and thrb mRNA levels in WT and thramtâˆ’exon4 tadpole brain. Bars represent the mean Â± SEM (n = 4/genotype/treatment). Note that the baseline (vehicle-treated) thra mRNA level is 14 times greater than thrb mRNA in WT tadpole brain. The baseline thra mRNA was significantly lower, while the thrb mRNA was significantly higher in thramtâˆ’exon4 compared with WT tadpole brain (##p < 0.001, Student's unpaired t-test). Treatment with T3 had no effect on thra mRNA, but strongly induced thrb mRNA in both genotypes (p < 0.001, *p < 0.0001, Student's unpaired t-test). (B) Venn diagram representing the numbers of T3-regulated genes determined by RNA-seq conducted on RNA isolated from brains of wild type and thramtâˆ’exon4 NF stage 54 tadpoles treated with or without T3 for 16 h. (C) Time course of induction by T3 in tadpole brain of mRNAs for three direct T3 response genes, thrb, klf9, and thibz (note that these three genes are included in the 178 genes that overlap between WT and thramtâˆ’exon4). Points represent the mean Â± SEM (n = 4/genotype/time point). The mRNA level for each of the genes was elevated at 8 h in both genotypes (p < 0.001, ANOVA), and the slope of each curve was significantly different between WT and thramtâˆ’exon4 (p < 0.0001, linear regression analysis).
	Figure 4. RNA sequencing shows that the majority of gene regulation responses to exogenous T3 are lost in thramtâˆ’exon4 tadpole brain. We treated wild type (WT) and thramtâˆ’exon4 premetamorphic (NF stage 54) tadpoles with T3 (5 nM) added to the aquarium water for 16 h, then analyzed mRNA levels in brain (region of the preoptic area/thalamus/hypothalamus) by RNA-sequencing or RTqPCR using relative quantification. (A) Venn diagram representing the numbers of T3-induced genes determined by RNA-sequencing conducted on RNA isolated from tadpole brains treated with or without T3. (B) Validation of gene regulation for four T3-induced genes found within the overlap between the WT and thramtâˆ’exon4 gene sets (109 genes). (C) Venn diagram representing the numbers of T3-repressed genes determined by RNA-sequencing conducted on RNA isolated from tadpole brains treated with or without T3. (D) Validation of gene regulation for four T3-repressed genes found within the overlap between the WT and thramtâˆ’exon4 gene sets (69 genes). Bars represent the mean Â± SEM (n = 4/genotype/treatment). For comparisons of vehicle with T3 treated: p < 0.01, p < 0.001, **p < 0.0001, Student's unpaired t-test. For comparisons of baseline mRNA levels (vehicle treated) among the two genotypes: #p < 0.01, Student's unpaired t-test.
	Figure 5. Effects of loss of TRÎ± on baseline gene transcription in premetamorphic tadpole brain. We treated wild type (WT) and thramtâˆ’exon4 premetamorphic (NF stage 54) tadpoles with T3 (5 nM) added to the aquarium water for 16 h, then analyzed mRNA levels in brain (region of the preoptic area/thalamus/hypothalamus; including the pituitary) by RNA-sequencing or RTqPCR using relative quantification. (A) Venn diagram representing the number of T3-induced genes in WT and the number of genes whose baseline mRNA level was elevated in thramtâˆ’exon4 tadpoles, determined by RNA-sequencing conducted on RNA isolated from tadpole brains treated with or without T3. (B) Validation of gene regulation for two T3-induced genes found within the overlap between the T3 induced WT and elevated baseline in thramtâˆ’exon4 gene sets (74 genes). (C) Venn diagram representing the number of T3-repressed genes in WT and the number of genes whose baseline mRNA level was reduced in thramtâˆ’exon4 tadpoles, determined by RNA-sequencing conducted on RNA isolated from tadpole brains treated with or without T3. (D) Validation of gene regulation for two T3-repressed genes found within the overlap between the T3 repressed WT and reduced baseline in thramtâˆ’exon4 gene sets (78 genes). Bars represent the mean Â± SEM (n = 4/genotype/treatment). For comparisons of vehicle with T3 treated: p < 0.01, p < 0.001, **p < 0.0001, Student's unpaired t-test. For comparisons of baseline mRNA levels (vehicle treated) among the two genotypes: #p < 0.01, Student's unpaired t-test.

References [+] :

Bagamasbad, A role for basic transcription element-binding protein 1 (BTEB1) in the autoinduction of thyroid hormone receptor beta. 2008, Pubmed, Xenbase

	Figure 1. Brain size and cell proliferation is reduced in thramtâˆ’exon4 animals. We measured body length and brain volume in wild type (WT) and thramtâˆ’exon4 animals at two stages of development. Brain volume was measured on fixed brains as described in the Materials and Methods. Bars are the mean Â± SEM. (A) Comparison of body length and brain volume of WT and thramtâˆ’exon4 prometamorphic tadpoles (NF stage 56; n = 6/genotype). (B) Comparison of body length and brain volume of WT and thramtâˆ’exon4 newly metamorphosed frogs (NF stage 66; n = 8/genotype). (C) Comparison of phosphorylated histone 3 (pH3) immunoreactive nuclei in the brain of WT and thramtâˆ’exon4 NF stage 56 tadpoles (n = 4â€“6/genotype). p < 0.01, p < 0.001, **p < 0.0001, unpaired Student's t-test.
	Figure 2. Thyroid hormone receptor Î± is required for T3-dependent morphological changes, and induction of cell proliferation in tadpole brain. We treated wild type (WT) and thramtâˆ’exon4 premetamorphic (NF stage 54) tadpoles with T3 (5 nM) or vehicle added to the aquarium water for 42 h, then measured brain size and phosphorylated histone 3 immunoreactivity (pH3-ir) in the brain as described in the Materials and Methods. Bars are the mean Â± SEM. (A) Exogenous T3 caused dramatic morphological changes in the brains of WT, but not thramtâˆ’exon4 tadpoles. Shown are dorsal images of fixed tadpole brains. (B) Exogenous T3 decreased length, and increased width of WT tadpole brain, but had no effect in thramtâˆ’exon4 animals (***p < 0.0001, unpaired Student's t-test). In vehicle-treated tadpoles, the baseline brain length and width were both smaller in thramtâˆ’exon4 compared with WT (###p < 0.0001, unpaired Student's t-test). (C) Treatment with T3 strongly increased pH3-ir in WT (p < 0.0001, unpaired Student's t-test), but decreased it in thramtâˆ’exon4 tadpole brain (p < 0.0001). Shown is the fold change in total brain pH3-ir nuclei in each genotype. The dashed line indicates fold change of 1.0 = no change.
	Figure 3. Gene transcription responses to exogenous T3 are impaired in thramtâˆ’exon4 tadpole brain. We treated wild type (WT) and thramtâˆ’exon4 premetamorphic (NF stage 54) tadpoles with T3 (5 nM) or vehicle added to the aquarium water for different times, then measured target gene mRNA levels in brain (region of the preoptic area/thalamus/hypothalamus) by RTqPCR using absolute quantification (for thra and thrb, panel A) or relative quantification (genes in panel B). (A) Thyroid hormone receptor Î± is the major TR subtype expressed in tadpole brain. Comparison of baseline mRNA levels, and effects of T3 treatment for 42 h on thra and thrb mRNA levels in WT and thramtâˆ’exon4 tadpole brain. Bars represent the mean Â± SEM (n = 4/genotype/treatment). Note that the baseline (vehicle-treated) thra mRNA level is 14 times greater than thrb mRNA in WT tadpole brain. The baseline thra mRNA was significantly lower, while the thrb mRNA was significantly higher in thramtâˆ’exon4 compared with WT tadpole brain (##p < 0.001, Student's unpaired t-test). Treatment with T3 had no effect on thra mRNA, but strongly induced thrb mRNA in both genotypes (p < 0.001, *p < 0.0001, Student's unpaired t-test). (B) Venn diagram representing the numbers of T3-regulated genes determined by RNA-seq conducted on RNA isolated from brains of wild type and thramtâˆ’exon4 NF stage 54 tadpoles treated with or without T3 for 16 h. (C) Time course of induction by T3 in tadpole brain of mRNAs for three direct T3 response genes, thrb, klf9, and thibz (note that these three genes are included in the 178 genes that overlap between WT and thramtâˆ’exon4). Points represent the mean Â± SEM (n = 4/genotype/time point). The mRNA level for each of the genes was elevated at 8 h in both genotypes (p < 0.001, ANOVA), and the slope of each curve was significantly different between WT and thramtâˆ’exon4 (p < 0.0001, linear regression analysis).
	Figure 4. RNA sequencing shows that the majority of gene regulation responses to exogenous T3 are lost in thramtâˆ’exon4 tadpole brain. We treated wild type (WT) and thramtâˆ’exon4 premetamorphic (NF stage 54) tadpoles with T3 (5 nM) added to the aquarium water for 16 h, then analyzed mRNA levels in brain (region of the preoptic area/thalamus/hypothalamus) by RNA-sequencing or RTqPCR using relative quantification. (A) Venn diagram representing the numbers of T3-induced genes determined by RNA-sequencing conducted on RNA isolated from tadpole brains treated with or without T3. (B) Validation of gene regulation for four T3-induced genes found within the overlap between the WT and thramtâˆ’exon4 gene sets (109 genes). (C) Venn diagram representing the numbers of T3-repressed genes determined by RNA-sequencing conducted on RNA isolated from tadpole brains treated with or without T3. (D) Validation of gene regulation for four T3-repressed genes found within the overlap between the WT and thramtâˆ’exon4 gene sets (69 genes). Bars represent the mean Â± SEM (n = 4/genotype/treatment). For comparisons of vehicle with T3 treated: p < 0.01, p < 0.001, **p < 0.0001, Student's unpaired t-test. For comparisons of baseline mRNA levels (vehicle treated) among the two genotypes: #p < 0.01, Student's unpaired t-test.
	Figure 5. Effects of loss of TRÎ± on baseline gene transcription in premetamorphic tadpole brain. We treated wild type (WT) and thramtâˆ’exon4 premetamorphic (NF stage 54) tadpoles with T3 (5 nM) added to the aquarium water for 16 h, then analyzed mRNA levels in brain (region of the preoptic area/thalamus/hypothalamus; including the pituitary) by RNA-sequencing or RTqPCR using relative quantification. (A) Venn diagram representing the number of T3-induced genes in WT and the number of genes whose baseline mRNA level was elevated in thramtâˆ’exon4 tadpoles, determined by RNA-sequencing conducted on RNA isolated from tadpole brains treated with or without T3. (B) Validation of gene regulation for two T3-induced genes found within the overlap between the T3 induced WT and elevated baseline in thramtâˆ’exon4 gene sets (74 genes). (C) Venn diagram representing the number of T3-repressed genes in WT and the number of genes whose baseline mRNA level was reduced in thramtâˆ’exon4 tadpoles, determined by RNA-sequencing conducted on RNA isolated from tadpole brains treated with or without T3. (D) Validation of gene regulation for two T3-repressed genes found within the overlap between the T3 repressed WT and reduced baseline in thramtâˆ’exon4 gene sets (78 genes). Bars represent the mean Â± SEM (n = 4/genotype/treatment). For comparisons of vehicle with T3 treated: p < 0.01, p < 0.001, **p < 0.0001, Student's unpaired t-test. For comparisons of baseline mRNA levels (vehicle treated) among the two genotypes: #p < 0.01, Student's unpaired t-test.