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1.
Int J Mol Sci ; 17(11)2016 Nov 09.
Artículo en Inglés | MEDLINE | ID: mdl-27834851

RESUMEN

The effects of introns, especially the first intron, on the regulation of gene expression remains unclear. Therefore, the objective of the present study was to investigate the transcriptional regulatory function of intron 1 on the chicken growth hormone (cGH) gene in the rat pituitary tumor cell line (GH4-C1). Transient transfection using first-intron-inserted cGH complete coding sequences (CDSs) and non-intron-inserted cGH CDS plasmids, quantitative RT-PCR (qRT-PCR) and western blot assays were used to detect the expression of cGH. The reporter gene assay was also used to investigate the effect of a series of fragments in the first intron of cGH on gene expression in GH4-C1. All of the results revealed that a 200-bp fragment located in the +485/+684 region of intron 1 was essential for repressing the expression of cGH. Further informatics analysis showed that there was a cluster of 13 transcriptional factor binding sites (TFBSs) in the +485/+684 region of the cGH intron 1. Disruption of a glucocorticoid response-like element (the 19-nucleotide sequence 5'-AGGCTTGACAGTGACCTCC-3') containing a T-box motif (TGACCT) located within this DNA fragment increased the expression of the reporter gene in GH4-C1. In addition, an electrophoretic mobility shift assay (EMSA) revealed a glucocorticoid receptor (GR) protein of rat binding to the glucocorticoid response-like element. Together, these results indicate that there is a negative glucocorticoid response-like element (nGRE) located in the +591/+609 region within the first intron of cGH, which is essential for the down-regulation of cGH expression.


Asunto(s)
Regulación de la Expresión Génica , Hormona del Crecimiento/genética , Intrones , Receptores de Glucocorticoides/genética , Elementos de Respuesta , Somatotrofos/metabolismo , Animales , Secuencia de Bases , Sitios de Unión , Línea Celular Tumoral , Pollos , Exones , Glucocorticoides/farmacología , Hormona del Crecimiento/metabolismo , Humanos , Sistemas de Lectura Abierta , Hipófisis/efectos de los fármacos , Hipófisis/metabolismo , Hipófisis/patología , Plásmidos/química , Plásmidos/metabolismo , Unión Proteica , Ratas , Receptores de Glucocorticoides/metabolismo , Somatotrofos/efectos de los fármacos , Somatotrofos/patología , Factores de Transcripción/genética , Factores de Transcripción/metabolismo , Transcripción Genética , Transfección , Transgenes
2.
Int J Mol Sci ; 17(4): 543, 2016 Apr 12.
Artículo en Inglés | MEDLINE | ID: mdl-27077853

RESUMEN

Turtles grow slowly and have a long lifespan. Ultrastructural studies of the pituitary gland in Reeves' turtle (Chinemys reevesii) have revealed that the species possesses a higher nucleoplasmic ratio and fewer secretory granules in growth hormone (GH) cells than other animal species in summer and winter. C. reevesii GH gene was cloned and species-specific similarities and differences were investigated. The full GH gene sequence in C. reevesii contains 8517 base pairs (bp), comprising five exons and four introns. Intron 1 was found to be much longer in C. reevesii than in other species. The coding sequence (CDS) of the turtle's GH gene, with and without the inclusion of intron 1, was transfected into four cell lines, including DF-1 chicken embryo fibroblasts, Chinese hamster ovary (CHO) cells, human embryonic kidney 293FT cells, and GH4C1 rat pituitary cells; the turtle growth hormone (tGH) gene mRNA and protein expression levels decreased significantly in the intron-containing CDS in these cell lines, compared with that of the corresponding intronless CDS. Thus, the long intron 1 of GH gene in Reeves' turtle might correlate with downregulated gene expression.


Asunto(s)
Clonación Molecular/métodos , Hormona del Crecimiento/genética , Intrones , Proteínas de Reptiles/genética , Tortugas/metabolismo , Animales , Células CHO , Línea Celular , Embrión de Pollo , Cricetinae , Cricetulus , Regulación de la Expresión Génica , Células HEK293 , Humanos , Filogenia , Ratas , Especificidad de la Especie , Tortugas/genética
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