The emergence of the vasopressin and oxytocin hormone receptor gene family lineage: Clues from the characterization of vasotocin receptors in the sea lamprey (Petromyzon marinus)

2016 ◽  
Vol 226 ◽  
pp. 88-101 ◽  
Author(s):  
Sally A. Mayasich ◽  
Benjamin L. Clarke
1989 ◽  
Vol 9 (10) ◽  
pp. 4213-4219
Author(s):  
M A Watson ◽  
J Milbrandt

The NGFI-B cDNA was previously isolated by virtue of its induction by nerve growth factor (NGF) in PC12 cells. It encodes a 61-kilodalton protein that has two regions of extensive homology with members of the steroid/thyroid hormone receptor gene family. The rat NGFI-B gene is approximately 7.6 kilobases long and is interrupted by six introns. Although the exon-intron structure of the gene is similar to those of several other members of the steroid/thyroid hormone receptor gene family, there is a novel splice site within the DNA-binding domain which suggests that NGFI-B constitutes yet another evolutionary digression from a postulated common ancestral receptor gene. Primer extension and S1 nuclease protection assays were used to determine the transcription initiation site, which displayed the heterogeneity typical of genes that lack a TATA box. Sequence analysis of the 5' flanking region revealed several GC boxes but no identifiable TATA box. Four potential AP1 binding sites were identified at nucleotides -49, -78, -222, and -242. Neither the serum response element nor the CArG box element, two sequences found in other growth factor-inducible genes, was detected in this region of the growth factor-inducible NGFI-B gene. Nevertheless, results of nuclear runoff experiments demonstrated that the NGFI-B gene was transcriptionally activated by nerve growth factor in PC12 cells. In vivo, a rapid, dramatic increase in NGFI-B mRNA was observed in the cerebral cortex, midbrain, and cerebellum of animals that experienced a convulsant-induced seizure.


1989 ◽  
Vol 9 (10) ◽  
pp. 4213-4219 ◽  
Author(s):  
M A Watson ◽  
J Milbrandt

The NGFI-B cDNA was previously isolated by virtue of its induction by nerve growth factor (NGF) in PC12 cells. It encodes a 61-kilodalton protein that has two regions of extensive homology with members of the steroid/thyroid hormone receptor gene family. The rat NGFI-B gene is approximately 7.6 kilobases long and is interrupted by six introns. Although the exon-intron structure of the gene is similar to those of several other members of the steroid/thyroid hormone receptor gene family, there is a novel splice site within the DNA-binding domain which suggests that NGFI-B constitutes yet another evolutionary digression from a postulated common ancestral receptor gene. Primer extension and S1 nuclease protection assays were used to determine the transcription initiation site, which displayed the heterogeneity typical of genes that lack a TATA box. Sequence analysis of the 5' flanking region revealed several GC boxes but no identifiable TATA box. Four potential AP1 binding sites were identified at nucleotides -49, -78, -222, and -242. Neither the serum response element nor the CArG box element, two sequences found in other growth factor-inducible genes, was detected in this region of the growth factor-inducible NGFI-B gene. Nevertheless, results of nuclear runoff experiments demonstrated that the NGFI-B gene was transcriptionally activated by nerve growth factor in PC12 cells. In vivo, a rapid, dramatic increase in NGFI-B mRNA was observed in the cerebral cortex, midbrain, and cerebellum of animals that experienced a convulsant-induced seizure.


Nature ◽  
1984 ◽  
Vol 312 (5996) ◽  
pp. 779-781 ◽  
Author(s):  
Roger Miesfeld ◽  
Sam Okret ◽  
Ann-Charlotte Wikström ◽  
Örjan Wrange ◽  
Jan-Åke Gustafsson ◽  
...  

2019 ◽  
Vol 208 ◽  
pp. 106109
Author(s):  
Adamu Mani Isa ◽  
Martha N. Bemji ◽  
Mathew Wheto ◽  
Tolulope J. Williams ◽  
Eveline M. Ibeagha-Awemu

Gene ◽  
2007 ◽  
Vol 395 (1-2) ◽  
pp. 135-143 ◽  
Author(s):  
Christoph Knorr ◽  
Christian Beuermann ◽  
Julia Beck ◽  
Bertram Brenig

2007 ◽  
Vol 0 (0) ◽  
pp. 070717083332002-??? ◽  
Author(s):  
J. Bohbot ◽  
R. J. Pitts ◽  
H.-W. Kwon ◽  
M. Rützler ◽  
H. M. Robertson ◽  
...  

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