CRISPR/Cas9-Based Genome Editing of Transcription Factor Genes in Marchantia polymorpha

Author(s):  
Shigeo S. Sugano ◽  
Ryuichi Nishihama
PLoS ONE ◽  
2014 ◽  
Vol 9 (11) ◽  
pp. e111841 ◽  
Author(s):  
Francisco Javier Buitrago-Flórez ◽  
Silvia Restrepo ◽  
Diego Mauricio Riaño-Pachón

2018 ◽  
Vol 61 (2) ◽  
pp. 85-96 ◽  
Author(s):  
Hongwei Xun ◽  
Zhibing Zhang ◽  
Yunxiao Zhou ◽  
Xueyan Qian ◽  
Yingshan Dong ◽  
...  

2021 ◽  
Author(s):  
Martin A. Mecchia ◽  
Mariano García-Hourquet ◽  
Fidel Lozano-Elena ◽  
Ainoa Planas-Riverola ◽  
David Blasco-Escamez ◽  
...  

2006 ◽  
Vol 154 (1) ◽  
pp. 159-166 ◽  
Author(s):  
M Messager ◽  
C Carrière ◽  
X Bertagna ◽  
Y de Keyzer

Objective: ACTH is frequently produced in non-pituitary tumours, leading to the ectopic-ACTH syndrome, but the molecular mechanisms of its expression remain obscure. This study was aimed at understanding the transcription mechanisms of the ACTH-precursor gene in carcinoid tumours of the lung or thymus. Design: Transcripts coding for a series of corticotroph-associated transcription factor genes were detected, together with markers of the corticotroph phenotype. We studied a series of 41 carcinoid tumours including 15 with proven ectopic-ACTH syndrome. Methods: Specific RT-PCR reactions were designed for each gene including alternatively spliced isoforms. Results: The markers of the corticotroph phenotype were detected in all ACTH-positive tumours. Expression of the Tpit and Pitx1 genes were not restricted to ACTH-positive tumours but were also detected in many ACTH-negative carcinoids. Only a subset of ACTH-negative tumours expressed NAK-1/Nur77, and NeuroD1 expression was detected in <50% of the tumours regardless of their secretory status. The glucocorticoid receptor alpha was detected in every tumour in contrast to its beta isoform detectable in a few tumours only. Chicken ovalbumin upstream promoter-transcription factor 1 (COUP-TF1) and peroxisome proliferator-activated receptor (PPAR) γ2 were expressed in 50% of the tumours of each group whereas PPARγ1 was expressed in almost every tumour. Conclusions: ACTH-positive carcinoids do not share a characteristic expression pattern of the corticotroph-associated transcription factor genes, suggesting that the transcriptional mechanisms of the ACTH-precursor gene differ from those in normal pituitary corticotrophs. Expression of Tpit and Pitx1 genes in most carcinoids suggests that some aspects of the pituitary corticotroph phenotype may belong to general carcinoid differentiation.


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