Changes in Gene Expression During Pancreatic Regeneration

Pancreas ◽  
1991 ◽  
Vol 6 (2) ◽  
pp. 150-156 ◽  
Author(s):  
Ezequiel L. Calvo ◽  
Nelson J. Dusetti ◽  
María B. Cadenas ◽  
Jean-Charles Dagorn ◽  
Juan L. Iovanna
Pancreas ◽  
2003 ◽  
Vol 26 (4) ◽  
pp. 368-374 ◽  
Author(s):  
Mitsuyoshi Yamamoto ◽  
Dong-Mei Jia ◽  
Ken-Ichiro Fukumitsu ◽  
Makoto Otsuki

2003 ◽  
Vol 38 (7) ◽  
pp. 672-680 ◽  
Author(s):  
Takaya Sato ◽  
Junichi Niikawa ◽  
Ichiro Usui ◽  
Tsunao Imamura ◽  
Hitoshi Yoshida ◽  
...  

Surgery ◽  
1996 ◽  
Vol 119 (5) ◽  
pp. 576-584 ◽  
Author(s):  
Michael E. Zenilman ◽  
Riccardo Perfetti ◽  
Kevin Swinson ◽  
Thomas Magnuson ◽  
Alan R. Shuldiner

Author(s):  
W. K. Jones ◽  
J. Robbins

Two myosin heavy chains (MyHC) are expressed in the mammalian heart and are differentially regulated during development. In the mouse, the α-MyHC is expressed constitutively in the atrium. At birth, the β-MyHC is downregulated and replaced by the α-MyHC, which is the sole cardiac MyHC isoform in the adult heart. We have employed transgenic and gene-targeting methodologies to study the regulation of cardiac MyHC gene expression and the functional and developmental consequences of altered α-MyHC expression in the mouse.We previously characterized an α-MyHC promoter capable of driving tissue-specific and developmentally correct expression of a CAT (chloramphenicol acetyltransferase) marker in the mouse. Tissue surveys detected a small amount of CAT activity in the lung (Fig. 1a). The results of in situ hybridization analyses indicated that the pattern of CAT transcript in the adult heart (Fig. 1b, top panel) is the same as that of α-MyHC (Fig. 1b, lower panel). The α-MyHC gene is expressed in a layer of cardiac muscle (pulmonary myocardium) associated with the pulmonary veins (Fig. 1c). These studies extend our understanding of α-MyHC expression and delimit a third cardiac compartment.


2020 ◽  
Vol 477 (16) ◽  
pp. 3091-3104 ◽  
Author(s):  
Luciana E. Giono ◽  
Alberto R. Kornblihtt

Gene expression is an intricately regulated process that is at the basis of cell differentiation, the maintenance of cell identity and the cellular responses to environmental changes. Alternative splicing, the process by which multiple functionally distinct transcripts are generated from a single gene, is one of the main mechanisms that contribute to expand the coding capacity of genomes and help explain the level of complexity achieved by higher organisms. Eukaryotic transcription is subject to multiple layers of regulation both intrinsic — such as promoter structure — and dynamic, allowing the cell to respond to internal and external signals. Similarly, alternative splicing choices are affected by all of these aspects, mainly through the regulation of transcription elongation, making it a regulatory knob on a par with the regulation of gene expression levels. This review aims to recapitulate some of the history and stepping-stones that led to the paradigms held today about transcription and splicing regulation, with major focus on transcription elongation and its effect on alternative splicing.


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