scholarly journals Mammalian E4 Is Required for Cardiac Development and Maintenance of the Nervous System

2005 ◽  
Vol 25 (24) ◽  
pp. 10953-10964 ◽  
Author(s):  
Chie Kaneko-Oshikawa ◽  
Tadashi Nakagawa ◽  
Mitsunori Yamada ◽  
Hiroo Yoshikawa ◽  
Masaki Matsumoto ◽  
...  

ABSTRACT Ubiquitin conjugation typically requires three classes of enzyme: E1, E2, and E3. A fourth type of enzyme (E4), however, was recently shown to be required for the degradation of certain types of substrate in yeast. We previously identified UFD2a (also known as E4B) as an E4 in mammals. UFD2a is exclusively expressed in cardiac muscle during mouse embryonic development, but it is abundant in neurons of adult mice and is implicated in the pathogenesis of neurodegenerative disease. The precise physiological function of this enzyme has remained largely unknown, however. Here, we show that mice lacking UFD2a die in utero, manifesting marked apoptosis in the developing heart. Polyubiquitylation activity for an E4 substrate was greatly reduced in Ufd2a −/− mouse embryonic fibroblasts. Furthermore, Ufd2a +/− mice displayed axonal dystrophy in the nucleus gracilis, as well as degeneration of Purkinje cells accompanied by endoplasmic reticulum stress. These animals also developed a neurological disorder. UFD2a thus appears to be essential for the development of cardiac muscle, as well as for the protection of spinocerebellar neurons from degeneration induced by endoplasmic reticulum stress.

2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Keiko Muramatsu-Kato ◽  
Hiroaki Itoh ◽  
Yukiko Kohmura-Kobayashi ◽  
Urmi J. Ferdous ◽  
Naoaki Tamura ◽  
...  

2007 ◽  
Vol 282 (19) ◽  
pp. 14132-14139 ◽  
Author(s):  
Ali Masud ◽  
Alexander Mohapatra ◽  
Saquib A. Lakhani ◽  
Anthony Ferrandino ◽  
Razqallah Hakem ◽  
...  

2018 ◽  
Vol 26 ◽  
pp. S81
Author(s):  
K.L. Posey ◽  
F. Chiu ◽  
A. Veerisetty ◽  
J.L. Alcorn ◽  
J.T. Hecht

2018 ◽  
Vol 356 ◽  
pp. 172-181 ◽  
Author(s):  
Yongchao Wang ◽  
Xin Wang ◽  
Hui Li ◽  
Mei Xu ◽  
Jacqueline Frank ◽  
...  

2008 ◽  
Vol 2 (1) ◽  
pp. 31-35 ◽  
Author(s):  
Sylvia Papp ◽  
Xiaochu Zhang ◽  
Eva Szabo ◽  
Marek Michalak ◽  
Michal Opas

To determine if cardiogenesis causes endoplasmic reticulum stress, we examined chaperone expression. Many cardiac pathologies cause activation of the fetal gene program, and we asked the reverse: could activation of the fetal gene program during development induce endoplasmic reticulum stress/chaperones? We found stress related chaperones were more abundant in embryonic compared to adult hearts, indicating endoplasmic reticulum stress during normal cardiac development. To determine the degree of stress, we investigated endoplasmic reticulum stress pathways during cardiogenesis. We detected higher levels of ATF6α, caspase 7 and 12 in adult hearts. Thus, during embryonic development, there is large protein synthetic load but there is no endoplasmic reticulum stress. In adult hearts, chaperones are less abundant but there are increased levels of ATF6α and ER stress-activated caspases. Thus, protein synthesis during embryonic development does not seem to be as intense a stress as is required for apoptosis that is found during postnatal remodelling.


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