Literature DB >> 22101279

Spatio-temporal expression pattern of the NatB complex, Nat5/Mdm20 in the developing mouse brain: implications for co-operative versus non-co-operative actions of Mdm20 and Nat5.

Kyoji Ohyama1, Kunihiko Yasuda, Kazuko Onga, Akira Kakizuka, Nozomu Mori.   

Abstract

The NatB complex, Nat5/Mdm20 acetyltransferase mediates N-acetylation to control cell cycle progression and actin dynamics in yeast. As yet, little is known about the expression pattern of Mdm20 and Nat5 in multi-cellular organisms. Here we show that Mdm20 is highly expressed in mouse embryonic brain. At E11.5, Mdm20 was widely expressed in both neural progenitors and early differentiating neurons, whereas Nat5 was expressed in Sox1/3+/Mdm20+ neural progenitors. By E14.5, both Mdm20 and Nat5 were downregulated in most ventricular zone neural progenitors, whereas both proteins were found in differentiating neurons and co-expression was maintained at E18.5 in derivatives of these cells, such as midbrain dopaminergic (DA) neurons and septal neurons. These data suggest that Nat5/Mdm20 complex-mediated acetylation may play a role in the proliferation and differentiation of neural progenitors. Intriguingly, our data also showed that Mdm20 is not always co-expressed with Nat5 in all differentiated neurons, for example deep cerebellar neurons. Moreover, detailed examination of the subcellular localization of Mdm20 and Nat5 in cultured Nat5+/Mdm20+ midbrain DA neurons revealed that Mdm20 is also not necessarily co-localized with Nat5 within neurons. Given that Nat5 is only a known member of Nat family protein that interacts with Mdm20, our data imply that Mdm20 may function either with an unidentified Nat protein partner(s) or possibly in a Nat-independent manner.
Copyright © 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 22101279     DOI: 10.1016/j.gep.2011.11.001

Source DB:  PubMed          Journal:  Gene Expr Patterns        ISSN: 1567-133X            Impact factor:   1.224


  5 in total

Review 1.  The biological functions of Naa10 - From amino-terminal acetylation to human disease.

Authors:  Max J Dörfel; Gholson J Lyon
Journal:  Gene       Date:  2015-05-16       Impact factor: 3.688

2.  Mdm20 stimulates polyQ aggregation via inhibiting autophagy through Akt-Ser473 phosphorylation.

Authors:  Kunihiko Yasuda; Kyoji Ohyama; Kazuko Onga; Akira Kakizuka; Nozomu Mori
Journal:  PLoS One       Date:  2013-12-16       Impact factor: 3.240

3.  Molecular basis for N-terminal alpha-synuclein acetylation by human NatB.

Authors:  Sunbin Deng; Buyan Pan; Leah Gottlieb; E James Petersson; Ronen Marmorstein
Journal:  Elife       Date:  2020-09-04       Impact factor: 8.140

4.  Structural basis of Naa20 activity towards a canonical NatB substrate.

Authors:  Dominik Layer; Jürgen Kopp; Miriam Fontanillo; Maja Köhn; Karine Lapouge; Irmgard Sinning
Journal:  Commun Biol       Date:  2021-01-04

5.  Mdm20 Modulates Actin Remodeling through the mTORC2 Pathway via Its Effect on Rictor Expression.

Authors:  Kunihiko Yasuda; Mayumi Takahashi; Nozomu Mori
Journal:  PLoS One       Date:  2015-11-23       Impact factor: 3.240

  5 in total

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