Literature DB >> 35416545

Two distinct males absent on the first (MOF)-containing histone acetyltransferases are involved in the epithelial-mesenchymal transition in different ways in human cells.

Tao Wei1,2, Hongsen Liu1, Huihui Zhu1,2, Wenqi Chen1, Tingting Wu1, Yuerong Bai1, Xueyan Zhang1, Yujuan Miao1, Fei Wang1, Yong Cai3,4,5,6, Jingji Jin7,8,9.   

Abstract

Human males absent on the first (MOF), a histone acetyltransferase (HAT), forms male-specific lethal (MSL) and non-specific lethal (NSL), two multiprotein HATs, in cells. MSL was originally discovered in dosage compensation study in Drosophila that can specifically acetylate H4K16, while NSL can simultaneously catalyze the H4 at K5, K8, and K16 sites. However, comparative studies of the two HATs in regulating specific biological functions are rarely reported. Here, we present evidence to argue that MSL and NSL function in different ways in the epithelial-to-mesenchymal transition (EMT) process. At first, CRISPR/Cas9-mediated MSL1 (a key subunit of the MSL)-knockout (KO) and NSL3 (a key subunit of the NSL)-KO cells seem to prefer to grow in clusters. Interestingly, the former promotes cell survival and clonal formation, while the latter has the opposite effect on it. Cell staining revealed that MSL1-KO leads to multipolarized spindles, while NSL3-KO causes more lumen-like cells. Furthermore, in Transwell experiments, silencing of MSL1 promotes cell invasion in 293 T, MCF-7, and MDA-MB-231 cells. In contrast, the inhibitory effects on cell invasion are observed in the same NSL3-silenced cells. Consistent with this, mesenchymal biomarkers, like N-cadherin, vimentin, and snail, are negatively correlated with the expression level of MSL1; however, a positive relationship between these proteins and NSL3 in cells has been found. Further studies have clarified that MSL1, but not NSL3, can specifically bind to the E-box-containing Snail promoter region and thereby negatively regulate Snail transactivation. Also, silencing of MSL1 promotes the lung metastasis of B16F10 melanoma cells in mice. Finally, ChIP-Seq analysis indicated that the NSL may be mainly involved in phosphoinositide-mediated signaling pathways. Taken together, the MOF-containing MSL and NSL HATs may regulate the EMT process in different ways in order to respond to different stimuli.
© 2022. The Author(s), under exclusive licence to Springer Nature Switzerland AG.

Entities:  

Keywords:  Epithelial-to-mesenchymal transition; Histone acetyltransferase; Male-specific lethal; Non-specific lethal

Mesh:

Substances:

Year:  2022        PMID: 35416545     DOI: 10.1007/s00018-022-04258-6

Source DB:  PubMed          Journal:  Cell Mol Life Sci        ISSN: 1420-682X            Impact factor:   9.207


  43 in total

1.  Activation of transcription through histone H4 acetylation by MOF, an acetyltransferase essential for dosage compensation in Drosophila.

Authors:  A Akhtar; P B Becker
Journal:  Mol Cell       Date:  2000-02       Impact factor: 17.970

2.  The drosophila MSL complex acetylates histone H4 at lysine 16, a chromatin modification linked to dosage compensation.

Authors:  E R Smith; A Pannuti; W Gu; A Steurnagel; R G Cook; C D Allis; J C Lucchesi
Journal:  Mol Cell Biol       Date:  2000-01       Impact factor: 4.272

Review 3.  roX RNAs: non-coding regulators of the male X chromosome in flies.

Authors:  Ibrahim Ilik; Asifa Akhtar
Journal:  RNA Biol       Date:  2009-04-03       Impact factor: 4.652

Review 4.  The MSL complex: juggling RNA-protein interactions for dosage compensation and beyond.

Authors:  Claudia Isabelle Keller; Asifa Akhtar
Journal:  Curr Opin Genet Dev       Date:  2015-04-19       Impact factor: 5.578

5.  Studies on the sex-specific lethals of Drosophila melanogaster. II. Further studies on a male-specific lethal gene, maleless.

Authors:  A Tanaka; A Fukunaga; K Oishi
Journal:  Genetics       Date:  1976-10       Impact factor: 4.562

6.  Structural basis for MOF and MSL3 recruitment into the dosage compensation complex by MSL1.

Authors:  Jan Kadlec; Erinc Hallacli; Michael Lipp; Herbert Holz; Juan Sanchez-Weatherby; Stephen Cusack; Asifa Akhtar
Journal:  Nat Struct Mol Biol       Date:  2011-01-09       Impact factor: 15.369

7.  Subunit composition and substrate specificity of a MOF-containing histone acetyltransferase distinct from the male-specific lethal (MSL) complex.

Authors:  Yong Cai; Jingji Jin; Selene K Swanson; Michael D Cole; Seung Hyuk Choi; Laurence Florens; Michael P Washburn; Joan W Conaway; Ronald C Conaway
Journal:  J Biol Chem       Date:  2009-12-14       Impact factor: 5.157

8.  hMOF, a KAT(8) with many lives.

Authors:  Hestia S Mellert; Steven B McMahon
Journal:  Mol Cell       Date:  2009-10-23       Impact factor: 17.970

Review 9.  Males absent on the first (MOF): from flies to humans.

Authors:  S Rea; G Xouri; A Akhtar
Journal:  Oncogene       Date:  2007-08-13       Impact factor: 9.867

10.  Msl1-mediated dimerization of the dosage compensation complex is essential for male X-chromosome regulation in Drosophila.

Authors:  Erinc Hallacli; Michael Lipp; Plamen Georgiev; Clare Spielman; Stephen Cusack; Asifa Akhtar; Jan Kadlec
Journal:  Mol Cell       Date:  2012-10-18       Impact factor: 17.970

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