Evidence map›Paper›PMID 35416545›Full record

ArticleCellular and molecular life sciences : CMLS2022

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 Wei, Hongsen Liu, Huihui Zhu, Wenqi Chen, Tingting Wu, Yuerong Bai, Xueyan Zhang, Yujuan Miao, Fei Wang, Yong Cai and 1 more

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 15 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 1 institution in 2 countries.

Tao WeiSchool of Life Sciences, Jilin University, Changchun, 130012, China.
Hongsen LiuSchool of Life Sciences, Jilin University, Changchun, 130012, China.
Huihui ZhuSchool of Life Sciences, Jilin University, Changchun, 130012, China.
Wenqi ChenSchool of Life Sciences, Jilin University, Changchun, 130012, China.
Tingting WuSchool of Life Sciences, Jilin University, Changchun, 130012, China.
Yuerong BaiSchool of Life Sciences, Jilin University, Changchun, 130012, China.
Xueyan ZhangSchool of Life Sciences, Jilin University, Changchun, 130012, China.
Yujuan MiaoSchool of Life Sciences, Jilin University, Changchun, 130012, China.
Fei WangSchool of Life Sciences, Jilin University, Changchun, 130012, China.
Yong CaiSchool of Life Sciences, Jilin University, Changchun, 130012, China. caiyong62@jlu.edu.cn.
Jingji JinSchool of Life Sciences, Jilin University, Changchun, 130012, China. jjjin@jlu.edu.cn.ORCID http://orcid.org/0000-0001-9432-5954
Jilin University · CN

Funding

National Natural Science Foundation of China No. 31771421National Natural Science Foundation of China No. 32170599
6 · The paper itself

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.

Indexed as

Epithelial-Mesenchymal TransitionHistone AcetyltransferasesAcetylationAnimalsDosage Compensation, GeneticHumansMiceHistone AcetyltransferasesKAT8 protein, humanEpithelial-to-mesenchymal transitionHistone acetyltransferaseMale-specific lethalNon-specific lethal

Identifiers

PMID35416545
PMCPMC11073432
OpenAlexW4223414657

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.