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  1. Article ; Online: MLL regulates the actin cytoskeleton and cell migration by stabilising Rho GTPases via the expression of RhoGDI1.

    Chinchole, Akash / Lone, Kaisar Ahmad / Tyagi, Shweta

    Journal of cell science

    2022  Volume 135, Issue 20

    Abstract: Attainment of proper cell shape and the regulation of cell migration are essential processes in the development of an organism. The mixed lineage leukemia (MLL or KMT2A) protein, a histone 3 lysine 4 (H3K4) methyltransferase, plays a critical role in ... ...

    Abstract Attainment of proper cell shape and the regulation of cell migration are essential processes in the development of an organism. The mixed lineage leukemia (MLL or KMT2A) protein, a histone 3 lysine 4 (H3K4) methyltransferase, plays a critical role in cell-fate decisions during skeletal development and haematopoiesis in higher vertebrates. Rho GTPases - RhoA, Rac1 and CDC42 - are small G proteins that regulate various key cellular processes, such as actin cytoskeleton formation, the maintenance of cell shape and cell migration. Here, we report that MLL regulates the homeostasis of these small Rho GTPases. Loss of MLL resulted in an abnormal cell shape and a disrupted actin cytoskeleton, which lead to diminished cell spreading and migration. MLL depletion affected the stability and activity of Rho GTPases in a SET domain-dependent manner, but these Rho GTPases were not direct transcriptional targets of MLL. Instead, MLL regulated the transcript levels of their chaperone protein RhoGDI1 (also known as ARHGDIA). Using MDA-MB-231, a triple-negative breast cancer cell line with high RhoGDI1 expression, we show that MLL depletion or inhibition by small molecules reduces tumour progression in nude mice. Our studies highlight the central regulatory role of MLL in Rho/Rac/CDC42 signalling pathways. This article has an associated First Person interview with the first author of the paper.
    MeSH term(s) Mice ; Animals ; rho Guanine Nucleotide Dissociation Inhibitor alpha/genetics ; rho Guanine Nucleotide Dissociation Inhibitor alpha/metabolism ; rho GTP-Binding Proteins/genetics ; rho GTP-Binding Proteins/metabolism ; Mice, Nude ; Histones/metabolism ; Lysine ; Signal Transduction/physiology ; cdc42 GTP-Binding Protein/genetics ; cdc42 GTP-Binding Protein/metabolism ; rhoA GTP-Binding Protein/genetics ; rhoA GTP-Binding Protein/metabolism ; Cell Movement/physiology ; Actin Cytoskeleton/metabolism ; Methyltransferases/metabolism ; rac1 GTP-Binding Protein/metabolism ; Actins/metabolism
    Chemical Substances rho Guanine Nucleotide Dissociation Inhibitor alpha ; rho GTP-Binding Proteins (EC 3.6.5.2) ; Histones ; Lysine (K3Z4F929H6) ; cdc42 GTP-Binding Protein (EC 3.6.5.2) ; rhoA GTP-Binding Protein (EC 3.6.5.2) ; Methyltransferases (EC 2.1.1.-) ; rac1 GTP-Binding Protein (EC 3.6.5.2) ; Actins
    Language English
    Publishing date 2022-10-20
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2993-2
    ISSN 1477-9137 ; 0021-9533
    ISSN (online) 1477-9137
    ISSN 0021-9533
    DOI 10.1242/jcs.260042
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Genotype first approach & familial segregation analysis help in the elucidation of disease-causing variant for fucosidosis.

    Bhattacherjee, Amrita / Desa, Elyska / Lone, Kaisar Ahmad / Jaiswal, Arjita / Tyagi, Shweta / Dalal, Ashwin

    The Indian journal of medical research

    2023  Volume 157, Issue 4, Page(s) 363–366

    MeSH term(s) Humans ; Fucosidosis/genetics ; Genotype
    Language English
    Publishing date 2023-06-09
    Publishing country India
    Document type Journal Article
    ZDB-ID 390883-5
    ISSN 0971-5916 ; 0019-5340
    ISSN 0971-5916 ; 0019-5340
    DOI 10.4103/ijmr.IJMR_3568_20
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: MLL methyltransferases regulate H3K4 methylation to ensure CENP-A assembly at human centromeres.

    Malik, Kausika Kumar / Sridhara, Sreerama Chaitanya / Lone, Kaisar Ahmad / Katariya, Payal Deepakbhai / Pulimamidi, Deepshika / Tyagi, Shweta

    PLoS biology

    2023  Volume 21, Issue 6, Page(s) e3002161

    Abstract: The active state of centromeres is epigenetically defined by the presence of CENP-A interspersed with histone H3 nucleosomes. While the importance of dimethylation of H3K4 for centromeric transcription has been highlighted in various studies, the ... ...

    Abstract The active state of centromeres is epigenetically defined by the presence of CENP-A interspersed with histone H3 nucleosomes. While the importance of dimethylation of H3K4 for centromeric transcription has been highlighted in various studies, the identity of the enzyme(s) depositing these marks on the centromere is still unknown. The MLL (KMT2) family plays a crucial role in RNA polymerase II (Pol II)-mediated gene regulation by methylating H3K4. Here, we report that MLL methyltransferases regulate transcription of human centromeres. CRISPR-mediated down-regulation of MLL causes loss of H3K4me2, resulting in an altered epigenetic chromatin state of the centromeres. Intriguingly, our results reveal that loss of MLL, but not SETD1A, increases co-transcriptional R-loop formation, and Pol II accumulation at the centromeres. Finally, we report that the presence of MLL and SETD1A is crucial for kinetochore maintenance. Altogether, our data reveal a novel molecular framework where both the H3K4 methylation mark and the methyltransferases regulate stability and identity of the centromere.
    MeSH term(s) Humans ; Autoantigens/metabolism ; Centromere/metabolism ; Centromere Protein A/genetics ; Centromere Protein A/metabolism ; Chromatin ; Chromosomal Proteins, Non-Histone/genetics ; Chromosomal Proteins, Non-Histone/metabolism ; Methylation ; Methyltransferases/genetics ; Nucleosomes
    Chemical Substances Autoantigens ; Centromere Protein A ; Chromatin ; Chromosomal Proteins, Non-Histone ; Methyltransferases (EC 2.1.1.-) ; Nucleosomes ; CENPA protein, human ; KMT2A protein, human
    Language English
    Publishing date 2023-06-28
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2126776-5
    ISSN 1545-7885 ; 1544-9173
    ISSN (online) 1545-7885
    ISSN 1544-9173
    DOI 10.1371/journal.pbio.3002161
    Database MEDical Literature Analysis and Retrieval System OnLINE

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