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LMKB/MARF1 localizes to mRNA processing bodies, interacts with Ge-1, and regulates IFI44L gene expression
Donald B Bloch1, Pingcheng Li2, Emily G Bloch2
1Center for Immunology and Inflammatory Diseases, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, United States of America; Anesthesia Center for Critical Care Research, Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, United States of America.
Abstract:
The mRNA processing body (P-body) is a cellular structure that regulates the stability of cytoplasmic mRNA. MARF1 is a murine oocyte RNA-binding protein that is associated with maintenance of mRNA homeostasis and genomic stability. In this study, autoantibodies were used to identify Limkain B (LMKB), the human orthologue of MARF1, as a P-body component. Indirect immunofluorescence demonstrated that Ge-1 (a central component of the mammalian core-decapping complex) co-localized with LMKB in P-bodies. Two-hybrid and co-immunoprecipitation assays were used to demonstrate interaction between Ge-1 and LMKB. The C-terminal 120 amino acids of LMKB mediated interaction with Ge-1 and the N-terminal 1094 amino acids of Ge-1 were required for interaction with LMKB. LMKB is the first protein identified to date that interacts with this portion of Ge-1. LMKB was expressed in human B and T lymphocyte cell lines; depletion of LMKB increased expression of IFI44L, a gene that has been implicated in the cellular response to Type I interferons. The interaction between LMKB/MARF1, a protein that contains RNA-binding domains, and Ge-1, which interacts with core-decapping proteins, suggests that LMKB has a role in the regulation of mRNA stability. LMKB appears to have different functions in different cell types: maintenance of genomic stability in developing oocytes and possible dampening of the inflammatory response in B and T cells.
Insights
Limkain B (LMKB) is identified as a component of mRNA processing bodies (P-bodies), interacting with Ge-1 to regulate mRNA stability. LMKB plays roles in genomic stability and dampening inflammatory responses.
Area of Science:
- Cell Biology
- Molecular Biology
- Immunology
Background:
- mRNA processing bodies (P-bodies) regulate cytoplasmic mRNA stability.
- MARF1, a murine protein, is crucial for mRNA homeostasis and genomic stability.
- The function of MARF1's human orthologue, LMKB, in P-bodies was unexplored.
Purpose of the Study:
- To identify LMKB as a P-body component.
- To investigate the interaction between LMKB and Ge-1, a core-decapping complex protein.
- To elucidate the role of LMKB in mRNA regulation and cellular functions.
Main Methods:
- Autoantibodies were used to identify LMKB in P-bodies.
- Indirect immunofluorescence confirmed co-localization of LMKB and Ge-1.
- Two-hybrid and co-immunoprecipitation assays analyzed the LMKB-Ge-1 interaction.
Main Results:
- LMKB was identified as a P-body component, co-localizing with Ge-1.
- Specific domains of LMKB (C-terminal 120 amino acids) and Ge-1 (N-terminal 1094 amino acids) mediated their interaction.
- LMKB depletion in lymphocytes increased IFI44L expression, suggesting a role in interferon response.
Conclusions:
- LMKB interacts with Ge-1, implicating it in mRNA stability regulation.
- LMKB exhibits cell-type-specific functions, including genomic stability in oocytes and modulating inflammatory responses in lymphocytes.
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