洞察 - Developmental biology - # Regulation of the first cell-fate decision by asymmetric HSPA2 expression in mouse embryos

The Asymmetric Expression of Heat Shock Protein A2 (HSPA2) Regulates the First Cell-Fate Decision in Mouse Embryos

Q: How do the asymmetric distribution patterns of HSPA2 and CARM1 arise in early embryos, and what are the upstream regulators controlling this heterogeneity?

The asymmetric distribution patterns of HSPA2 and CARM1 in early embryos, particularly during the late 2-cell stage, are likely influenced by several factors. The study indicates that HSPA2 exhibits a heterogeneous expression pattern that correlates with the expression of ICM-specific genes, suggesting that its distribution is not random but rather regulated. The emergence of this asymmetry may be traced back to the processes occurring during zygotic genome activation (ZGA), where maternal factors and the newly transcribed zygotic genes begin to influence embryonic development. Upstream regulators of this heterogeneity could include maternal mRNAs and proteins that are asymmetrically localized within the oocyte and early embryo. For instance, the presence of long non-coding RNAs, such as LincGET, has been shown to exhibit asymmetric expression in early embryos and may interact with CARM1 to promote the differential methylation of histones, specifically H3R26me. This methylation is crucial for activating ICM-specific gene expression. Additionally, the spatial distribution of other signaling molecules and transcription factors, such as PRDM14, may also contribute to the establishment of this molecular heterogeneity, ultimately guiding the first cell-fate decision.

Q: What other molecular pathways or signaling cascades might be influenced by the HSPA2-CARM1 interaction to govern cell fate decisions?

The interaction between HSPA2 and CARM1 is pivotal in regulating cell fate decisions, particularly through the modification of histones, such as H3R26me2, which is associated with the activation of ICM-specific genes. Beyond this direct interaction, several other molecular pathways and signaling cascades may be influenced by the HSPA2-CARM1 complex. Wnt Signaling Pathway: The Wnt pathway is known to play a significant role in cell proliferation, differentiation, and fate determination during embryonic development. The HSPA2-CARM1 interaction may modulate Wnt signaling by regulating the expression of Wnt target genes, thereby influencing the balance between ICM and TE cell fates. Hippo Signaling Pathway: The Hippo pathway is crucial for controlling cell growth and regulating the balance between ICM and TE cell fates. HSPA2 may impact the expression of Hippo pathway components, thereby affecting the signaling that determines cell lineage specification. Notch Signaling: Notch signaling is another pathway that influences cell fate decisions. The HSPA2-CARM1 complex could potentially interact with Notch pathway components, modulating their activity and thus affecting the differentiation of blastomeres. Cell Cycle Regulation: Given that HSPA2 is involved in cell cycle progression, its interaction with CARM1 may also influence pathways that regulate the cell cycle, thereby linking cell proliferation with lineage specification. Overall, the HSPA2-CARM1 interaction likely serves as a nexus for multiple signaling pathways that collectively govern the complex process of cell fate determination in early embryonic development.

核心概念

The molecular chaperone HSPA2 exhibits asymmetric expression in late 2-cell and 4-cell stage mouse embryos, and its differential distribution governs the first cell-fate decision by regulating ICM-specific gene expression through interaction with CARM1.

摘要

The study investigates the role of the molecular chaperone HSPA2 in the first cell-fate decision during early mouse embryonic development. Key findings:

HSPA2 is asymmetrically expressed in late 2-cell and 4-cell stage mouse embryos, with distinct mRNA and protein levels among the blastomeres.
Knockdown of Hspa2 in one blastomere of 2-cell embryos leads to reduced expression of ICM-specific genes (Oct4, Sox2, Nanog) and decreased contribution of that blastomere's progeny to the inner cell mass (ICM) at the blastocyst stage.
Overexpression of Hspa2 does not induce bias towards the ICM fate.
HSPA2 physically interacts with the histone methyltransferase CARM1 and regulates the levels of H3R26me2, a histone modification associated with ICM specification.
Hspa2 knockdown results in reduced CARM1 expression, suggesting HSPA2 acts upstream of CARM1 to control ICM lineage establishment.

The findings demonstrate that the asymmetric distribution of HSPA2 in early embryos is a critical regulator of the first cell-fate decision, directing blastomeres towards the ICM or trophectoderm lineages through its interaction with CARM1 and modulation of histone modifications.

自定义摘要

使用 AI 改写

生成参考文献

翻译原文

翻译成其他语言

生成思维导图

从原文生成

访问来源

biorxiv.org

统计

The blastocyst formation rate in the Hspa2-knockdown group (52.96±2.489%) was significantly lower than that in the control group (81.63±2.000%).
The number of ICM cells and total cells in the blastocyst were significantly decreased in the Hspa2-knockdown group compared to the control.
Hspa2 knockdown led to a dramatic decrease in H3R26me2 modification at the 4-cell stage.

引用

"The knockdown of Hspa2 in one of the two-cell blastomeres prevented its progeny predominantly toward the inner cell mass (ICM) fate, thus indicating that the differential distribution of HSPA2 in the blastomeres of two-cell embryos can influence the selection of embryonic cell lineages."
"HSPA2 forms a complex with CARM1 and activates ICM-specific gene expression."

从中提取的关键见解

The asymmetric expression of HSPA2 in blastomeres governs the first embryonic cell-fate decision

by Gao,J., Wang... 在 www.biorxiv.org 07-19-2024

https://www.biorxiv.org/content/10.1101/2024.07.16.603746v1

更深入的查询

How do the asymmetric distribution patterns of HSPA2 and CARM1 arise in early embryos, and what are the upstream regulators controlling this heterogeneity?

The asymmetric distribution patterns of HSPA2 and CARM1 in early embryos, particularly during the late 2-cell stage, are likely influenced by several factors. The study indicates that HSPA2 exhibits a heterogeneous expression pattern that correlates with the expression of ICM-specific genes, suggesting that its distribution is not random but rather regulated. The emergence of this asymmetry may be traced back to the processes occurring during zygotic genome activation (ZGA), where maternal factors and the newly transcribed zygotic genes begin to influence embryonic development.
Upstream regulators of this heterogeneity could include maternal mRNAs and proteins that are asymmetrically localized within the oocyte and early embryo. For instance, the presence of long non-coding RNAs, such as LincGET, has been shown to exhibit asymmetric expression in early embryos and may interact with CARM1 to promote the differential methylation of histones, specifically H3R26me. This methylation is crucial for activating ICM-specific gene expression. Additionally, the spatial distribution of other signaling molecules and transcription factors, such as PRDM14, may also contribute to the establishment of this molecular heterogeneity, ultimately guiding the first cell-fate decision.

What other molecular pathways or signaling cascades might be influenced by the HSPA2-CARM1 interaction to govern cell fate decisions?

The interaction between HSPA2 and CARM1 is pivotal in regulating cell fate decisions, particularly through the modification of histones, such as H3R26me2, which is associated with the activation of ICM-specific genes. Beyond this direct interaction, several other molecular pathways and signaling cascades may be influenced by the HSPA2-CARM1 complex.

Wnt Signaling Pathway: The Wnt pathway is known to play a significant role in cell proliferation, differentiation, and fate determination during embryonic development. The HSPA2-CARM1 interaction may modulate Wnt signaling by regulating the expression of Wnt target genes, thereby influencing the balance between ICM and TE cell fates.

Hippo Signaling Pathway: The Hippo pathway is crucial for controlling cell growth and regulating the balance between ICM and TE cell fates. HSPA2 may impact the expression of Hippo pathway components, thereby affecting the signaling that determines cell lineage specification.

Notch Signaling: Notch signaling is another pathway that influences cell fate decisions. The HSPA2-CARM1 complex could potentially interact with Notch pathway components, modulating their activity and thus affecting the differentiation of blastomeres.

Cell Cycle Regulation: Given that HSPA2 is involved in cell cycle progression, its interaction with CARM1 may also influence pathways that regulate the cell cycle, thereby linking cell proliferation with lineage specification.

Overall, the HSPA2-CARM1 interaction likely serves as a nexus for multiple signaling pathways that collectively govern the complex process of cell fate determination in early embryonic development.

Given the role of HSPA2 in regulating cell cycle progression, how might its effects on proliferation versus lineage specification be mechanistically linked during the first cell-fate decision?

HSPA2 plays a dual role in regulating both cell cycle progression and lineage specification, particularly during the first cell-fate decision in early embryonic development. The mechanistic link between these two processes can be understood through several interconnected pathways and regulatory mechanisms.

Cell Cycle Regulation: HSPA2 has been shown to influence cell cycle dynamics, particularly by promoting cell proliferation. In the context of early embryonic development, the timing and regulation of cell division are critical for ensuring that the correct number of cells is allocated to the ICM and TE lineages. If HSPA2 is downregulated, as observed in the study, it leads to reduced cell proliferation and a subsequent decrease in the number of ICM cells, indicating that HSPA2 is essential for maintaining the appropriate cell cycle progression necessary for lineage specification.

G1/S Transition: The study highlights that HSPA2 knockdown results in G1/S phase cell cycle arrest. This arrest can prevent cells from progressing through the cell cycle, thereby limiting the number of cells that can contribute to the ICM. This suggests that HSPA2 not only promotes proliferation but also ensures that cells are adequately prepared to undergo differentiation into specific lineages.

Histone Modification and Gene Expression: HSPA2's interaction with CARM1 and the subsequent modification of histones (e.g., H3R26me2) are crucial for activating ICM-specific gene expression. This histone modification is linked to transcriptional activation, which is necessary for the expression of genes that drive lineage specification. Thus, HSPA2's role in promoting cell cycle progression is coupled with its function in regulating gene expression, creating a feedback loop where proliferation supports lineage specification.

Balancing Proliferation and Differentiation: The balance between proliferation and differentiation is a hallmark of early embryonic development. HSPA2 may help maintain this balance by ensuring that while cells proliferate, they also receive the necessary signals to differentiate into the appropriate lineages. This is particularly important during the first cell-fate decision, where the correct allocation of cells to the ICM and TE is essential for successful embryonic development.

In summary, HSPA2 serves as a critical regulator that links cell cycle progression with lineage specification, ensuring that the early embryonic cells can both proliferate and differentiate appropriately during the first cell-fate decision.