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1.
Plant Cell ; 34(10): 3557-3576, 2022 09 27.
Artigo em Inglês | MEDLINE | ID: mdl-35849348

RESUMO

The copy numbers of many plant transcription factor (TF) genes substantially increased during terrestrialization. This allowed TFs to acquire new specificities and thus create gene regulatory networks (GRNs) with new biological functions to help plants adapt to terrestrial environments. Through characterizing heat shock factor (HSF) genes MpHSFA1 and MpHSFB1 in the liverwort Marchantia polymorpha, we explored how heat-responsive GRNs widened their functions in M. polymorpha and Arabidopsis thaliana. An interspecies comparison of heat-induced transcriptomes and the evolutionary rates of HSFs demonstrated the emergence and subsequent rapid evolution of HSFB prior to terrestrialization. Transcriptome and metabolome analyses of M. polymorpha HSF-null mutants revealed that MpHSFA1 controls canonical heat responses such as thermotolerance and metabolic changes. MpHSFB1 also plays essential roles in heat responses, as well as regulating developmental processes including meristem branching and antheridiophore formation. Analysis of cis-regulatory elements revealed development- and stress-related TFs that function directly or indirectly downstream of HSFB. Male gametophytes of M. polymorpha showed higher levels of thermotolerance than female gametophytes, which could be explained by different expression levels of MpHSFA1U and MpHSFA1V on sex chromosome. We propose that the diversification of HSFs is linked to the expansion of HS responses, which enabled coordinated multicellular reactions in land plants.


Assuntos
Arabidopsis , Marchantia , Arabidopsis/metabolismo , Regulação da Expressão Gênica de Plantas/genética , Redes Reguladoras de Genes , Fatores de Transcrição de Choque Térmico/metabolismo , Resposta ao Choque Térmico/genética , Marchantia/genética , Marchantia/metabolismo , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo
2.
Cell Rep ; 43(8): 114592, 2024 Aug 27.
Artigo em Inglês | MEDLINE | ID: mdl-39110593

RESUMO

Vesicle-associated membrane protein (VAMP)-associated proteins (VAPs) are highly conserved endoplasmic reticulum (ER)-resident proteins that establish ER contacts with multiple membrane compartments in many eukaryotes. However, VAP-mediated membrane-tethering mechanisms remain ambiguous. Here, focusing on fission yeast ER-plasma membrane (PM) contact formation, using systematic interactome analyses and quantitative microscopy, we predict a non-VAP-protein direct binding-based ER-PM coupling. We further reveal that VAP-anionic phospholipid interactions may underlie ER-PM association and define the pH-responsive nature of VAP-tethered membrane contacts. Such conserved interactions with anionic phospholipids are generally defective in amyotrophic lateral sclerosis-associated human VAPB mutant. Moreover, we identify a conserved FFAT-like motif locating at the autoinhibitory hotspot of the essential PM proton pump Pma1. This modulatory VAP-Pma1 interaction appears crucial for pH homeostasis. We thus propose an ingenious strategy for maintaining intracellular pH by coupling Pma1 modulation with pH-sensory ER-PM contacts via VAP-mediated interactions.


Assuntos
Membrana Celular , Retículo Endoplasmático , Homeostase , Schizosaccharomyces , Retículo Endoplasmático/metabolismo , Concentração de Íons de Hidrogênio , Membrana Celular/metabolismo , Humanos , Schizosaccharomyces/metabolismo , Proteínas de Schizosaccharomyces pombe/metabolismo , Proteínas de Transporte Vesicular/metabolismo , Proteínas de Transporte Vesicular/genética , Ligação Proteica , Proteínas de Membrana/metabolismo , Fosfolipídeos/metabolismo , Mutação , Esclerose Lateral Amiotrófica/metabolismo
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