What are the main pathways to synthesise lipid species in human cells?5 answersThe main pathways for synthesizing lipid species in human cells involve the biosynthesis of phospholipids through various mechanisms. Phospholipids, essential components of cell membranes, are synthesized de novo primarily in the endoplasmic reticulum, utilizing precursors like DAG, CDP-DAG, choline, ethanolamine, inositol, and glycerol. Enzymatic methods, including the CDP-choline and methylation pathways, are crucial for phosphatidylcholine synthesis, while phosphatidylethanolamine biosynthesis occurs via the CDP-ethanolamine and phosphatidylserine decarboxylase pathways. Human embryonic fibroblasts synthesize phospholipids by utilizing glycerol from glycolysis, fatty acids, and base precursors like phosphatidyl ethanolamine, which can be methylated to form phosphatidylcholine. The synthesis of novel phospholipid species, such as cardiolipins and bis(mono/di-acylglycero)phosphates, is also significant for various health benefits and applications.
How is the rate of branched-chain fatty acid biosynthesis regulated in plants?5 answersThe rate of branched-chain fatty acid biosynthesis in plants is regulated through a combination of transcriptional control and enzymatic modifications. Transcriptional regulation plays a crucial role in modulating the rate of fatty acid production, with the WRINKLED1 transcription factor being identified as an important regulator. Enzymatic modifications, such as covalent and allosteric modifications, regulate the carboxylation of acetyl-CoA, which is the precursor for fatty acid biosynthesis. Additionally, the length of the acyl chains and the degree of unsaturation are regulated by thioesterases, elongases, and desaturases. These enzymatic processes contribute to the structural diversity of fatty acids. Overall, the regulation of branched-chain fatty acid biosynthesis involves a complex interplay between transcriptional control and enzymatic modifications to ensure that the supply of fatty acids matches the demand in different cell types.
Is there an acetyl CoA production pathway from allantoin?5 answersThere is no mention of an acetyl CoA production pathway from allantoin in the provided abstracts.
How dose fatty acid oxidation affect gene expression?5 answersFatty acid oxidation has a significant impact on gene expression. Fatty acids and their metabolites can modulate the activity of nuclear transcription factors, such as peroxisome proliferator-activated receptors (PPARs) and sterol regulatory element binding protein type 1 (SREBP-1). These transcription factors play crucial roles in regulating the expression of genes involved in various cellular functions, including proliferation, differentiation, and metabolism. Fatty acids can affect the expression of key enzymes involved in fatty acid oxidation, such as long-chain acyl-coenzyme A synthetase, carnitine palmitoyltransferase I, and long-chain acyl-coenzyme A dehydrogenase. The upregulation of these enzymes is associated with an overall shift from glucose to fatty acids as the preferred fuel for mitochondrial ATP production. The regulation of gene expression by fatty acid oxidation is complex and involves multiple nutrient- and energy-sensitive molecular mechanisms. These findings highlight the important role of fatty acid oxidation in the control of gene expression and cellular metabolism.
How dose lipid metabolism affect gene expression?5 answersLipid metabolism plays a significant role in regulating gene expression. Lipids and their metabolites are involved in lipid-gene interactions, which impact nuclear functions, chromatin architecture, gene expression, and transcription. Lipid-derived acetyl-CoA, derived from fatty acids, is a major carbon source for histone acetylation, a process that controls gene expression. Transcription factors such as peroxisome proliferator-activated receptor (PPAR) and carbohydrate response element binding protein (ChREBP) are activated by lipids and carbohydrates, respectively, and play a crucial role in metabolic homeostasis, including glucose and lipid metabolism. Lipid metabolism genes, including APOE, APOC1, and GLUL, are highly expressed in the central nervous system (CNS) and are implicated in neuroprotection and neurodegeneration. Furthermore, lipid metabolism, particularly cholesterol metabolism and arachidonic acid metabolism, may be involved in the pathogenesis of certain diseases, such as idiopathic membranous nephropathy, through the regulation of specific genes.
What is the function DHCR24 gene in lipid metabolism?2 answersThe DHCR24 gene is involved in lipid metabolism. It encodes an enzyme called 3β-hydroxysterol-Δ24 reductase, which plays a key role in the cholesterologenic pathway. DHCR24 is responsible for converting desmosterol into cholesterol, and its expression is crucial for proper skin development and function. In addition, DHCR24 has been associated with altered microstructural properties of white matter in adolescents, suggesting a link between peripheral metabolism and brain microstructure. The gene has also been implicated in endometrial cancer, where its up-regulation is associated with advanced disease and reduced overall survival. While the exact mechanisms are still being investigated, DHCR24 appears to have a multifaceted role in lipid metabolism and may have implications for cognitive impairment and cancer progression.