A hypothetical link between FAHD1 and mitochondrial resilience?

IF 0.9 Q4 GENETICS & HEREDITY
Konstantin A. Wilhelmy , Yana Rytchenko , Alexander K.H. Weiss
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引用次数: 0

Abstract

The mitochondrial enzyme FAHD1 may influence acetyl-CoA metabolism under certain conditions, although physiological relevance remains to be determined. This study explores the potential association between a naturally occurring FAHD1 variant with altered catalytic properties, that is statistically expressed in some long-lived species. Through comparative gene expression and metabolic pathway analyses in kidney, liver, and brain tissues, we examine whether this FAHD1 variant is associated with mitochondrial gene expression patterns indicative of metabolic adaptation. However, our conclusions remain exploratory and hypothesis-generating rather than definitive. The variant's altered catalytic properties might affect acetyl-CoA-related pathways, potentially influencing mitochondrial energy balance and biosynthesis, though in vivo physiological consequences remain unconfirmed. Given the exclusively transcriptomic nature of the data, no causal inferences can be drawn; the findings are exploratory and intended to generate hypotheses for future validation.
FAHD1和线粒体弹性之间的假设联系?
线粒体酶FAHD1可能在某些条件下影响乙酰辅酶a代谢,尽管生理相关性仍有待确定。本研究探讨了自然发生的FAHD1变异与催化特性改变之间的潜在关联,这在一些长寿物种中有统计学表达。通过比较肾脏、肝脏和脑组织的基因表达和代谢途径分析,我们研究了FAHD1变异是否与指示代谢适应的线粒体基因表达模式相关。然而,我们的结论仍然是探索性的和假设生成的,而不是决定性的。该变体催化特性的改变可能会影响乙酰辅酶a相关途径,潜在地影响线粒体能量平衡和生物合成,尽管体内生理后果尚未得到证实。考虑到数据的转录组学性质,无法得出因果推论;这些发现是探索性的,旨在为未来的验证产生假设。
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来源期刊
Gene Reports
Gene Reports Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.30
自引率
7.70%
发文量
246
审稿时长
49 days
期刊介绍: Gene Reports publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.
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