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LIN-42, the Caenorhabditis elegans PERIOD homolog, Negatively

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Author Summary MicroRNAs play pervasive roles in controlling gene expression throughout animal development. Given that individual microRNAs are predicted to regulate hundreds of mRNAs and that most mRNA transcripts are microRNA targets, it is essential that the expression levels of microRNAs be tightly regulated. With the goal of unveiling factors that regulate the expression of microRNAs that control developmental timing, we identified lin-42, the C. elegans homolog of the human and Drosophila period gene implicated in circadian gene regulation, as a negative regulator of microRNA expression. By analyzing the transcriptional expression patterns of representative microRNAs, we found that the transcription of many microRNAs is normally highly dynamic and coupled aspects of post-embryonic growth and behavior. We suggest that lin-42 functions to modulate the transcriptional output of temporally-regulated microRNAs and mRNAs in order to maintain optimal expression of these genes throughout development.

lin-42 controls the output of lin-4 and let-7 transcription. (A)

PDF] Conservation of mRNA and protein expression during development of C. elegans.

Feedback between a retinoid-related nuclear receptor and the let-7 microRNAs controls the pace and number of molting cycles in C. elegans

mtDNA Leaders in Pharmaceutical Business Intelligence (LPBI) Group

Feedback between a retinoid-related nuclear receptor and the let-7 microRNAs controls the pace and number of molting cycles in C. elegans

Mutations in lin-42 suppress defects in temporal gene expression and

Age-related micro-RNA abundance in individual C. elegans

siRNA Leaders in Pharmaceutical Business Intelligence (LPBI) Group

LIN-42, the Caenorhabditis elegans PERIOD homolog, Negatively Regulates MicroRNA Transcription

In development, it's all about the timing

RNA silencing pathways in plant development and defense

The Period protein homolog LIN-42 regulates germline development in C. elegans - ScienceDirect

lin-42 mutations lead to the overexpression of several miRNAs. (A)

An Epigenetic Priming Mechanism Mediated by Nutrient Sensing Regulates Transcriptional Output during C. elegans Development. - Abstract - Europe PMC

PQN-59 antagonizes microRNA-mediated repression and functions in stress granule formation during C. elegans development

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