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Open AccessJournal ArticleDOI

Genetic compensation: A phenomenon in search of mechanisms.

TLDR
This review revisits studies reporting genetic compensation in higher eukaryotes and outlines possible molecular mechanisms, which may include both transcriptional and posttranscriptional processes.
Abstract
Several recent studies in a number of model systems including zebrafish, Arabidopsis, and mouse have revealed phenotypic differences between knockouts (i.e., mutants) and knockdowns (e.g., antisense-treated animals). These differences have been attributed to a number of reasons including off-target effects of the antisense reagents. An alternative explanation was recently proposed based on a zebrafish study reporting that genetic compensation was observed in egfl7 mutant but not knockdown animals. Dosage compensation was first reported in Drosophila in 1932, and genetic compensation in response to a gene knockout was first reported in yeast in 1969. Since then, genetic compensation has been documented many times in a number of model organisms; however, our understanding of the underlying molecular mechanisms remains limited. In this review, we revisit studies reporting genetic compensation in higher eukaryotes and outline possible molecular mechanisms, which may include both transcriptional and posttranscriptional processes.

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Journal Article

Genetic compensation induced by deleterious mutations but not gene knockdowns

TL;DR: In this article, the authors show that egfl7 mutants do not show any obvious phenotypes while animals injected with egfl 7 morpholino (morphants) exhibit severe vascular defects, indicating that the activation of a compensatory network to buffer against deleterious mutations was not observed after translational or transcriptional knockdown.
Journal ArticleDOI

IGF-Binding Proteins: Why Do They Exist and Why Are There So Many?

TL;DR: The emerging explanation that many IGFBP functions have evolved to allow the targeted adjustment of IGF signaling under stressful or irregular conditions, which would likely not be revealed in a standard laboratory setting are explored.
Journal ArticleDOI

Highly Efficient CRISPR-Cas9-Based Methods for Generating Deletion Mutations and F0 Embryos that Lack Gene Function in Zebrafish

TL;DR: Supernumerary guanine nucleotides at the 5' ends of single guide RNAs (sgRNAs) account for diminished CRISPR-Cas9 activity in zebrafish embryos and heritable deletion mutations of at least 50 kbp can be readily induced using pairs of duplex guide RNPs targeted to a single chromosome.
References
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Journal ArticleDOI

Downregulation of the microtubule associated protein Tau impairs process outgrowth and myelin basic protein mRNA transport in oligodendrocytes

TL;DR: It is demonstrated that tau is important for MBP mRNA transport and involved in process formation, and the disturbance of the balance of tau leads to abnormalities in oligodendrocyte differentiation, neuron‐glia contact formation and the early myelination process.

Transcription oftheConstitutively Expressed YeastEnolase Gene ENOJIsMediated byPositive andNegative cis-Acting Regulatory Sequences

TL;DR: It is concluded that the negative regulatory element plays the critical role in maintaining the constitutive expression of the ENO1 structural gene in cells grown on glucose or gluconeogenic carbon sources.
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Drosophila abl and genetic redundancy in signal transduction

TL;DR: Molecular isolation and analysis of the genes identified by second-site mutations should define the molecular basis for the genetic redundancy in Drosophila Abl.
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Redundant functions of the genes knirps and knirps-related for the establishment of anterior Drosophila head structures

TL;DR: It is shown that the two biochemically equivalent gene products are both functional in the head anlage and that the lack of one gene activity can be overcome by the activity of the other, which provides a region-specific buffering system, rather than a case of global functional redundancy.
Journal ArticleDOI

Knockout of the prion protein (PrP)-like Sprn gene does not produce embryonic lethality in combination with PrPC-deficiency

TL;DR: It is established that double-knockout mice deficient in both Sho and PrPC are fertile and viable up to 690 d of age, and it is inferred that Sho’s activity will prove germane to the maintenance of neuronal viability in postnatal life.
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