Paralogs

Paralogs are genes within the same organism that arose from duplication of an ancestral gene, making them distinct from orthologs, which diverge between species. Gene duplication can occur through unequal crossing over, replication errors, or whole-genome duplication; the resulting copies may retain the original function, divide it between them, or accumulate changes that produce new functions and expression patterns. Comparing paralog sequences, structures, regulatory regions, and expression profiles helps researchers reconstruct gene-family evolution, interpret genetic redundancy, and understand how complex biological pathways develop, while also informing studies of disease mechanisms and potential therapeutic targets.

Paralogs - Related Videos

Education

JoVE Core - Molecular Biology

Gene Families

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2020

Gene families consist of groups of genes proposed to have originated from a common ancestor. Typically these arise through events in which a gene or genes are mistakenly duplicated during cell division. Unlike their parent genes (which are subject to selection pressure to maintain function), these gene copies do not need to preserve their sequences and may evolve at a relatively faster rate. Occasionally these regions can be adapted to take on new roles within the organism, becoming novel genes...

Protein Families

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2020

Protein families are groups of homologous proteins; that is, they have similarities in amino acid sequences and three-dimensional structures. Protein families usually occur because of gene duplication, where an additional copy of a gene is inserted into the genome of an organism. Mutations that change the amino acids but still allow the protein to be properly synthesized, will lead to new protein family members. If these new proteins contain similar amino acids in key locations, protein...

Research

JoVE Journal - Biology

In Situ Immunofluorescent Staining of Autophagy in Muscle Stem Cells

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Cited by 2 •

2017

Active autophagy is associated with productive muscle regeneration, which is essential for Muscle Stem Cell (MuSC) activation. Here, we provide a protocol for the in situ detection of LC3, an autophagy marker in MyoD-positive MuSCs of muscle tissue sections from control and injured mice.

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