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Related Concept Videos

Septins01:19

Septins

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Septins are protein filaments forming the cytoskeleton along with the microtubules, microfilaments, intermediate filaments, and other accessory proteins. In 1971 while studying the cell division cycle in mutant Saccharomyces cerevisiae Harwell et al. first identified the septin-related genes playing a crucial role in yeast cytokinesis. Fluorescence microscopy revealed that these proteins localize at the budding neck as rings. These ring-like proteins were then named Septins by John Pringle, and...
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Mutations01:39

Mutations

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Overview
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Mutations01:35

Mutations

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Mutations are changes in the sequence of DNA. These changes can occur spontaneously or they can be induced by exposure to environmental factors. Mutations can be characterized in a number of different ways: whether and how they alter the amino acid sequence of the protein, whether they occur over a small or large area of DNA, and whether they occur in somatic cells or germline cells.
Chromosomal Alterations Are Large-Scale Mutations
While point mutations are changes in a single nucleotide in...
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Role of Septins01:02

Role of Septins

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Septins are the recently discovered fourth major protein component of the cytoskeleton, along with microfilaments, microtubules, and intermediate filaments. These proteins can associate with other cytoskeletal filaments and carry out varied roles or can be free-floating in the cytoplasm.
Cellular Functions of Septins
Recent studies have revealed the multifaceted roles of septins in various cellular processes such as cytokinesis, ciliogenesis, and neurogenesis. Septins act as scaffolds and...
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Viral Mutations00:36

Viral Mutations

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A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material...
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Mutation, Gene Flow, and Genetic Drift01:09

Mutation, Gene Flow, and Genetic Drift

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In a population that is not at Hardy-Weinberg equilibrium, the frequency of alleles changes over time. Therefore, any deviations from the five conditions of Hardy-Weinberg equilibrium can alter the genetic variation of a given population. Conditions that change the genetic variability of a population include mutations, natural selection, non-random mating, gene flow, and genetic drift (small population size).
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Related Experiment Video

Updated: Feb 5, 2026

Reconstitution of Septin Assembly at Membranes to Study Biophysical Properties and Functions
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Reconstitution of Septin Assembly at Membranes to Study Biophysical Properties and Functions

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Septin mutations and phenotypes in S. cerevisiae.

Alexander Mela1, Michelle Momany1

  • 1Department of Plant Biology, University of Georgia, Athens, GA 30602.

Cytoskeleton (Hoboken, N.J.)
|September 2, 2018
PubMed
Summary

Septins are essential cytoskeletal proteins involved in cell division and polarity. This study maps known mutations in Saccharomyces cerevisiae septin genes onto protein structures, revealing functional consequences.

Keywords:
domainsmotifsphenotypesseptinsstructure

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Area of Science:

  • Cell Biology
  • Molecular Biology
  • Biochemistry

Background:

  • Septins are conserved GTP-binding proteins forming cytoskeletal structures in eukaryotes.
  • They are crucial for cellular processes like cytokinesis, cell polarity, and partitioning.
  • Saccharomyces cerevisiae is a well-established model organism for studying eukaryotic biology due to its genetic tractability and sequenced genome.

Purpose of the Study:

  • To provide a comprehensive overview of known point mutations in the seven Saccharomyces cerevisiae septin genes.
  • To map these mutations onto the three-dimensional structures of septin proteins.
  • To correlate mutation locations with conserved motifs and understand their functional impacts.

Main Methods:

  • Literature review and data compilation of known septin mutations in Saccharomyces cerevisiae.
  • Bioinformatic analysis and visualization of mutation sites on published septin protein structures.
  • Functional annotation of mutation effects based on existing literature and structural context.

Main Results:

  • Detailed mapping of point mutations across the seven S. cerevisiae septin genes (CDC3, CDC10, CDC11, CDC12, SHS1, SPR3, SPR28).
  • Identification of conserved motifs within septin proteins and their association with specific mutation sites.
  • Correlation of mutation locations within protein domains to observed functional consequences.

Conclusions:

  • Understanding septin mutations provides insights into their essential roles in cellular functions.
  • Structural mapping of mutations aids in deciphering the molecular mechanisms underlying septin function and dysfunction.
  • This synopsis serves as a valuable resource for researchers studying septin biology and cytoskeletal dynamics.