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Title: Studying Segmentation Mutants in Balanced Stocks


1
Studying Segmentation Mutants in Balanced Stocks
2
Drosophila Development
  • Each egg is surrounded by a chorion.
  • The anterior end has two filaments to allow
    oxygen to enter the cell.
  • Sperm enter through the micropyle at the anterior
    end.

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Early Drosophila Development
  • It takes 1 day for the embryo to develop into a
    larva.
  • The larva hatches, feeds, and sheds its skin
    twice.
  • After 5 days, the larva becomes immobile and
    forms a pupa.
  • During the pupal stage, cells in the imaginal
    discs differentiate into adult structures.

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Maternal Gene Activity in Development
  • Materials transported into the egg during
    oogenesis play a major role in embryonic
    development.

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Maternal-Effect Genes
  • Maternal-effect genes contribute to the formation
    of healthy eggs effects of mutations in these
    genes may not affect the phenotype of the female
    making the eggs but may be seen in the next
    generation.
  • A maternal-effect mutation causes a mutant
    phenotype in the offspring of a female with a
    mutant genotype.

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The dorsal GeneOffspring of dl/dl Females are
Dorsalized and Inviable
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Segmentation Genes
  • Segmentation genes are required for segmentation
    along the anterior-posterior axis.
  • They are classified into three groups based on
    embryonic mutant phenotypes.
  • Gap genes
  • Pair-rule genes
  • Segment-polarity genes

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Gap Genes
  • Gap genes define segmental regions in the embryo.
  • Mutations in the gap genes cause a set of
    contiguous body segments to be missing.
  • Four gap genes have been well characterized
    Krüppel, giant, hunchback, and knirps.
  • Gap gene expression is controlled by bicoid and
    nanos.
  • The gap genes encode transcription factors.

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Pair-Rule Genes
  • Pair-rule genes define a pattern of segments
    within the embryo.
  • Pair-rule genes are regulated by the gap genes
    and are expressed in seven alternating bands,
    dividing the embryo into 14 parasegments along
    the anterior-posterior axis.
  • In pair-rule mutants, every other parasegment is
    missing.
  • The pair-rule genes encode transcription factors.

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Expression of fushi tarazu (ftz) in a Drosophila
Blastoderm Embryo
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Segment-Polarity Genes
  • Segment-polarity genes define the anterior and
    posterior compartments of individual segments.
  • Mutations in segment-polarity genes cause part of
    each segment to be replaced by a mirror-image
    copy of an adjoining half-segment.
  • Segment-polarity genes refine the segmental
    pattern established by the pair-rule genes.
  • These genes encode transcription factors and
    signaling molecules.

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Segmentation Gene Mutants
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Chapter 21The Genetic Control of Animal
Development
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Sex Determination in Drosophila and C. elegans
  • The sex determination signal in both animals is
    the ratio of X chromosomes to autosomes. If the
    ratio is 1.0 or greater, the animal is a female
    if the ratio is 0.5 or less, the animal is a
    male.CLASSIC Definition
  • But wrong
  • In Drosophila, the key genes in sex determination
    encode proteins that regulate RNA processing.

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Sex Determination in Drosophila
  • Components of the sex-determination pathway
    include
  • A system to ascertain the XA ratio ,
  • A system to covert this ratio into a
    developmental signal, and
  • A system to respond to this signal by producing
    either male or female structures.

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Ascertaining the XA Ratio
  • The system that ascertains the XA ratio involves
    interactions between maternally synthesized
    proteins in the egg cytoplasm and embryonically
    synthesized proteins encoded by several X-linked
    genes.
  • The X-linked gene products are called numerator
    elements and are twice as abundant in XX embryos
    as in XY embryos.
  • The autosomal gene products are called
    denominator elements and antagonize the products
    of the numerator elements.

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The Sex-lethal (Sxl) Gene
  • Sxl is the mater regular of the sex
    determination pathway in Drosophila.
  • The XA ratio is converted into a molecular
    signal that controls the expression of the
    X-linked Sxl gene.

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Function of SXL
  • SXL regulates splicing of its own transcript to
    maintain SXL protein expression in XX embryos.
  • SXL also regulates splicing of the transformer
    (tra) gene.

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Differentiating in Response to the Signal
  • TRA, along with TRA2, regulate splicing of
    doublesex (dsx) and fruitless (fru).
  • In XX embryos, where TRA is present, dsx
    transcripts are processed to encode a DSX protein
    that represses the genes for male development.
  • In XY embryos, where TRA is absent, dsx
    transcripts are processed to encode a DSX protein
    that represses the genes for female development.

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Fruitless (fru)
  • Males homozygous for the fru mutation court other
    males.
  • The fru gene encodes a zinc-finger transcription
    factor that regulates the genes for male sexual
    behavior.

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Loss-of-Function Mutations in Sex-Determination
Genes in Drosophila
  • Mutations in Sxl prevent SXL protein from being
    made in males homozygous mutants would develop
    into males but die as embryos.
  • Mutations in transformer and transformer2 cause
    both XX and XY animals to develop into males.
  • Mutations in dsx cause both XX and XY embryos to
    develop into intersexes.

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Key Points
  • In Drosophila the pathway that controls sexual
    differentiation involves some genes that
    ascertain the XA ratio, some that convert this
    ratio into a developmental signal, and others
    that respond to the signal by producing either
    male or female structures.
  • The Sex-lethal (Sxl) gene plays a key role in
    Drosophila sexual development by regulating the
    splicing of its own transcript and that of
    another gene (tra).

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