Preview

Essay On Sonic Hedgehog

Good Essays
Open Document
Open Document
1078 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Essay On Sonic Hedgehog
Sonic hedgehog (SHH) plays an important role in patterning various embryonic identities. (Johnson et al., 2014) Mutation in the sonic hedgehog enhancer leads to limb malformation in humans. There are 13 different point mutations and 10 duplications in humans involving the ZRS that have been shown to cause human malformation such as preaxial polydactyly, triphalangeal thumb and syndactyly. (VanderMeer and Ahituv, 2011) The role of the zone of polarizing activity control sequence (ZRS) is to produce and secrete SHH, which acts as a morphogen to control identity of each developing digit and specify the number of digits that form. (Gurnett et al., 2007) In this report I will discuss the type of mutation, identification of mutation, changes that …show more content…
This misexpression is central to a group of limb defects, which are known as ‘ZRS associated syndrome’. (Lettice et al., 2011) In humans, there are three classes of mutation that have been proposed based on the limb phenotypes; single based changes throughout the region causes preaxial polydactyly (PPD), single base changes at one specific site ,for example, a G>A transition at position 404, which causes Werner mesomelic syndrome (WMS), and large duplications that cause polysyndactyly. ‘‘Cuban mutation’’ is the cause of PPD type II, which is the result of mutation 404G>A of ZRS. (Wieczorek et al., …show more content…
This condition is usually inherited as autosomal dominant characteristic. There are two type of polydactyly; the pre-axial (extra digit towards the hand or foot) and post-axial (extra digit is towards the lateral margin of the hand or foot). Polydactyl can occur at the same time when excess digits are fused together, which is called polysndactyly. Patients with polydactyl can exhibit Werner mesomelic syndrome. This condition is characterised by a short limb dwarfism as a result of hypoplastic tibia. WMS occurs due to specific point mutation at position 404. (Cho et al., 2013) patients with WMS, can also exhibit duplication of the ZRS region, which is the cause of type Haas polysyndactyly or triphalangeal thumb polysyndactyly syndrome. This condition doesn’t affect lower limb development. This suggests that different mutational mechanisms affecting the enhancer region of the shh gene demonstrate different phenotypic outcomes. (Wieczorek et al.,

You May Also Find These Documents Helpful

  • Good Essays

    Then, in the early 1990s, new technology became available for scientists to discover what was really going on with ZPA and how it controlled the development of fingers and toes. At that point, Tabin, McMahon, and Ingham came up with the idea of comparing the chickens to flies. One gene, called hedgehog, made one end of a fly's body segment look different from the other, so the three laboratories began looking for a similar gene in chickens. They found one: Sonic…

    • 590 Words
    • 3 Pages
    Good Essays
  • Good Essays

    It is caused by a mutation in the DNA that codes for dystrophin. This is a protein that helps…

    • 451 Words
    • 2 Pages
    Good Essays
  • Powerful Essays

    Pt1420 Final Exam

    • 3892 Words
    • 16 Pages

    - caused by a MECP2 mutation. This gene is found on a person’s X chromosome…

    • 3892 Words
    • 16 Pages
    Powerful Essays
  • Good Essays

    Rupert Bunny Essay

    • 596 Words
    • 2 Pages

    Born in the 19th Century, Rupert Bunny was a renowned Australian artist. Endormies (pictured on the left) is an oil painting painted by this talented artist in 1904. This essay will outline Bunny’s style in painting, why he chose his subjects and what influenced him.…

    • 596 Words
    • 2 Pages
    Good Essays
  • Satisfactory Essays

    Townes-Brocks syndrome is an autosomal dominant inheritance syndrome that is caused by mutations in SALL1, which is located on 16q12.1 and whose gene product is a zinc finger protein that acts as a transcription factor gene (Kohlhase 2016). This syndrome is often caused by a variety of mutations such as nonsense, frame-shift, deletions, duplications and insertions. More severe cases have been related to a dominant negative or positive effect of a truncated protein (Stevens and May 2016). The prevalence is estimated to be about 1:250,000 (Kohlhase 2016). This syndrome can be caused by de novo pathogenic variants, which is the case about 50% of the time. If a parent has Townes-Brocks syndrome that is specifically caused by a pathogenic variant of SALL1, then their child has a 50% chance of also inheriting the syndrome (Kohlhase 2016).…

    • 365 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Alan Alexander Milne and Alexander McCall Smith are two of the world’s most beloved authors, and share much more than the name Alexander. These two authors wrote several children stories, and were quite famous. Although, their writing styles may differ, they share the ability for you to unhinge your mind and let it be free.…

    • 592 Words
    • 3 Pages
    Good Essays
  • Good Essays

    They frequently have mild to moderate short stature during childhood, but their growth usually catches up during puberty. Hand abnormalities are common in this syndrome and include short fingers (brachydactyly), curved pinky fingers (fifth finger clinodactyly), webbing of the skin between some fingers (syndactyly), and a single crease across the palm.…

    • 481 Words
    • 2 Pages
    Good Essays
  • Good Essays

    Manfar Sydrome

    • 477 Words
    • 2 Pages

    The gene defect also causes too much growth of the long bones of the body. This causes the tall height and long arms and legs seen in people with this syndrome. How this overgrowth happens is not well understood.…

    • 477 Words
    • 2 Pages
    Good Essays
  • Powerful Essays

    The gene that is responsible for causing Hurler Syndrome is on 4p16.3 site on chromosome 4 (Beesley, 2008). This gene is called iduronidase enzyme, otherwise known as IDUA (Beesley, 2008). IDUA is a type of gene that provides instructions on producing the enzyme alpha-L-iduronidase in order to break down glycosaminoglycans (GAGs) (Beesley, 2008). Generally, mutations reduce the production of this enzyme and increases GAGs within the lysosome cells (Beesley, 2008). Hurler Syndrome is an autosomal recessive disorder and is only expressed when an individual inherits two copies of the IDUA gene (Laberge, 2010). This disorder within the gene can be passed down to the next generation when a person has one mutated copy and a normal copy (Laberge, 2010). People that carry one IDUA gene produce less alpha-L-iduronidase enzyme than individuals with two genes (Laberge, 2010). However, this is enough to avoid Hurler Syndrome from developing (Laberge, 2010). It is estimated that about 0.7-1.6/100,000 people may be born with Hurler Syndrome (Laberge, 2010). Hurler Syndrome are most commonly caused by point mutations where only one change occurs with a sequence of nucleotides found within a gene (Keeling et al., 2001). Insertion and deletions of specific nucleotides affect the reading frame of codons within the gene (Keeling et al., 2001). The most commonly found mutation is a nonsense mutation where a single base pair or nucleotide is expressed at a premature stop codon (Keeling et al., 2001). The final result of the enzyme during translation does not fold and coil properly resulting in nonfunctional enzyme (Keeling et al., 2001). This all takes place from base pair 986,997 to base pairs 1,004,557 found on the short arm of the chromosome (Beesley, 2008). While the gene must contain 17 exons in order to function properly (Beesley,…

    • 1445 Words
    • 6 Pages
    Powerful Essays
  • Better Essays

    will occur if the mutation is on the maternally inheritetd chromosome 15. [See picture to the left] This accounts…

    • 924 Words
    • 4 Pages
    Better Essays
  • Good Essays

    Congenital malformation/anomalies can be defined as a physical defect that is present in a baby from birth. It can involve many different systems of the body including central nervous system, cardiovascular system, respiratory system, musculoskeletal system, gastrointestinal system, genitourinary system and reproductive system. These may include brain malformations, facial abnormalities, skin malformations, congenital heart diseases and bones malformations. These malformations are due to underlying genetic etiologies. The reported malformations included corpus callosum dysplasia for brain, cutaneous dyschromia for skin, ear malformations and brachydactyly for skeletal malformations. Caramaschi E, et al reported malformations and dysmorphism as predictors in which they defined malformation as major organ anomalies including the heart and genitourinary system29. However, they did not define the dysmorphisms.…

    • 536 Words
    • 3 Pages
    Good Essays
  • Powerful Essays

    Of Mice And Men Essay 2015

    • 2109 Words
    • 6 Pages

    3. Analyse the conventions and techniques the author uses to communicate the idea, using evidence from the novel. Where possible incorporate the quotes into the analysis.…

    • 2109 Words
    • 6 Pages
    Powerful Essays
  • Powerful Essays

    Ushers

    • 1750 Words
    • 7 Pages

    Of the eleven loci responsible for this syndrome, nine have already been identified. The proteins that are encoded by these genes are actually part of a dynamic protein complex that occurs in the hair cells of the inner…

    • 1750 Words
    • 7 Pages
    Powerful Essays
  • Good Essays

    Osteogenesis Imperfecta

    • 1054 Words
    • 5 Pages

    Osteogenesis Imperfecta was a severe, congenital genetic disorder which can cause the human bones to be extremely delicate. This disease is caused by a mutation(whether it be deletion or duplication) in chromosome 17q21, 31-q22, 7q22.1, which are the chromosomes that help the body produce the proteins to make collagen, which is what makes bones and muscles strong. Because of the body not being able to create collagen, the bones become very brittle and can increase the risk of fracture by a substantial amount. The lifespan of those with Osteogenesis Imperfecta differs due to how severe the disease is. The physical features of those with the OI are short stature, triangular shaped face, breathing problems, some hearing loss, brittle teeth, and bone deformities.…

    • 1054 Words
    • 5 Pages
    Good Essays
  • Better Essays

    Birth Defects

    • 2486 Words
    • 10 Pages

    genes out of 100,000 that make up who we are. This is caused by the genes…

    • 2486 Words
    • 10 Pages
    Better Essays

Related Topics