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Bursicon

Bursicon (from the Greek bursikos, pertaining to tanning) is an insect hormone which mediates tanning in the cuticle of adult flies.

Structure

The molecular structure of the hormone has been characterized rather recently. Bursicon is a 30 kDa neurohormone heterodimeric protein which is encoded by CG13419 gene and made of two cysteine knot subunits, Burs-α and Burs-β.

It is nondialyzable and loses its activity in alcohol, acetone, some proteases and trichloroacetate, renaturates after adding ammonium sulfate.

Function

Bursicon plays a very important role in insect wing expansion during the last step of metamorphosismaturation of the wing. At this time, the newly emerged adult removes dead cells of larval tissues. In Drosophila and Lucilia cuprina fly, the epidermis of wing is detached by extensive cell death apoptosis, at the time of wing spreading.

The cells that undergo death are removed from the wing cuticle and are absorbed into the thoracic cavity through wing veins. Subsequent wing maturation is disrupted if the process of cell death is inhibited or delayed somehow.

Bursicon is released just after eclosion and induces epidermis cell death. At the same time it hastens the tanning reaction, and hardens the newly expanded cuticle of the wing.

Where the peptide is found

Bursicon is found in different insects and considered to be unspecific. It is produced by median neurosecretory cells in the brain, circulates in blood and stored in corpora cardiaca.

The structure of the protein has been investigated well in fruit fly (Drosophila melanogaster), and in some insect species bursicon gene has been sequenced, including the mosquito (Anopheles gambiae), cricket (Gryllus bimaculatus), locust (Locusta migratoria), and mealworm (Tenebrio molitor).

The hormone is also present in the silkworm (Bombyx mori), blow fly (Calliphora erythrocephala), and cockroach (Periplaneta americana).

Effect of absence

Firstly, mutants of Drosophila melanogaster that lack bursicon gene can not spread their wings after eclosion. Secondly, the elongated abdomen shape of a newly eclosed fly remains for a much longer period of time. In addition, the abdomen of a fly is less melanized.

Using hybridization and immunocytochemistry it has been shown that bursicon is colocalized with Crustacean Cardioactive Peptide (CCAP). CCAP is responsible for activation of the ecdysis motor program. Mutant flies that had a defect in CCAP neurons also couldn’t express bursicon.

I asked Copilot a few questions and got this:

The name “bursicon” is derived from the Latin word “bursa,” which means “purse” or “sac.” This name was chosen because bursicon is involved in the process of cuticle tanning and hardening, which can be thought of as “closing” or “sealing” the new exoskeleton after an insect molts. The hormone essentially helps to “seal the deal” on the new cuticle, ensuring it hardens properly and provides the necessary protection and structure for the insect.

While humans don’t have wings or an exoskeleton, there are some parallels in the way our bodies handle structural integrity and repair. Here are a few human processes that share similarities with the functions of bursicon in insects:

Human Parallels:

Collagen Production: Collagen is a protein that provides structure and strength to various tissues, including skin, bones, and tendons. The process of collagen synthesis and cross-linking is somewhat analogous to the cuticle tanning and hardening in insects.

Wound Healing: The human body’s wound healing process involves several stages, including clot formation, tissue regeneration, and remodeling. This process ensures that the skin and other tissues regain their integrity and strength after injury, similar to how bursicon helps harden and stabilize the insect cuticle after molting.

Bone Remodeling: Osteoblasts and osteoclasts are cells involved in the continuous process of bone formation and resorption. This dynamic remodeling ensures that bones maintain their strength and adapt to stress, akin to how bursicon ensures the proper hardening of the insect exoskeleton.

Hormonal Regulation:

Growth Factors: Various growth factors, such as transforming growth factor-beta (TGF-β) and fibroblast growth factor (FGF), play crucial roles in tissue repair and regeneration. These factors help coordinate the complex processes of cell proliferation, differentiation, and extracellular matrix production.

While these human processes are not direct equivalents to bursicon’s role in insects, they highlight the importance of structural integrity and repair mechanisms in both humans and insects.

The term “bursa” has given rise to several related biological terms, primarily associated with structures and conditions involving these fluid-filled sacs. Here are some key terms:

Related Terms:

Bursa: A small fluid-filled sac that provides cushioning and reduces friction between tissues such as bones, tendons, and muscles.

Bursae: The plural form of bursa.

Bursitis: Inflammation of a bursa, often caused by repetitive motion or pressure, leading to pain and swelling.

Synovial Bursa: A type of bursa lined with synovial membrane, found near joints and providing lubrication to reduce friction.

Adventitious Bursa: A bursa that forms in response to unusual shearing stresses, often over bony prominences.

Subcutaneous Bursa: A bursa located between the skin and underlying tissues, often forming in areas subject to pressure.

Submuscular Bursa: A bursa located between muscles and bones or between neighboring muscles.

Examples of Specific Bursae:

Prepatellar Bursa: Located in front of the kneecap, often involved in “housemaid’s knee” bursitis.

Trochanteric Bursa: Found near the hip joint, commonly associated with hip bursitis.

Olecranon Bursa: Located at the elbow, involved in “student’s elbow” bursitis.

These terms highlight the various types and functions of bursae in the body, as well as the conditions that can affect them.

References

  1. Dewey EM, McNabb SL, Ewer J, et al. (July 2004). “Identification of the gene encoding bursicon, an insect neuropeptide responsible for cuticle sclerotization and wing spreading”Curr. Biol14 (13): 1208–13. doi:10.1016/j.cub.2004.06.051PMID 15242619.
  2. Fraenkel G, Hsiao C, Seligman M (January 1966). “Properties of bursicon: an insect protein hormone that controls cuticular tanning”. Science151 (3706): 91–3. doi:10.1126/science.151.3706.91PMID 5908970S2CID 39062433.
  3. Huang J, Zhang Y, Li M, et al. (February 2007). “RNA interference-mediated silencing of the bursicon gene induces defects in wing expansion of silkworm”FEBS Lett581 (4): 697–701. doi:10.1016/j.febslet.2007.01.034PMID 17270178S2CID 21816309.
  4. Luo CW, Dewey EM, Sudo S, Ewer J, Hsu SY, Honegger HW, Hsueh AJ (February 2005). “Bursicon, the insect cuticle-hardening hormone, is a heterodimeric cystine knot protein that activates G protein-coupled receptor LGR2”Proc. Natl. Acad. Sci. U.S.A102 (8): 2820–5. doi:10.1073/pnas.0409916102PMC 549504PMID 15703293.

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