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Tasya [4]
3 years ago
12

List as many reasons as possible why a cell will not survive without a nucleus

Biology
2 answers:
Dmitrij [34]3 years ago
9 0
A nucleus controls the movement of the cell, if that helps.
miss Akunina [59]3 years ago
5 0
All the RNAs needed for the cell are synthesised in the nucleus. The nucleolus within the nucleus is the site for RNA synthesis as well as DNA replication. ... A eukaryotic cell cannot survive without a nucleus and dies instantly. (There are exceptions like the erythrocytes which on maturity loses their nucleus).
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Using the sliding flament theory, explain (or draw) the process of sarcomere shortening. Start from the point where calcium woul
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  1. Calcium binds to troponin C
  2. Troponin T moves tropomyosin and unblocks the binding sites
  3. Myosin heads join to the actin forming cross-bridges
  4. ATP turns into ADP and inorganic phosphate and releases energy
  5. The energy is used to impulse myofilaments slide producing a power stroke
  6. ADP is released and a new ATP joins the myosin heads and breaks the bindings to the actin filament
  7. ATP splits into ADP and phosphate, and the energy produced is accumulated in the myosin heads, starting a new cycle
  8. Z-bands are pulled toward each other, shortening the sarcomere and the I-band, producing muscle fiber contraction.

Explanation:  

In rest, the tropomyosin inhibits the attraction strengths between myosin and actin filaments. Contraction initiates when an action potential depolarizes the inner portion of the muscle fiber. Calcium channels activate in the T tubules membrane, releasing <u>calcium into the sarcolemma.</u> At this point, tropomyosin is obstructing binding sites for myosin on the thin filament. When calcium binds to troponin C, troponin T alters the tropomyosin position by moving it and unblocking the binding sites. Myosin heads join to the uncovered actin-binding points forming cross-bridges, and while doing so, ATP turns into ADP and inorganic phosphate, which is released. Myofilaments slide impulsed by chemical energy collected in myosin heads, producing a power stroke. The power stroke initiates when the myosin cross-bridge binds to actin. As they slide, ADP molecules are released. A new ATP links to myosin heads and breaks the bindings to the actin filament.  Then ATP splits into ADP and phosphate, and the energy produced is accumulated in the myosin heads, which starts a new binding cycle to actin. Finally, Z-bands are pulled toward each other, shortening the sarcomere and the I-band, producing muscle fiber contraction.

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2 years ago
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