Kidney, ureter bladder and urethra
A cold front does count as weather, if you're looking for more info on cold fronts and warm fronts visit the site below.
http://www.weatherquestions.com/What_are_fronts.htm
Answer:
Letter E - exons are cut from the strand and removed
Explanation:
Letter A and B are incorrect because the poly-A tail and guanine cap are added to the 3’ and 5’ end respectively. They aid in translation of the mRNA, while serving as protection. The poly-A tail is repeated adenine nucleotides, while the guanine cap is a modified guanine nucleotide.
Letter C is incorrect because alternative splicing is one mechanism for generating variation, and is thought to be one of the reasons for why humans have smaller genomes than other organisms and still maintain high complexity. Alternative splicing is incredibly important because it produces more than one transcript from a pre-mRNA.
Letter D is incorrect because introns are the non coding portions of the mRNA. They are excised to make a smaller mRNA transcript, and one that contains all the protein genes.
This letter E is the correct answer, because exons are the coding portions of the mRNA, and are not excised during RNA processing.
Hope that helped! If I made a mistake, please let me know.
Answer:
- Calcium binds to troponin C
- Troponin T moves tropomyosin and unblocks the binding sites
- Myosin heads join to the actin forming cross-bridges
- ATP turns into ADP and inorganic phosphate and releases energy
- The energy is used to impulse myofilaments slide producing a power stroke
- ADP is released and a new ATP joins the myosin heads and breaks the bindings to the actin filament
- ATP splits into ADP and phosphate, and the energy produced is accumulated in the myosin heads, starting a new cycle
- 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.
