<h2>Evolution of phylogenies </h2>
Explanation:
- The genome of the endosymbiont is all the more firmly identified with individuals from the gathering in which it initially developed, while the nuclear genome of the inundating living being has its own evolutionary trajectory.
- The accumulation of various inheritable attributes after some time which prompted the arrangement of another species
- Nuclear and organellar genes advanced at various rates, clouding developmental connections.
- Some mitochondrial genomes have been decreased definitely in size, losing a large number of the protein genes encoded in creature mtDNA just as a few or all mtDNA-encoded tRNA genes.
- At ∼6 kb in size, the mitochondrial genome of Plasmodium falciparum (human intestinal sickness parasite) and related apicomplexans is the littlest known, harboring just three protein genes, profoundly divided and improved little subunit (SSU) and enormous subunit (LSU) rRNA genes, and no tRNA genes.
- In stamped differentiate, inside land plants, mtDNA has extended generously in size (>200 kb) if not in coding limit, with the biggest known mitochondrial genome right now.
MRNA is read 5->3
Start codons can vary depending on the cell/organism type although more generally for mRNA it is always: AUG which is always Methionine
Stop codons for mRNA are:
<span>UAG ("amber") , UAA ("ochre"), <span>UGA ("opal")
</span></span>
<span>5'-uaucc.aug.gca.cuu.uaa.ac-3'
M-A-L
Methionine-Alanine-Leucine
</span>
Answer:
If I increase the temperature of the water I think it will go faster because the water comes to a boil.
Explanation:
A few various areas which differ from each other
- Prophase i has homologous chromosomes involved whereas Phrophase ii has individual chromosomes involved
- Phrophase i only occurs in diploid cells whereas ii occurs in haploid cells
These are the only important points I can differentiate them with. Hope it helps :)
Answer:
A. the heterozygote advantage
Explanation:
Heterozygote advantage is the condition where the heterozygous individual has higher relative fitness than both homozygous dominant and homozygous recessive individual. This means that the heterozygote individual has higher chances of surviving than both the homozygous counterparts. Sickle cell anemia is a recessive inherited disorder in which oxygen carrying hemoglobin has an abnormal structure. Hence, the resultant RBCs are not spherical but have crescent sickle shape. The oxygen carrying capacity of such RBCs is drastically reduced but they are unaffected by malarial parasite due to their abnormal structure.
- A person with both the recessive genes for sickle cell would not be able to survive due to insufficient oxygen transport in body.
- A person with both the dominant genes would be free of sickle cell anemia but in case of malaria would not be able to survive as the normal RBCs would be hijacked by the parasite.
- A hetrerozygote would survive both in malaria and sickle cell condition since he has enough normal RBCs for oxygen transport but also has sickle cell RBCs which are unaffected by malarial parasite.
