Does it say what is dominate and what is recessive or hetero or home it would make it 10x easier for me to help
Answer:
Cytochrome c is an enzyme found in bacteria, fungi, plants and animals. Here it is given that the human amino acid sequence for cytochrome c differs at 12 locations from the sequence in horses and pigeons. This information might be useful for inferring in preliminary stages that horses and pigeons are closely related to each other since they both show similar amount of difference from humans.
However, this hypothesis is being made with respect to the the comparison between "humans and horses" and "humans and pigeons". To further test this hypothesis pigeons and horses should be directly compared to each other without the use of a third species like humans. Hence, the sequence for cytochrome c in horse and pigeon should be compared with each other rather than comparing to humans.
D) A & B
it protects the seed against any damage or harmful weather conditions and also helps in dispersal of the seed through different means.
We examined the biogeographic patterns implied by early hominid phylogenies and compared them to the known dispersal patterns of Plio-Pleistocene African mammals. All recent published phylogenies require between four and seven hominid dispersal events between southern Africa, eastern Africa, and the Malawi Rift, a greater number of dispersals than has previously been supposed. Most hominid species dispersed at the same time and in the same direction as other African mammals. However, depending on the ages of critical hominid specimens, many phylogenies identify at least one hominid species that dispersed in the direction opposite that of contemporaneous mammals. This suggests that those hominids may have possessed adaptations that allowed them to depart from continental patterns of mammalian dispersal.
plz mark me as brainliest if this helped :)
Answer:
SNPs have shown that only 0.1 % of DNA sequences are different in the human genome between different individuals, thereby all the inherited phenotypic variation observed in our species is associated with only 0.1 % of differences at the genome level
Explanation:
Haplotypes are block-like sequences of DNA that are inherited together due to low recombination rates. Moreover, single-nucleotide polymorphism (SNP) mapping is a very useful methodology used to map the site of SNP mutations (i.e., SNP variants). In this regard, it has been observed that there are approximately 10 million common SNPs in the human genome. These SNPs contribute to the wide range of phenotypic variation observed in human populations for different traits (e.g., eye color, hair, weight, height, etc). Moreover, researchers have determined that SNPs can be clustered into haplotypes, thereby haplotypes can be accurately sampled by as few as approx. 300,000 selected SNPs, which are sufficient to represent all of the genetic variation across different human genomes.
