A major difference between mammalian spermatogenesis and oogenesis is <span>the number of gametes made per month.</span>
Answer:
The nucleus
Explanation:
Most DNA is located in the cell nucleus (where it is called nuclear DNA), but a small amount of DNA can also be found in the mitochondria (where it is called mitochondrial DNA or mtDNA). Mitochondria are structures within cells that convert the energy from food into a form that cells can use.
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Cuz they combine during fertilization and since 2 halves = 1 whole, u get gametes w a full number of chromosomes
Answer:
D. Aa
Explanation:
Given:
Jill (mother) is heterozygous for gene A --------- i.e Jill = Aa
Jack (father) who is homozygous recessive for gene A-------- i.e Jack = aa
Now if both cross and fertilization occurs, we have:
A a
a Aa aa
a Aa aa
The offsprings are (Aa, Aa, aa, aa)
Nondsijunction is the inability of homologous chromosomes to seperate properly during cell division. Now, we were told that this fertilization undergone nondisjunction in meiosis 1. Hence, both homologous chromosome move into the same daughter cells instead of different daughter cells because separation of homologous chromosome does not occur properly.
Therefore the result of these fertilization of a normal haploid sperm with an egg that had undergone nondisjunction in meiosis yields offspring with genotype Aa of their Mother (Jill).
Answer:
this mutation may change the open reading frame of the resulting RNA sequence and its final product, which is a protein in the case that this gene is used to synthesize a messenger RNA (mRNA) sequence
Explanation:
During the transcription, a region of DNA named 'gene' is used as template to produce an RNA molecule, typically a primary transcript of mRNA (pre-mRNA). Subsequently, this pre-mRNA suffers a process named RNA processing in order to generate a mature mRNA which is finally used to create a protein by a process called translation. If a deletion occurs during transcription, it may change the open reading frame (ORF) of the resulting mRNA when the mutation occurs in an exon of the protein-coding gene (i.e., occurs a frameshift mutation), while this deletion may not have any effect if it is localized within the introns which are removed during RNA processing. A frameshift mutation will change the amino acids that are added to the nascent polypeptide chain during translation.
