Answer:
option 3
Explanation:
In non-homologous end joining, the break ends are directly ligated together without the need for a homologous template unlike the homologous repair. this form of repair uses short homologous sequences of DNA termed microhomologies to direct repair and these microhomologies are seen as single-stranded overhangs found on the ends of double-strand breaks. When the overhangs are perfectly compatible, NHEJ ligates and repair the break. When these overhangs are not compatible, imprecise repair leading to deletion of nucleotides can also occur which is much more common .
Answer:
Explained below:
Explanation:
Density-dependent factors are biological factors adopted by the population as a resource. The things can be like shelter, food, or different poor resources. Density-dependent factors affect fitful variations in the population as its density fluctuations. If the population is small, these portions typically support improved rates of birth and lower will be the death rates, empowering the population to increase and when the population is big and thick, these factors display that the birth rate is decreased and death rate became higher.
Answer: Although both are X-linked recessive conditions, and therefore more likely in males, with the single X-chromosome. The recessive allele in colour blindness occurs at a higher frequency in the population and is a mild condition. Thus colour blindness does occur to a lesser extent in females because it needs the double recessive condition. DMD is a severe, disabling condition with a limited lifespan, and recessive allele frequency much lower, so the double recessive condition in females is very rare.
Explanation: DMD is an X-linked recessive, “nearly always in males” suggest that it also occurs due to a new mutation or some rare condition e.g. double recessive from an affected father and carrier mother, or inactivation of the normal gene in a heterozygote. It is also found that the defective allele is not completely recessive and that female carriers may exhibit mild to moderate effects.
colour blindness is polygenic, although the genes are all X-linked. It is more common in males than females. Females can carry two recessive alleles and so express the phenotype, but this is uncommon because the frequency of the recessive gene is low.
There are similarities in that both are X-linked recessives, therefore commonly expressed in males, who only have one X chromosome. The gene frequency of the colour blindness recessive is much higher than that of DMD, so the double recessive condition, which affects females, is more likely to be seen with colour blindness. In addition, DMD is a severe condition associated with disability and limited lifespan, which reduces the probability of mating between an affected male and carrier female
The property of carbon that allows it to make very large organic molecules would be the ability of carbon to form a maximum of 4 covalent bonds. Due to its 4 valence or outermost electrons.
