hi all, could someone pls help me with this question
Gene regulation is the process of turning genes on or off in a particular cell.
a. State two advantages for an organism of being able to turn genes on or off in particular cells.
thank you
hi all, could someone pls help me with this question
Gene regulation is the process of turning genes on or off in a particular cell.
a. State two advantages for an organism of being able to turn genes on or off in particular cells.
thank you
One of them is because it's More efficient. Energy is not wasted by making proteins that are not needed.
I can't for the life of me remember the other.
Hey Guys, what is two primary types of genes?
yr12student22
I'm pretty sure the two primary types of genes we need to know about are structural and regulatory genes.
what are the biological consequence of increased genetic diversity? and what are the biological consequences of decreased genetic diversity?
yr12student22
Increased genetic diversity results in higher adaptive potential and lower chance of inbreeding. Conversely, decreased genetic diversity results in lower adaptive potential and a higher chance of inbreeding.
atarwonders
A second advantage could be prevents the overproduction of proteins which could accumulate in the cell
what happens to the resulting protein in silent mutation or nonsense?
Hi! In cellular Respiration, do we have to know the amount of inputs and outputs. For example, if theres 8 NAD, do we have to know the number because vcaa now expects us to know that only 26-28 atp is produced in aerobic respiration and even if we have to know the amount (of inputs and outputs) it is likely to be wrong in the books?? HELP PLS
AnanyaSharma as far as Iβm aware, itβs not necessary. In the past exams Iβve done itβs never been specified, you just need to know what the actual compounds are themselves.
Check the FAQ document they have a lot of stuff explained there. )
Love your pfp bahaha
AnanyaSharma you do need to know the ATP numbers (you'll see this in practice exams), but I don't think it's necessary for the other compounds like NADH and FADH2 (although, it can be helpful to understand the processes of aerobic cellular respiration. Also, just to note, the new ATP numbers are 30 or 32 ATP for aerobic cellular respiration (2 for glycolysis, 2 for the Krebs cycle, and 26 or 28 for the electron transport chain). You also need to say "or" instead of "-" from what I've heard.
God Yeah one of them is to save energy and resources and prevent production of a gene product when its not needed
And the second is to produce sufficient quantities of a specific gene product ex- ATP synthase in muscle cells that undergo high rates off aerobic cellular respiration due to their large ATP requirement
yr12student22 In a silent mutation theres no change to the proteinβs 3D tertiary structure as the single base substitution still codes for the same amino acid due to the degeneracy of the genetic code.
With missense although thereβs a change of one amino acid- it does not entirely change the 3D tertiary protein structure due to misfolding as a result of different interactions between the variable R groups of amino acids in the polypeptide chain. This wont be as significant of an effect compared to framshifts where the protein becomes non functional
Hey guys, i am really struggling with natural selection and selective breeding. can someone please give me a example that summaries it.
the main difference is what is acting as the selection pressure.
For natural selection, take the example of grey and black moths in an environment, the selection pressure is the predators who may see the grey moths better when they are against darker bark on trees. This will allow for the moths to be 'fitter' since they are selected by their environment.
for artificial selection think of cows being bred to produce more meat. Humans are the selection pressure selecting more meaty cows to breed together. In the end, they aren't necessarily 'fitter'.
hi! how do i answer this question;
Smallpox was one of the deadliest human viral diseases. People who survived this disease were often badly
scarred, blinded or both. In April 1789, 15 months after the British arrival to Australia, a major smallpox
outbreak occurred. In terms of the number of infected individuals and subsequent deaths, the outbreak
affected the Indigenous population to a greater extent than the British population.
a. The British population and the Indigenous population were both exposed to the smallpox virus.
Suggest one reason why the Indigenous population was affected to a greater extent than the British
population. Explain your response.
in my answer i stated the role of the antigen presenting cells was that the only thing needed? or do i have to implement 'smallpox virus' in my answer to get the full 3 marks
Do mutations or genetic drift have a greater effect on the gene pool?
Thanks
chemistry1111 Genetic drift since it tends to have a more profound and drastic effect on the gene pool, since the bottleneck effect wipes out much of a population and the founders effect can drastically reduce the gene pool its allele frequency due to migrating populations not genetically reflecting the many alleles found in the initial population (both populations, initial and founded, are usually greatly impacted). The effect of genetic drift can be even more pronounced in small populations, causing some to become extinct. Mutations occur all the time and are often quite small or random. Since they tend to only occur in one individual, they don't suddenly change the entire gene pool. Obviously, natural selection will alter the allele frequencies in response to a mutation and its possible advantages or disadvantages will alter the gene pool. However, you'd need a lot of mutations to have a sudden and drastic impact, and changes tend to occur gradually over time. Genetic drift is usually more sudden in its impact. The level of impact of mutations simply isn't the same as genetic drift tends to be. That said, I might be wrong, but that's sort of what I've been taught.
what's the relationship between the pathogen and antigen?
yr12student22 The antigen is a "body part" of the pathogen that your immune system recognises as foreign. Antigens can be proteins expressed by the pathogen, although there can be self-antigens produced by the body of someone affected by an autoimmune disease
what is the structure of monoclonal antibodies?
what's the relationship between innate and inflammatory response?
do naive t cells or cytotoxic t cells undergo clonal expansion?
atarwonders they consist of one big polypeptide (heavy chain) and one small polypeptide (light chain). They also have specific variable regions, which are complementary to the antigen. (the same as a normal antibody)
atarwonders you only need to talk about whether the Indigenous populations were able to develop immunity as well as the British (hint: British developed immunity at a younger age and thus already had antibodies, and Indigenous Australians were exposed to it for the first time)
atarwonders Hi there! For this question the main point is about prior immunity so for 3 marks Iβd say :β
chemistry1111 Naive T cells undergo clonal expansion and selection to form cytotoxic T cells or memory T cells
What is the underlying difference between a rule based approach and consequences based approach?
Example would really be nice
spicynuggets
Consequences-based approach = Aims to maximise the positive outcomes while minimising the negative outcomes.
Duty/rule-based approach = Promotes the responsibility of the agent above all else, and places importance on the duty of each individual.
Is rational drug design in the new study design?
Could someone please explain the function of the PAM sequence?
biology nope. That was from the last study design, so you can ignore these questions!
biology ok. So, the PAM sequence is a sequence of nucleotides called the protospacer adjacent motif (usually NNG, with N being any nucleotide). Viral DNA has many PAM sequences. When the protospacer is cut out of the viral DNA that has been injected into the bacteria, this is done a little after the PAM site by Cas1 and Cas2 (just other restriction endonucleases). The purpose of the PAM site is for the Cas9 cutting part of the CRISPR-Cas9 process. When the Cas9 enzymes identifies viral DNA and a PAM region on it, it opens up the DNA and sees whether or not the gRNA is complementary to the sequence of bases upstream from the PAM sequence but on the opposite strand. If the gRNA is complementary to the viral DNA section after the PAM sequence, it will cut the DNA on both strands just upstream from the PAM. However, if the gRNA does not match the viral sequence, Cas9 closes the viral DNA and continues to search for another PAM site (it can take multiple goes to find the right one since there are lots of PAM sites). So in summary, the PAM site is like a recognition tool or tag for Cas9 to search for and identify, allowing it to check the viral DNA with the gRNA before making a cut. Hope that makes sense!
what is the difference between social implication and biological implication? and also do we need to include that in sympatric speciation gene flow doesnt occur
_sophiestudies_ Thankyou so much!
for photosynthesis do you say the light dependent stage is the grana or thylakoid?
what is the role of rubisco?
clazah a granum is a stack of thylakoids, so u can say either i think
does anyone have access education biology exam
Is it okay to write exam in pencil