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5-GCATGAGTCTGGTACGCTTTTAAAGC-3 3-CATGCG-5 IIIII 3. (a) in the sequence above, what enzyme would you need to extend the sho
After using a chemical mutagen to generate mutations in a DNA sequence, scientists noted a mutation from C to T at the 10th p
Lou Gehrig disease (aka ALS, amyotrophic lateral sclerosis) is a condition of progressive weakness and wasting of skeletal mu
Complete the drawing of a trinucleotide, number carbon atoms within the sugar components, indicate the nitrogenous bases and
We are looking at a schematic of a replication fork. (a) Which strand (B or D) is showing leading strand synthesis? (b) Name

genetic biology
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Answer #1

3. a) Primase enzyme makes an RNA primer, or short stretch of nucleic acid complementary to template, that provides 3' end for DNA polymerase to work on.

b) 3'CGTACTCAGACCATGCGAAAATTTCG5'

c) Phosphodiester bond

Mutations- Transversion

Transition

Induced point mutations

a) At the elongation stage expansion occurs.It includes repeat expansion within exon 1 of gene.

b) probability is 50 percent. because Prisha is a carrier.

Someone with autosomal dominant FALS has one copy of the gene with a mutation and one copy of the gene without a mutation. A child born to someone with FALS has a 50% chance of inheriting the FALS gene mutation and a 50% chance of inheriting the gene without the mutation.

Attaching image of trinucleotide DNA

DMTOO Base RO-P=0 07 Base RO-P=0 0-0 Basez R= c N ON CH3 H3C^CH3NH3 | 0 0— P=0 го—p=0 N NH2 о с нь дун o-p=0 тг Осн, сухо 0 ОН The DNA trinucleotide C-G-T

one of the major structural differences between DNA and RNA is sugar with the 2-deoxyribose in the DNA being replaced by ribose in RNA.

a) according to image B is a leading strand synthesize continuosly and  D is a lagging strand.

b) multiple proteins are required, DNA polymerase, SS DNA binding protein, Helicases, primase, topoisomerases and DNA gyrases.

c) telomerase adds complementary RNA bases to 3'end of DNA strand. so according to the image A will need to have telomerase activity.They function to protect the end of chromosomes from sticking to each other. They also protect genetic information during cell division because a short piece of each chromosome is lost every time its DNA is replicated.

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