Biochemistry Molecular Flashcards

1
Q

What is the Chromatin structure?

A

DNA exists in the condensed, chromatin form
i n order to fit i nto the nucleus. Negatively
charged DNA loops twice around positively
charged h istone octamer to form nucleosome
“bead.” H istones are rich in the amino acids
lysine and argin i ne. Hl ties nucleosome beads
together in a string.
In mitosis, DNA condenses to form
chromosomes.

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2
Q

What is Heterochromatin?

A

Condensed, transcriptionally inactive, sterically
inaccessible.

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3
Q

What is Euchromatin?

A

Less condensed, transcriptionally active,
sterically accessible.

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4
Q

what is DNA methylation?

A

Template strand cytosine and adenine are
methylated i n DNA repl ication , wh ich allows
m ismatch repair enzymes to distinguish
between old and new strands in prokaryotes.

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5
Q

What is Histone methylation?

A

Inactivates transcription of DNA.

Methylation makes DNA Mute.

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6
Q

What is Histone acetylation?

A

Relaxes DNA coiling, allowing for transcription.

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7
Q

Which are the nucleotides?

Study Key

A
  • *PUR**i nes (A, G )-2 rings.adenine guanine
  • *PY**rimidines (C, T, U ) -1 ring. citosine,thymine,Uracil

Pure As Gold

CUT the PY

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8
Q

What is this?

A

Chromatin structure, Hl tying nucleosome beads

together in a string.

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9
Q

What are nucleotides?

A

Any of a group of molecules that, when linked together, form the building blocks of DNA or RNA: composed of a phosphate group, the bases adenine, cytosine, guanine, and thymine, and a pentose sugar, in RNA the thymine base being replaced by uracil.

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10
Q

Special caracteristics of Guanine, Thymine and Uracil?

A

Guanine has a ketone . Thymine has a methyl .
Deamination of cytosine makes uracil. Uracil found in RNA; thymine in DNA.

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11
Q

What nucleotides do we see in DNA?

A

A,G,C,T

Adenine,Guanine,Cystosine and Thymine.

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12
Q

What nucleotides do we see in RNA?

A

A,G,C,U

Adenine, Guanine,Cytosine, and Uracil

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13
Q

What is the difference in structure between Adenine and Guanine?

A

The process of deamination, the removal of the amino group

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14
Q

What is the enzyme that removes the amino group from adenine called?

A

adenosine deaminase

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15
Q

What does the deficiency of adenosine deaminase cause?

A

severe combined imunodeficiency (autosomal recesive)

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16
Q

What is the difference between Cytosine, Uracil and Thymine?

A

Guanine has a ketone . Thymine has a methyl .
Deamination of cytosine makes uracil.

17
Q

The methylation of uracil to thymine is catalyized by which enzyme?

A

Thymidylate synthase

18
Q

What can inhibit thymidylate synthase?

A

5 fluorouracil (5 FU)

19
Q

What is the difference between nucleosides and nucleotides?

A

A nucleoside is a nitrogen base + sugar

A nucleotide is a nitrogen base + sugar + phosphate

20
Q

What carbon in the sugar of the nucleotide helps diferentiate from DNA or RNA?

A

the 2 prime which either makes it deoxy if its absent or a ribose if its present

21
Q

What aminoacids are necessary for purine synthesis?

A

GAG

Glycine, Aspartate, and Glutamine.

22
Q

What does ribonucleotide reductase do?

A

Ribonucleotides are synthesized first and
are converted to deoxyribonucleotides by
ribonucleotide reductase

23
Q

What blocks de novo purine synthesis?

A

6-mercaptopurine (6-MP)

24
Q

What inhibits dihydrofolate reductase?

A

Methotrexate ( MTX)

25
Q

What inhibits bacterial dihydrofolate reductase

A

Trimethoprim (TMP)

26
Q

What is Orotic aciduria?

A
Inability to convert orotic acid to UMP (de novo pyrimidine synthesis pathway) because of defect in
 UMP synthase (a bifunctional enzyme).

Autosomal recessive.

27
Q

What can one expect to find in Ortic aciduria?

A

increase orotic acid in urine, megaloblastic anemia (does not improve with administration of vitamin B12
or folic acid), failure to thrive. No hyperammonemia (vs. OTC deficiency- increase orotic acid with
hyperammonemia).

28
Q

What is the treatment of Ortic aciduria?

A

Oral uridine administration.

29
Q

What happens in Adenosine deaminase deficiency?

A

Excess ATP and dATP imbalances nucleotide
pool via feedback inh ibition of ribonucleotide
reductase which prevents DNA synthesis and thus
decrease in lymphocyte count. One of the major causes
of SCID. Autosomal recessive.

1st di sease to be treated by experimental human
gene therapy.

30
Q

What is Lesch-Nyhan syndrome?

A

Defective purine salvage owing to absence of
HGPRT, which converts hypoxanthine to IMP
and guanine to GMP. Results in excess uric
acid production and de novo purine synthesis.
X-linked recessive.

31
Q

What are the clinical finding in Lesch-Nyhan syndrome?

A

retardation , self-mutilation,
aggression, hyperuricemia, gout,
choreoathetosis.

32
Q

What bond holds nucleotidesfrom the same strand together in DNA?

A

Phosodiester bond (PDE)

33
Q

What 2 properties does the dsDNA have?

A
  1. -Complementary (A-T) (G-C)
  2. -Antiparallel
34
Q

What bonds hold the dsDNA together?

A

3 hidrogen bonds(G-C)

2 hidrogen bonds (A-T)

35
Q

What does chargaffs rule say?

A

that the %A= %T(%U) and that the %G= %C only in dsDNA

36
Q

How many bases do we usually find in a turn of DNA?

A

10 bases per turn

37
Q

What is DNA denaturation?

A

The denaturation of nucleic acids such as DNA due to high temperatures is the separation of a double strand into two single strands, which occurs when the hydrogen bonds between the strands are broken. This may occur during polymerase chain reaction.

38
Q

What is DNA renaturation?

A

The reformation of double stranded DNA from thermally denatured DNA. The rate of reassociation depends upon the degree of repetition and is slowest for unique sequences

39
Q
A