Biological Molecules and Enzymes Flashcards

1
Q

sphingosine

A

like phosphoglycerides except that the glycerol is amino alcohol

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2
Q

Lipoprotein

Function and composition

A

fat carrier in the blood

hydrophobic core surrounded by phospholipids and apoproteins

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3
Q

T/F In absence of insulin, only brain and liver can absorb glucose

A

True

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4
Q

Starch

A

Glycogen for plants

Amylopectin and amylose

alpha linkage

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5
Q

Differentiate between nucleoside, nucleotide, and nucleic acid

A

Nucleoside - without phosphate (just nitrogenous base and sugar)

nucleotide - with the phosphate

nucleic acid - polymer with multiple nucleotides

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6
Q

AT, GC number of hydrogen bonds

A

AT: 2 hydrogen bonds

GC: 3 hydrogen bonds

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7
Q

Epigenetic

A

Changes made without changes in the nucleotie. ex. methylation

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8
Q

Nucleosome

A

8 histones wrapped around DNA

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9
Q

chromatin composition

A

1/3 DNA, 2/3 protein, little bit of RNA

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10
Q

Heterochromatin

A

tightly coiled and condensed, transcription doesn’t happen

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11
Q

Euchromatin

A

only coiled during nuclear division.

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12
Q

single-copy DNA

A
  • only one cop of a nucleotide sequence
  • regions of euchromatin that are actively transcribed
  • Long base sequences
  • Low rate of mutation
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13
Q

Repetitive DNA

A
  • Not translated - non coding regions of DNA
  • remain tightly coiled in heterochromatin
  • Short base sequences
  • Higher rate of mutation
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14
Q

Methylation

A

adding -CH3 on cytosine nucleotide. DNA wound more tightly so there is decrease in transcription

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15
Q

non-coding RNA

A

regions of RNA that doesn’t code for protein. Responsible for chemical changes in the chromatin structure

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16
Q

Promoter sequence function

A

Dictates where transcription takes place and how often transcription takes place

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17
Q

Is there a proofreading mechanism in transcription?

T/F: errors in RNA are called mutations

A

No

Errors in RNA are not called mutations and are not passed onto progeny

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18
Q

Termination in transcription

A

Termination sequence

Rho protein

19
Q

T/F activators and repressors only occur in prokarotes

20
Q

Lac Operon: explain the positive and negative control of how lac genes are transcribed

A

Positive control: Acceleration –> CAP activated by cAMP (secondary messenger); this activates the promoter sequence and allows the initiation complex to form

Negative control: lactose binding to the repressor and taking off the operator. Taking the break off.

The presence of lactose can induce the transcription of the lac operon only when glucose is not present

21
Q

5’ cap

A

attachment site during translation

protection from degradation of exonuclease

22
Q

snRNPs

A

snurps

ribozme that catalyzes chemical reaction on mRNA

snRNPS + associated proteins - spliceosome

23
Q

Alternative splicing

A

omitting exons, adding introns, utilizing various splicing sites

ending at different termination site, using a different promoter and etc - contribute to genetic diversity

24
Q

Introns function in gene expression

A

associated with amplified protein production

25
Destiny of proteins injected into the ER lumen
will become plasma membrane proteins of golgi, lslsome, ER, nuclear envelope, or secreted from the cell
26
Primse in DNA replication
creates RNA primer to initiate or jump start replication on the lagging strand
27
How are the primers removed in replication? How are the gaps filled?
RNAse H enzyme removes the primer. The gaps are filled by DNA polymerase
28
Stop codons
UAA, UGA, UAG
29
Signal for the large ribosome to join and form an initiation complex in translation
t-RNA carring 5'-CAU-3' sits on the P site
30
What happens when a stop codon reaches the A site?
protein known as the release factor attaches
31
Kinetochore
structure of protein and DNA located at the centromere of the joined chromatids of each chromosome
32
Transversion vs. transition
Both are base-pair substitutions Transversion: purine to pyrimidine or vice versa Transition: convert within purines or pyrimidines
33
Missense substitution
when a base pair changes a codon
34
Duplication in chromosomal mutation
When a segment of DNA breaks free and attaches onto a homologous chromosome
35
Translocation
Segment of DNA exchanged between chromosomes
36
Transposons
Flanked by flanking sequences, they can excise themselves out from the chromosome and reinsert themselves at another location
37
A way somatic cell can alter its genetic make up without meiosis
Transposition
38
Gene linkage
When genes on a chromosome are located close together. The are more likely to cross over together
39
Synaptonemal complex
Zipped region in chromosomes where genetic materials are being exchanged during meiosis
40
single cross over vs. double cross over
Single cross over: exchanging genetic information just once Double cross over: exchange a part of the chromosome then gets a sub section of it back (regains some of the original segment)
41
Penetrance
Probability of gene being expressed if it is present (binary condition, present or not)
42
Expressivity
how much the genotype is expressed as a phenotype degree of expression of a certain trait
43
Barr body
condensed, Inactive site on the X-chromosome. All but one X-chromosome is inactivated during interphase during gameoteogenesis. XX - one barr body XXX - two barr bodies
44
Hardy-Weinberg equilibrium Equation to predict allelic frequencies in a population
1) no selection for the fittest organism 2) random mating 3) large population 4) immigration or emigration must not change the gene pool 5) mutational equilibrium p^2 + 2pq + q^2 = 1 p + q = 1