ch 11 Flashcards

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1
Q

nuclear exosome

A

group of proteins that will break apart RNA that need to get got

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2
Q

cytoplasmic exosome

A

degraded after translation
after mRNA is done being translated and read this is done

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3
Q

rapid degration is done by

A

nonsense mediated mRNA decay

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4
Q

RNAi/ RNa interference

A

RNA is actively degraded, no translation

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5
Q

introns

A

removed from RNA, may have another function

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6
Q

exons

A

coding sequence for polypeptide, stuck together

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7
Q

primary RNA transcript

A

initial RNA before cutting

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8
Q

splice sites

A

where shit gets cuts, denotes the 5’ and 3’ sites
GU and AG

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9
Q

5 major splicing mechanism

A

1/2. autocatalytic group I and II introns
3. tRNA introns
4. arhcela introns
5. spliceosomal introns

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10
Q

splicosome

A

complex of riboprotiens that cut shit

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11
Q

where do the three mRNA maturing processes take place

A

c terminal of rna poly

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12
Q

what order does this shit occur in

A
  1. 5’ cap
  2. other shits
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13
Q

5’ cap contains

A

7 methylated guanosine

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14
Q

5’ cap function

A
  1. protect mRNA (from splicosome)
  2. facilitates loading onto small ribo subunit
  3. facilitate splicing
  4. 3’ end formation
  5. nuclear export
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15
Q

end sequence for poly tail to add

A

aauaaa, gu rich added by poly a polymerase (PAP)

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16
Q

aauaaa recognized by

A
  1. cleavage and polyadenylation specificity factor
  2. cleavage stimulation factor
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17
Q

RNa poly is terminated in part by

A

Xrn2 exonuclease
it chases RNA poly II and chews its ass

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18
Q

poly A tail is coated with

A

pabpn1 (binding protien), coated until it leaves

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19
Q

what gives rise to oculopharyneal muscular dystrophy

A

mutations is PABP1 (binding protein on poly a tail)

20
Q

largest and most complex molecular machine

A

spliceosome

21
Q

snRNAs and SM common core proteins invloed in splicing

A

5 snRNP (snurps)

22
Q

snRNA names

A

U1-6, no 3 tho

23
Q

5’ end sequence

A

GU

24
Q

3’ end sequence

A

AG

25
Q

ESE or ESS can- the splicing that will occur

A

silence or enhance

26
Q

alternative splicing

A

changing exon arrangement, variety (skipping and stuff)

27
Q

why is ok to only have small number of genes

A

alternate splicing- makes splice variants

28
Q

CaMKII delta has many isoroms due to

A

alt splicing, diff cellular locations

29
Q

cis splicing

A

exon on same gene get spliced together

30
Q

trans splicing

A

exon on different genes get splicing together (intra genetic, inter genetic, exo, endo)

31
Q

exo and endo spicing take dna form

A

plasmids

32
Q

RNA editing (post trans)

A

changing nucleotides after transcriptions

33
Q

RNA editing examples

A

adenine to inosine
cytidine to uridine

34
Q
A
35
Q

siRNA/ short interfering RNA

A

Silences same or similar locus from which they originate- from virus or eco genes

36
Q

miRNA

A

derived from unique genes that silence very diff genes

37
Q

dicer

A

processes dsRNA into shopt ds siRNA

38
Q

RISC

A

makes siRNA single stranded license thru RNA deflation or translation repression

39
Q

miRNA and siRNA difference

A

miRNA- encoded by organism
siRNA- external source

40
Q

what could silence dsRNA viruses

A

siRNA

41
Q

intron types

A

Autocatalytic Group I and Group II Introns,tRNA introns
* Archaeal introns
* Spliceosomal introns

42
Q

first transesterfication

A

The 2’-hydroxyl group of the branch point adenosine nucleotide attacks the 5’-splice site, forming a lariat structure

43
Q

second transesterfication

A

The 3’-hydroxyl group of the 5’-exon attacks the 3’-splice site, releasing the intron and joining the exons together.

44
Q

5’ cap added when

A

first

45
Q

CPSF

A

Cleavage behind the AAUAAA sequence is partly mediated b