molec cell final 2025

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571 Terms

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transcription

first step in gene expression

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RNA polymerase

enzyme that catalyzes the synthesis of RNA from a DNA template

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number of subunits in bacterial RNA polymerase

five

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function of the σ subunit in bacterial RNA polymerase

identifies the correct sites for transcription initiation and binds first

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promoter

gene sequence upstream of transcription start site to which RNA polymerase initially binds

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promoter length in prokaryotes

6 nucleotides

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prokaryote promoter locations

10 and 35 base pairs upstream of the transcription start site

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bacterial RNA polymerase unwinds this many bases of DNA for transcription

12 - 14

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the σ subunit is released after:

addition of ~10 nucleotides

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function of the ß and ß’ subunits in bacterial RNA polymerase

form a claw-like structure that grips the DNA template

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stop signal

terminates transcription in prokaryotic RNA synthesis

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most common stop signal in E. coli

repeat of a GC-rich sequence followed by 7 A residues

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result of transcribing the GC-rich repeat in E. coli

RNA forms a stable stem-loop structure

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chromatin

location of transcription in eukaryotes

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number of RNA polymerase in eukaryotes

3

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RNA polymerase II

synthesizes mRNA

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RNA polymerase III

synthesizes tRNA and rRNA 5S

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RNA polymerase I

synthesizes rRNA 5.8S, rRNA 18S, and rRNA 28S

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general transcription factors

proteins involved in transcription from polymerase II promoters

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TATA box

promoter for RNA polymerase II that resembles the -10 sequence of bacterial promoters

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5 general transcription factors that form the preinitiation complex

TFIID, TFIIB, TFIIF, TFIIE, TFIIH

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TFIID

general transcription factor that initially binds the TATA box (or other promotor region)

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mediator

protein complex of more than 20 subunits that interacts with both the general transcription factors and RNA polymerase II

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process that starts gene transcription

phosphorylation of the polymerase CTD by the TFIIH protein kinase

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process that stops gene transcription

RNA polymerase II reaches the terminal signal

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process that follows transcription of the terminal signal

RNA endonuclease cleaves RNA polymerase II from the DNA

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number of transcription factors that recruit RNA polymerase I

2

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general ribosome structure

1 small subunit + 1 large subunit

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<p>size of the mammalian ribosome</p>

size of the mammalian ribosome

80S

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<p>size of the large subunit in a mammalian ribosome</p>

size of the large subunit in a mammalian ribosome

60S

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<p>size of the small subunit in a mammalian ribosome</p>

size of the small subunit in a mammalian ribosome

40S

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<p>components of the large subunit</p>

components of the large subunit

28S rRNA + 5.8S rRNA + 5S rRNA + 49 proteins

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<p>components of the small subunit</p>

components of the small subunit

18S rRNA + 33 proteins

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number of promoter types for polymerase III

3

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1st step of pre-rRNA modification

cleavage of rRNA

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2nd step of pre-rRNA modification

ribose methylation

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3rd step of pre-rRNA modification

uridine isomerization to pseudouridine

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snoRNA function

guides modification of pre-rRNA

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snoRNP

RNA/protein complex formed with snoRNA to carry out modification

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processing of the 5’ end of pre-tRNA

cleavage by the ribozyme RNase P

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processing of the 3’ end of tRNA

addition of a CCA terminus

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modified bases formed by modification of uridines in tRNA

dihydrouridine and ribothymidine

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modified bases formed by modification of guanosines in tRNA

inosine and methylguanosine

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when are pre-mRNAs extensively modified

before export from the nucleus

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addition of a 7-methylguanosine cap

modification of the 5’ end on mRNA

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polyadenylation (addition of a poly-A tail)

modification of the 3’ end on mRNA

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G-U rich downstream sequence

signal for polyadenylation

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hexanucleotide (AAUAAA)

signal for polyadenylation

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number of adenines added by poly-A polymerase to form the poly-A tail

200

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1st step of pre-mRNA splicing

cleavage at the 5’ splice site, loop forms by joining the 5’ end of the intron to an A within the intron (branch point)

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2nd step of pre-mRNA splicing

cleavage at the 3’ splice site, simultaneous excision of the exons from the loop

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spliceosomes

five types of snRNAs

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5 types of spliceosomes

U1, U2, U4, U5, U6

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snRNP structure

6 - 10 protein molecules complexed with a snRNA

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this snRNA binds to the 5’ splice site of pre-mRNA by base pairing recognition

U1

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this snRNA binds to the branch point of pre-mRNA

U2

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these snRNAs act together to form the intron loop of pre-mRNA

U4, U5, U6

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fate of apolipoprotein B when translated from unedited mRNA

synthesized in the liver

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fate of apolipoprotein B when translated from edited mRNA

synthesized in the intestine

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turnover rate of rRNA

stable (lasts a long time)

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turnover rate of tRNA

stable (lasts a long time)

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turnover rate of mRNA

very quick; degrades rapidly

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short-lived mRNAs code for

regulatory proteins

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mRNAs with long half-lives code for

structural proteins

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shortening of the poly-A tail

initiates mRNA degradation

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regulation of mRNA degradation

extracellular signals, siRNA, miRNA

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introns

noncoding sequences

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introns are removed at this step of mRNA

splicing

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basal laminae

thin layers on which epithelial cells rest, surrounds muscle cells, adipose cells, peripheral nerves

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major structural protein

collagen

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collagen structure

triple helix consisting of a repeating glycine-X-Y sequence

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typical amino acid in the X position for collagen

proline

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typical amino acid in the Y position for collagen

hydroxyproline

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hydroxyl groups

stabilize the triple helix in collagen by forming hydrogen bonds

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most abundant form of collagen

Type 1 collagen

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type 1 collagen function

forms collagen fibrils in which the triple helical molecules form regular staggered arrays

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covalent cross-links

bonds between side chain residues that help strengthen the fibrils

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importance of collagen covalent cross-links in medical science

forms and repairs tissues

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type of collagen in brain tissue

type IV collagen

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glycosaminoglycans (GAGs)

polysaccharides formed from repeating units of disaccharides; form extracellular matrix gels

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fundamental unit of GAGs (except for hyaluronan)

dimers

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GAG found in cartilage, brain tissue, and neural tissue

hyaluronan

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GAGs found in dermis tissue

dermatan sulfate, keratan sulfate

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GAGs found in many different tissues

chondroitin sulfate, heparan sulfate

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charge on GAGs due to sulfate groups

highly negative charge

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only GAG that is a single long polysaccharide chain

hyaluronan

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proteoglycans

formed by GAGs linked to proteins

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function of hyaluronan

interacts with proteoglycans to form large complexes in the extracellular matrix

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main adhesion protein of connective tissues

fibronectin

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molecules for which fibronectin has binding sites

collagen, GAGs, and integrin

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adhesion proteins in basal laminae

laminins

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laminin structure

3 polypeptide chains, each with rod-like domains interspersed with globular domains, and binding sites on the subunits

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structure formed by multiple laminins

networks

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adhesion protein that is tightly associated with laminins

nidogen

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type of collagen that nidogen binds

type IV collagen

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structure of integrin

dimer formed by an α subunit and a ß subunit

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number of possible α subunits in integrin

18

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number of possible ß subunits in integrin

8

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number of different integrins

24

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extracellular matrix molecules bound by integrin

collagen, fibronectin, laminin, cytoskeleton