Chromatin Structure Part 3 Flashcards

1
Q

chromosome looping

A
  • how chromatin divided into functional domains within the nucleus
  • forms loops and condenses a lot
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2
Q

insulators

A
  • Boundaries between domain of the gene and the enhancer (or silencer)
  • the gene can no longer feel the activating (or repressing) effects
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3
Q

domain boundaries

A
  • special nucleoprotein structures formed by proteins at specific sites along the chromosome
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4
Q

how is inappropriate activation avoided?

A
  • organisms use DNA insulators to block activation of unrelated genes by nearby enhancers
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5
Q

insulator proteins

A
  • recruit histone acetyltransferases that acetylate flanking nucleosomes
  • inhibits histone modifications required for the propagation of transcriptionally silent condensed chromatin
  • prevents spread of heterochromatic DNA
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6
Q

boundary elements

A
  • relate structural organization of chromatin fiber into informational organization of the DNA
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7
Q

position effects

A
  • when genes relocated to new chromosomal environments by rearrangement or transformation
  • modifies gene expression
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8
Q

in vivo assay for boundary function

A
  • determine if DNA sequences can protect a reporter gene from chromosomal position effects
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9
Q

the site of insertion

A
  • helps determine the level of expression of the transgene
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10
Q

chromatin looping between elements facilitates transcription at submegabase level

A
  • initiation of transcription involves physical interaction between gene regulatory elements such as promoters and enhancers
  • may be separated by many kilo bases along the linear chromosome
  • DNA loops out so enhancer can interact with promoter to initiate transcription
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11
Q

topically associated domains (TADs)

A
  • chromosomes are further segregated into these containing many chromatin loops
  • separated by architectural proteins at their borders
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12
Q

architectural proteins (APs)

A
  • bend DNA and allow formation of loops

- also function as insulators

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13
Q

chromosome territories (CTs)

A
  • TADs further organized at entire chromosome level, forming these
  • non randomly organized in the nucleus and occupy distinct regions
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14
Q

lamin-associated domains (LADs)

A
  • nucleus further segmented into different compartments
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15
Q

repression facilitated by

A
  • associated of genomic sequences with the inner nuclear lamina through lamin binding proteins
  • gene position toward periphery of nucleus generally results in transcriptional repression
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16
Q

transcriptional neighborhoods (TNs)

A
  • contain a collection of transcriptional machinery
  • provide an environment for initiation and hyper activation and maintenance of transcription
  • multiple genes and regulatory elements founds within TNs
17
Q

directed chromatin movement

A
  • local compaction of chromatin by architectural proteins

- looping out of specific genomic regions

18
Q

local compaction of chromatin by architectural proteins

A
  • permits interaction between specific promoters and enhancers
  • bend DNA into topological domains
  • enables transcription of specific genes
19
Q

looping out of specific genomic regions

A
  • to form long-range interactions with distal enhancers requires some chromatin slack
  • decompact neighboring region
  • previously interacting enhancer/promoter loops sacrificed to permit new loops
  • allows interaction with promoters on different chromosomes
20
Q

domains are dynamic

A
  • change under development time or physiological conditions to allow for change in gene expression