Documentation: Plasticity Data
These data are the results of a systematic curation of the literature on synaptic
plasticity in mice. We focused on papers studying the effects of mutations on
plasticity, particularly Long-Term Potentiation (LTP) and Long-Term Depression
(LTD).
Contents
Tissue
LTP decrease
LTP increase
LTD decrease
LTD increase
No effect
Other synaptic effects
Background
Synaptic plasticity is the ability of neurones to alter their responses to
each other, and is widely hypothesised to underpin learning. It is studied principally
by electrophysiology.
LTP refers to an enduring enhancement of synaptic transmission between two
or more neurones. It is typically elicited by high-frequency electrical stimulation.
Following this stimulation, the neurones respond more readily to each other;
this effect has been observed to last for a period of hours.
| Figure 1: Typical LTP
graph, obtained from the CA1 region of the
hippocampus |
LTD is the 'opposite' effect, an enduring reduction in synaptic transmission
between two or more neurones. It is produced by prolonged low-frequency stimulation.
We curated data from 259 papers studying the effects of mutations on synaptic
plasticity. We classified the plasticity effects into six categories, which
are described below. The brain region in which plasticity was studied was also noted and classified, as illustrated in the 'Tissue' field.
We also categorised the mutations into
six types; knockout, conditional knockout, point, truncation, over-expression
and other. These are represented in the data by abbreviations, to allow a more
precise description of the literature. For example, a gene may have been studied
using two different mutation types, both of which produce the same plasticity
effect. Our system makes such results apparent, without the need for the reader
to cross-reference.
In each plasticity effect column (LTP decrease, etc), one sees numbers followed
by a short letter string. The letters are the code used to represent the mutation
type. This is illustrated in the table below, which displays the codes used
to denote one of each mutation type.
| Mutation type |
Code |
| Knockout |
1ko |
| Over-Expression |
1ov |
| Point |
1po |
| Truncation |
1tr |
| Conditional |
1co |
| Other |
1ot |
So, for example, one might see that for one gene, in one particular brain
region, the 'LTP decrease' column reads '2ko, 1po'. This means that there are
two reports of knockout mutations producing an LTP decrease in that region,
and also one report of a point mutation producing an LTP decrease in that region.
Clicking on a data point opens up a new window which displays the paper referred
to and also provides more detailed information on the methods and protocols
employed.
Tissue
Name of the brain region in which synaptic plasticity was studied. Brain regions
were classified as belonging to one of the following categories:
| Hippocampal Regions |
Non-Hippocampal Regions |
| Generic Hippocampal |
Cerebellum |
| CA1-CA3 Schaffer Collateral / Commisural |
Striatum |
| Mossy Fibre |
Cortex |
| Dentate Gyrus |
Amygdala |
| Other |
|
LTP decrease
Number of reports, by mutation type, claiming that a mutation in this gene was
associated with an LTP decrease.
LTP increase
Number of reports, by mutation type, claiming that a mutation in this gene was
associated with an LTP increase.
LTD decrease
Number of reports, by mutation type, claiming that a mutation in this gene was
associated with an LTD decrease.
LTD increase
Number of reports, by mutation type, claiming that a mutation in this gene was
associated with an LTD increase.
No Effect
Number of reports, by mutation type, claiming that a mutation in this gene produced
no changes in synaptic plasticity.
Other synaptic effects
Number of reports, by mutation type, claiming that a mutation in this gene produced
a synaptic effect other than those delineated in the LTP and LTD columns. Examples
would include a change in baseline synaptic activity, reduced Paired-Pulse Facilitation,
etc.