Playing catch-up
research highlights
Proteomic analysis
Neurophysiology
Nat. Commun., https://doi.org/10.1038/s41467018-04957-4 (2018)
Elife, https://doi.org/10.7554/eLife.34275 (2018).
Protein modification
analysis in depth
In eukaryotes, small ubiquitin-like modifier
(SUMO) is a protein family with four
different isoforms (S1 to S4) that has
enzymes dedicated to conjugating SUMO
to target proteins. SUMOylation impacts
enzyme location and function and has been
implicated in cell division, nuclear transport,
and transcriptional regulation. In a new
report, investigators describe a method
to isolate S2 and S3 conjugated peptides,
which does not rely on engineered cell
lines or animals carrying a tagged variant
of SUMO to facilitate enrichment. The
authors identified more than 14,000 sites in
human cell culture and nearly 2000 across
eight different mouse tissues. In cell culture,
a much larger fraction of SUMO2/3 pools
were conjugated to targets and is consistent
with other reports of high SUMOylation
levels in rapidly dividing tissues. Brain
had the fewest sites of any mouse tissue
and is surprising given that SUMO has
been implicated in some neuropathologies.
This dataset will serve as a reference of
SUMOylation in normal/healthy tissues. CN
https://doi.org/10.1038/s41684-018-0123-7
Mapping behaviors to
descending neurons
In vertebrates and invertebrates,
environmental information is processed
in the brain and behavioral signals passed
through descending neurons to regulatory
centers that are proximal to effectors
i.e. muscles. For Drosophila, only ~1100
neurons relay information to the ventral
nerve cord that evokes the broad array
of responses observed. To date, there is
no high throughput way to relate specific
descending neurons with a given behavior
in flies. A new study remedies this with a
technique to map the function of individual
descending neurons. Using optogenetics,
authors activated individual descending
neurons and then employed an automated
behavior classification system to analyze video
captured data and assign a regulated behavior.
Investigators classified between a third and
a half of all descending neurons. The data
revealed redundancy with many of the
neurons eliciting similar behaviors that were
stereotypical.
CN
https://doi.org/10.1038/s41684-018-0125-5
Genetic engineering
Nat. Biotechnol., https://doi.org/10.1038/nbt.4166
(2018).
PLoS Biol, https://doi.org/10.1371/journal.
pbio.2005086 (2018).
Targetable nucleases have made genetic
engineering of animals for research a
much more tractable endeavor. But,
efficient transfer of large insertion products
remains challenging and inefficient,
despite several recent innovations. To date,
most reported techniques transformed
zygotes for generation of engineered
mouse lines. Authors of a new manuscript
took a different approach and introduced
CRISPR/Cas9 reagents to two-cell zygotes
so as to take advantage of the extended
G2 phase—post-DNA replication and
pre-mitosis—to increase the time during
which recombination could occur.
Investigators also used a streptavidin tagged
Cas9 in combination with a biotinylated
repair template to increase efficient
construct interaction and thereby improve
recombination. With these alterations,
transformation efficiency improved several
fold over conventional methods.
CN
When an organism suffers non-symmetric
damage during development, the
impacted tissue must repair itself and grow
disproportionally quicker in order to regain
proper size and proportions. Authors of a
recent study present a novel model for studying
this process and extend our understanding
of long bone development in fetal mice.
In the report, investigators delivered an
inducible cartilage-specific cell cycle repressor
that blocked cell division in a fraction of
chondrocytes on the left side, leaving the
right side as the control. As compensation,
unmodified left-side chondrocytes increased
proliferation and there was also a net
increase in extracellular matrix deposition.
Interestingly, there was a mild decrease in
systemic growth, which authors speculate was
a result of communication between impacted
chondrocytes and the placenta. Such a decrease
may facilitate the catch-up process.
CN
https://doi.org/10.1038/s41684-018-0124-6
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Playing catch-up
Lab Animal
Identification
https://doi.org/10.1038/s41684-018-0126-4
Ellen P. Neff and Clark Nelson
Lab Animal | VOL 47 | AUGUST 2018 | 207–212 | www.nature.com/laban
209
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