Science 13Mar2020

(lily) #1

likely correspond to the RNA-recognition motif
and protein interaction domain of Orb2 (Fig.
4C, gray density). We could identify densities
that correspond to peptide-group oxygen atoms,
ordered solvent molecules in each interface, and
alternative conformations of histidine side
chains(fig.S10,AtoC).Consequently,we
could build and stereochemically refine an
atomic model de novo. The resulting model of
the amyloid core comprised 31 amino acid
residues from the glutamine-rich prion-like
domain of Orb2 (Fig. 4, D and E). Orb2 pro-
tein has two isoforms in the fly brain ( 10 )that


share the prion-like domain but differ in their
N-terminal extension (Fig. 4F). The low-
abundant Orb2A seeds aggregation of preva-
lent Orb2B, which can subsequently seed Orb2B
protein ( 10 ). Of the protein in our sample, 97.5%
is Orb2B (fig. S1C), and the protofilament core
structure extends from residues 176 to 206 of
Orb2B (Fig. 4, D and E).
The protofilament core adopts a simple
hairpin-like fold, composed of twob-strands,
b1(residues176to186)andb2 (residues 197 to
206), with a wide turn (residues 187 to 196) in
between (Fig. 4G). Perpendicular to the helical

axis, a difference in height of 6 Å between the
highest point in the turn and the lowest point
in the tip of theb2 allows an ordered hydrogen-
bonding network of theb-stranded regions
(Fig. 4H). The cross-bpacking of the two
b-strands is made of a tight interdigitation
of glutamine residues, Q179, Q181, Q183, and
Q185 fromb1 and Q200, Q202, and Q204
fromb2 (Fig. 4I). A single leucine, L198, sep-
arates this block of seven glutamines from a
clusteroffourmoreinteriorglutamineresi-
dues in the hairpin turn: Q187, Q190, Q193,
and Q196 (Fig. 4E). Next to H189, there is an

Hervaset al.,Science 367 , 1230–1234 (2020) 13 March 2020 3of5


Fig. 3. Biochemical activity of
Orb2 monomer, oligomer, and
filament isolated from adult head.
(A) Schematic representation of
the biochemical activity of Orb2.
CG13928 binds to Orb2 monomer
and recruit translation repression
complex (indicated in yellow).
CG4612 binds to aggregated Orb2
and recruit translation promoting
complex (indicated in green).
(B) Negative-stain EM of nanogold-
labeled 3′UTR of Tequila mRNA
bound to Orb2 filaments. Black
dots indicated with white arrows
are nanogold particle (~2 nm) attached
to target mRNA. (C) Immuno-EM
of CG4612 bound to Orb2 filaments.
Black dots indicated with black
arrows are gold particles (~6 nm)
attached to CG4612 protein. (D)EM
of Orb2 filaments bound to nanogold-
labeled 3′UTR of Tequila mRNA
and CG4612 protein. The larger
gold particle (~6 nm, black arrows)
represents CG4612 protein, and
the smaller gold particle (~2 nm,
white arrows) represents the mRNA.
(E) Translation of Orb2-target
mRNA in presence of different Orb2
species, obtained from embryo,
adult fly head, or seeding reaction.
Purified Orb2 monomer represses
translation, while Orb2 oligomer
and filament enhance translation. Bovine
serum albumin (BSA) was used as
a control. ***P= 0.0003, ****P<
0.0001; Student’sttest; two tailed.
Data are expressed as mean ± SEM.

AAA AAAAAAA^ AAA^
A A A AAAAA A
A^ AAA AAAAAA

Au
Mono-amino
nanogold

45 min RT

AAAAA

113 bp Tequila
3’UTR mRNA

CGUUGU M2P

UUUUGU Wt

Au-labelled-mRNA

BC

500 Å 500 Å 500 Å 500 Å

gold-labelled anti-CG4612

45 min RT

Au-labelled-
mRNA

500 Å

CG4612 CG4612Δ

Te q 5 ’ Teq 3’

Firefly

60 min RT

AT P
aa Mix

FF/RL
translation extractΔorb2 ratio

SV40 5’ SV40 3’
Renila

E

seeded

D

10x wash

+ Au +

mRNA-binding protein-binding

mRNA and protein-binding

A A
A

Orb2
Ribosomemonomer
PolyA tail

CG13928

A A
A
A A A

Ribosome filamentOrb2

PolyA tail

Translation
repression

Translation
activation

A

100 Å 100 Å

100 Å

Wt mRNA-Orb2 filament M2P mRNA-Orb2 filament CG4612-Orb2 filament CG4612Δ-Orb2 filament

Wt mRNA-CG4612-Orb2 filament M2P-CG4612Δ-Orb2 filament

CG4612

A

500

400

300

200

100

0

120

80

60

40

20

0

100

***

****

BSA
seeded seeded

BSA

Repression
complex CGG Activationcomplex

Rib Rib RibRiRiRib

A (^) A
A A
G46
(^) AA
46
(^) A AAAAAAAAA A AAAA A A AAAAAA
C CCCC
A A
A
A AA
A AAA
....
.
.
....
..
% Normalized FF/RL
or
or
Au
30 min RT, 30 min 4°C
CG4612 CG4612Δ





    • gold-labelled
      anti-CG4612





    • 10x wash
      M2P
      Wt
      M2P
      Wt




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