Skip to main content
. Author manuscript; available in PMC: 2023 Dec 12.
Published in final edited form as: Nat Rev Genet. 2022 Nov 23;24(5):276–294. doi: 10.1038/s41576-022-00550-0

Table 1 |.

Interface between RBPs and their effectors

Effector Effector proteina Effector contact regionb RBPa RBP contact regionb Kd (μM)c Process regulated by the RBP-effector interaction
Spliceosome SNRNP70 (U1-70K)d RS domain (IDR) SRSF1/2 (SC35) RS domain (IDR) Pre-mRNA splicing
SNRPA (U1A)d RRM1 domain (SD) SAM68 (KHDRBS1) Y-rich (YY) region (IDR)
SNRPC (U1C)d N terminus (SD) TIA1 Q-rich domain (IDR)
U1 snRNAd SL3 of U1 snRNA FUS RRM domain (SD)
U2AF65 RS domain (IDR) YBX1 Basic/acidic repeats (IDR)
SMN SMN Tudor domain (SD) ELAVL4 (HuD) NR mRNA transport, translation
IGF2BP1 (ZBP1) KH domain region
KHSRP (FUBP2) NR (methylated Arg) (IDR) mRNA stability
FUS RGG box (IDR) and RRM (SD) Pre-mRNA splicing
Tudor domain (SD) and YG box (SD) HNRNPR RGG box (IDR) mRNA transport, pre-mRNA splicing
SYNCRIP RGG box (IDR)
EWSR1 RG domain (IDR) NR
YG box (SD) FMRP Internal segment (IDR) mRNA transport, translation
NR HNRNPU RGG box (IDR) NR
NIRs TNPO1 HEAT repeats (SD) HNRNPA1 PY-NLS SLiM (IDR)e 0.042 Nuclear import, RBP chaperoning/disaggregation
HNRNPA2B1
EWSR1
TAF15
FUS 0.0095
HNRNPF Nuclear import
HNRNPM 0.01
HNRNPD 0.0032
HNRNPDL 1
SAM68 (KHDRBS1)
ELAVL1 (HUR)
KAP104(yeast) Nab2p(yeast) 0.037
Hrp1p(yeast) 0.032
Kapβ1/Impα HEAT/Arm repeats (SD) TDP43 (TARDBP) cNLS SLiM (IDR)e 0.066 Nuclear import, RBP chaperoning/disaggregation
Motor proteins Myo4p(yeast) C terminus (SD) She3p(yeast) Pseudocoiled-coil (SD) 0.058 mRNA transport
She3p-She2p(yeast)f P/R sites (IDR)-structure (SD) 1.6
KIF11 Tail domain (IDR/SD) IGF2BP1 (ZBP1) RRM domains (SD)
KIF3C C terminus (IDR) FMRP NR
UPF1 UPF1 Helicase domain (SD) SLBP N-terminal half (IDR) mRNA stability
RecA domain (SD) and Thr28 (IDR) ZC3H12A (regnase 1) Internal segment (IDR) and RNase domain (SD)
N terminus STAU1/2 Tubulin-binding domain (IDR)
CCR4-NOT CNOT1 HEAT domain (SD) ZFP36 (TTP) SLiM (IDR) 2 mRNA stability, translation
ZFP36L1 (BRF1)
NR TNRC6C (GW182)g W-containing motifs (IDR)
CNOT9 Concave surface (SD) Bam CBM SLiM (IDR) 0.183
RC3H1/2 (Roquin 1/2) mRNA stability
CNOT4 mRNA stability
Convex surface (W pockets) (SD) ZFP36 (TTP) Isolated W residues (IDR) 5.5 mRNA stability
TNRC6A/C (GW182)g mRNA stability, translation
NOT module NR (SD) RC3H1/2 (Roquin 1/2) C terminus (IDR) mRNA stability
HELZ mRNA stability, translation
PUM1/2 N-terminal domain (IDR)
Bicaudal C KH domains (SD)
SHD (SD) NANOS1–3 SLiM (IDR) Translation
YTHDF2 P/Q/N-rich region (IDR) RNA stability
CNOT4 C terminus (IDR) mRNA stability
PABPC PABPC1 MLLE domain (SD) ATXN2 PAM2 SLiM (IDR) 0.7 RBP chaperoning
HELZ NR
NR USP10 26 NR
Multiple domains MKRN1 RQC, translation
PABPC1/4 NR NFX1 mRNA stability
4EHP 4EHP Dorsal surface (SD) Bicoid (Bcd) SLiM (IDR) Translation
NR PKNOX1 (Prep1)
eIF4G TIF4631/2(yeast) C terminus Scd6(yeast) RGG box (IDR)
Khd1(yeast) NR
Internal region Sbp1(yeast) RGG box (IDR)
Internal region and C terminus Npl3(yeast)

CBM, CAF40-binding motif; IDR, intrinsicaLLy disordered region; Kd, dissociation constant; NIR, nuclear import receptor; NLS, nuclear localization sequence; NR, not reported; PABPC, cytoplasmic poly(A)-binding protein; PY-NLS, proline-tyrosine-rich NLS; RBP, RNA-binding protein; RQC, ribosome quality control; RRM, RNA recognition motif; SD, structured domain; SLiM, short linear motif; SMN, survival motor neuron protein; snRNP, small nuclear ribonucleoprotein; STAU, Staufen; TNPO1, transportin 1.

a

Only those direct RBP-effector interactions are listed where a contact region has been mapped in at least one of the interacting proteins. For a fully referenced list of direct and indirect interactions, see Supplementary Table 2. Effectors and RBPs are named by their official gene symbol with text in brackets indicating popular aliases. All interacting proteins are metazoan except for the indicated yeast proteins.

b

IDR (or its part) or SD (or its part) in brackets indicates peptide organization of the contact region in its non-bound state. Where not reported, this information was obtained through modelling of the protein structure using the structure prediction algorithm AlphaFold173.

c

The Kd in most cases pertains to an in vitro interaction between SLiM of an RBP and the interacting effector domain or the full-length effector protein.

d

Part of U1 snRNP.

e

NIRs can also form secondary, low-affinity contacts with other domains of their cargo RBPs5355.

f

Both She2p and She3p are RBPs in contact with the transported mRNA62.

g

TNRC6A-C are paralogous adaptor proteins that recruit CCR4-NOT to microRNA-targeted messages largely via capture of W residues by tandem W pockets present in CNOT9 and AGO (Argonaute) proteins79,174.