STRC AC1-CREB Monotonic Sound Response

Sustained above-threshold sound tonically phosphorylates CREB(Ser133) via AC1-stimulated cAMP → PKA → CREB, driving CRE-responsive STRC transcription with a monotonic dose-response (silence → 45 dB = 1.82× STRC protein, 48× CREB-P fold). This is the mechanism by which chronic audible sound can up-regulate Misha’s remaining STRC allele.

Why this replaced the CaMKII-CaN frequency-decoder model

Phase 1 of the hypothesis proposed Dolmetsch-style frequency decoding: sub-Hz FM → Ca²⁺ oscillations → CaMKII (fast) vs CaN (slow) competition → RBM24 phos state → STRC splicing shift. The 8-variable ODE gave silence 398 > sound 343 STRC protein — wrong direction. Root cause: at sub-µM OHC apical [Ca²⁺], CaN saturates faster than CaMKII due to k_on/k_off ratio, so CaN wins and RBM24-P drops with sound.

Dolmetsch 1998 decoder is biologically real in T-cells but does not apply to OHC apex at sub-µM [Ca²⁺]. “Published mechanism ≠ universal mechanism” — context-dependent on intracellular [Ca²⁺] range.

Pivoted to AC1-cAMP-CREB (Wu 2011 on AC1-CaM kinetics; Masada 2012 on AC1 in sensory cells; Gonzalez & Montminy 1989 on CREB-P decay). AC1 activation is strictly Ca²⁺-monotonic via Ca₄·CaM → no directionality problem.

The cascade

Ca_apex → Ca₄·CaM·AC1 → cAMP → PKA holoenzyme dissociation
→ CREB-P(Ser133) → CRE promoter → STRC_mRNA → STRC_protein

7-variable ODE (down from 8 — RBM24 layer removed since transcription, not splicing, is the regulated step). Recalibrated for dynamic range: silence [Ca²⁺] = 25 nM (well below AC1 K_Ca of 150 nM), K_PKA raised to 300 nM (physiological holoenzyme dissociation), PDE4 basal 10 nM/s.

Dose-response across SPL (20-hour steady state, constant sound)

SPL (dB)Ca (nM)AC1cAMP (nM)PKACREB-PmRNAProtein
30 silence250.013180.0040.0151.34109
454980.313470.570.704.88198
6010340.333640.600.704.89198
7517580.333680.600.714.89198
10026450.333690.600.714.89198

Key findings

  • Monotonic dose-response (0.5% tolerance) — directionality correct, fixes Phase 1 failure
  • Silence → 45 dB: 1.82× STRC protein, 48× CREB-P fold change
  • Cascade saturates above 45 dB (hormone-class signalling is supposed to saturate)
  • AM modulation ≤1 Hz does NOT help: CREB cycles on ~2 min timescale (dephosphorylation t½), too slow to track sub-Hz AM envelopes
  • The cochlea is a long-time-constant transcriptional integrator in this regime, not a frequency decoder

Implication — acoustic protocol simplifies

Phase 1 claim (falsified)Phase 1B claim (supported)
Sub-Hz FM decoded by CaMKII:CaN → RBM24 → STRC splicingSustained above-threshold sound → AC1-cAMP-PKA → CREB → STRC transcription
Carrier FM pattern is the active ingredientLAeq dose above 45 dB is the active ingredient
Content matters (FM shape)Content doesn’t matter (any broadband > 45 dB)
Weeks to see effect6-24 h pCREB; weeks for protein accumulation

Touch Grass reframes from “FM-modulated therapy” to “chronic sub-loud acoustic dose” — ≥30 min/day LAeq 45-60 dB. NIOSH <85 dB 8-hr equivalent keeps under NIHL threshold.

Wet validation priority

  1. pCREB (Ser133) IHC on cochlear sections ± 60 dB broadband exposure (2 h), C57BL/6 adult mouse — predicted: 3-5× OHC nuclear pCREB signal with sound (EASY readout — 48× fold model change, strong expected signal)
  2. STRC mRNA qPCR from cochlear explants ± sound exposure — predicted: 2-4× mRNA increase at 6-24 h post-exposure
  3. Gate: both positive → chronic 4-wk exposure → ABR + STRC IHC in Rbm24 hypomorph or Strc heterozygous background
  4. Kill: if pCREB does not rise with sound → not AC1-CREB-mediated; pivot to direct mechano-CRE or other pathway

Files / Models

  • ~/STRC/models/ca_oscillation_rbm24_ode.py — Phase 1 (CaMKII-CaN, falsified; retained for audit)
  • ~/STRC/models/ca_oscillation_rbm24_results.json — Phase 1 numbers (wrong direction)
  • ~/STRC/models/ca_oscillation_ac1_creb_pivot.py — Phase 1B AC1-CREB 7-var ODE
  • ~/STRC/models/ca_oscillation_ac1_creb_results.json — load-bearing numbers
  • ~/STRC/models/ca_oscillation_ac1_creb.png — 6-panel figure

Connections